id
stringlengths 10
11
| text
stringlengths 0
185k
| title
stringlengths 0
273
| date
stringlengths 0
10
| authors
stringlengths 0
356
| language
stringclasses 2
values |
---|---|---|---|---|---|
PMC6021049 |
1
Table A. Linear mixed-effect model results for transformed minimum reaction
times for all sprints in 2016.
(...TRUNCATED) | On the apparent decrease in Olympic sprinter reaction times.(...TRUNCATED) | 06-27-2018 | Mirshams Shahshahani, Payam,Lipps, David B,Galecki, Andrzej T,Ashton-Miller, James A(...TRUNCATED) | eng |
PMC10688325 | Supplementary File 3: P-values of the Wilcoxon-Mann-Whitney tests assessing the null
hypothesis that it is equally likely that a value chosen at random from one year is greater or less
than a value chosen at random from another year’s population.
Top 100
Table 1 Men’s 100m
Table 2 Men‘s 110m hurdles
Table 3 Men‘s 200m
Table 4 Men‘s 400m
Table 5 Men‘s 400m hurdles
2016
2017
2018
2019
2021
2017
1
2018
1 0.638283
2019
1
1
1
2021
1 0.309905
1
1
2022
1
0.00015
0.00196 0.003115 0.062573
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1 0,714507
2021 0,097206
0,025 0,000356 0,003474
2022 0,003464 0,000552
4,56E-06
3,78E-05 0,726513
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1
1
1
1
2022 0,052459 0,001119 0,046565 0,014442 0,047502
2016
2017
2018
2019
2021
2017
1
2018 0,572175
1
2019
1
1
1
2021
1
1
1
1
2022 0,052919 0,627806
1 0,078112 0,272402
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1
1
1
1
2022 0,972897
1
1 0,388271 0,973264
Table 6 Women‘s 100m
Table 7 Women‘s 100m hurdles
Table 8 Women‘s 200m
Table 9 Women‘s 400m
Table 10 Women‘s 400m hurdles
2016
2017
2018
2019
2021
2017
1
2018
1 0,466331
2019
1
1
1
2021
0,03227
0,02574 0,139897 0,011156
2022
4,53E-07
4,06E-06
2,3E-06
4,28E-08 0,003582
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1 0,004164 0,065499 0,129516
2022 0,746016 0,001377 0,023704 0,042453
1
2016
2017
2018
2019
2021
2017
1
2018
1 0,492091
2019
1
1
1
2021
1 0,265376
1 0,002601
2022 0,085241 0,000304 0,043264
2,27E-06 0,265376
2016
2017
2018
2019
2021
2017
1
2018 0,804407 0,371019
2019
1 0,702147
1
2021
1,35E-05
2,2E-07 0,001172
6,98E-05
2022
4,93E-05
5,75E-07 0,002364 0,000161
1
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1
1 0,346209 0,375669
2022
1 0,608207 0,098102 0,080571
1
Top 20
Table 11 Men‘s 100m
Table 112 Men‘s 110m hurdles
Table 13 Men‘s 200m
Table 14 Men‘s 400m
Table 15 Men‘s 400m hurdles
2016
2017
2018
2019
2021
2017
1
2018
1 0,800315
2019
1
1
1
2021 0,972321 0,017573 0,297023 0,059996
2022
1 0,021544
0,33573 0,078011
1
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021 0,303898
0,57473 0,003671 0,082601
2022 0,109341 0,290332 0,003215 0,062877
1
2016
2017
2018
2019
2021
2017
1
2018
1 0,062617
2019
1 0,175687
1
2021
1 0,685787
1
1
2022 0,175687 0,000813 0,232567 0,269417 0,154942
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1
1
1
1
2022
1
1
1
1
1
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021 0,407642 0,524398
0,53255 0,160764
2022 0,197812 0,338821 0,407642 0,160764
1
Table 16 Women‘s 100m
Table 17 Women‘s 100m hurdles
Table 18 Women‘s 200m
Table 19 Women‘s 400m
Table 20 Women‘s 400m hurdles
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1 0,517847 0,006641 0,012547
2022 0,317904 0,018162
4,46E-05 0,004229 0,494987
2016
2017
2018
2019
2021
2017 0,711735
2018
1
1
2019 0,711735
1 0,699526
2021 0,045484 0,231794 0,114568 0,614191
2022 0,001485 0,001485 0,005646 0,014589 0,076741
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021 0,012536 0,016489 0,003203 0,007309
2022 0,007309 0,007309 0,001137 0,005665
1
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021 0,026829 0,011861 0,054195 0,010109
2022 0,467379 0,615339 0,757428 0,054195
1
2016
2017
2018
2019
2021
2017
1
2018
1
1
2019
1
1
1
2021
1
1 0,074017 0,574967
2022 0,103321 0,574967 0,005963 0,074017
1
(...TRUNCATED) | The potential impact of advanced footwear technology on the recent evolution of elite sprint performances.(...TRUNCATED) | 11-27-2023 | Mason, Joel,Niedziela, Dominik,Morin, Jean-Benoit,Groll, Andreas,Zech, Astrid(...TRUNCATED) | eng |
PMC5325470 | RESEARCH ARTICLE
Comparison of wrist-worn Fitbit Flex and
waist-worn ActiGraph for measuring steps in
free-living adults
Anne H. Y. Chu1*, Sheryl H. X. Ng1, Mahsa Paknezhad2, Alvaro Gauterin2, David Koh1,3,
Michael S. Brown4, Falk Mu¨ller-Riemenschneider1,5
1 Saw Swee Hock School of Public Health, National University of Singapore, Singapore, Singapore,
2 Department of Computer Science, School of Computing, National University of Singapore, Singapore,
Singapore, 3 PAPRSB Institute of Health Sciences, Universiti Brunei Darussalam, Jalan Tungku Link,
Gadong, Brunei Darussalam, 4 Department of Electrical Engineering and Computer Science, Lassonde
School of Engineering, York University, Toronto, Ontario, Canada, 5 Institute of Social Medicine,
Epidemiology and Health Economics, Charite´ University Medical Centre Berlin, Berlin, Germany
* [email protected], [email protected]
Abstract
Introduction
Accelerometers are commonly used to assess physical activity. Consumer activity trackers
have become increasingly popular today, such as the Fitbit. This study aimed to compare
the average number of steps per day using the wrist-worn Fitbit Flex and waist-worn Acti-
Graph (wGT3X-BT) in free-living conditions.
Methods
104 adult participants (n = 35 males; n = 69 females) were asked to wear a Fitbit Flex and an
ActiGraph concurrently for 7 days. Daily step counts were used to classify inactive (<10,000
steps) and active (10,000 steps) days, which is one of the commonly used physical activity
guidelines to maintain health. Proportion of agreement between physical activity categoriza-
tions from ActiGraph and Fitbit Flex was assessed. Statistical analyses included Spear-
man’s rho, intraclass correlation (ICC), median absolute percentage error (MAPE), Kappa
statistics, and Bland-Altman plots. Analyses were performed among all participants, by
each step-defined daily physical activity category and gender.
Results
The median average steps/day recorded by Fitbit Flex and ActiGraph were 10193 and
8812, respectively. Strong positive correlations and agreement were found for all partici-
pants, both genders, as well as daily physical activity categories (Spearman’s rho: 0.76–
0.91; ICC: 0.73–0.87). The MAPE was: 15.5% (95% confidence interval [CI]: 5.8–28.1%) for
overall steps, 16.9% (6.8–30.3%) vs. 15.1% (4.5–27.3%) in males and females, and 20.4%
(8.7–35.9%) vs. 9.6% (1.0–18.4%) during inactive days and active days. Bland-Altman plot
indicated a median overestimation of 1300 steps/day by the Fitbit Flex in all participants.
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
1 / 13
a1111111111
a1111111111
a1111111111
a1111111111
a1111111111
OPEN ACCESS
Citation: Chu AHY, Ng SHX, Paknezhad M,
Gauterin A, Koh D, Brown MS, et al. (2017)
Comparison of wrist-worn Fitbit Flex and waist-
worn ActiGraph for measuring steps in free-living
adults. PLoS ONE 12(2): e0172535. doi:10.1371/
journal.pone.0172535
Editor: Maciej Buchowski, Vanderbilt University,
UNITED STATES
Received: August 18, 2016
Accepted: February 6, 2017
Published: February 24, 2017
Copyright: © 2017 Chu et al. This is an open
access article distributed under the terms of the
Creative Commons Attribution License, which
permits unrestricted use, distribution, and
reproduction in any medium, provided the original
author and source are credited.
Data Availability Statement: Due to ethical
restrictions set by the National University of
Singapore Institutional Review Board, study data
cannot be made publicly available. Requests for
data may be sent to Anne Chu (email: anne.chu@u.
nus.edu), Falk Mu¨ller-Riemenschneider (email:
[email protected]) or the National University of
Singapore Institutional Review Board (email:
[email protected]).
Fitbit Flex and ActiGraph respectively classified 51.5% and 37.5% of the days as active
(Kappa: 0.66).
Conclusions
There were high correlations and agreement in steps between Fitbit Flex and ActiGraph.
However, findings suggested discrepancies in steps between devices. This imposed a chal-
lenge that needs to be considered when using Fibit Flex in research and health promotion
programs.
Introduction
New wearable technologies have helped raise individual self-awareness about physical activity
behavior. Among all the functionalities that a range of wearable devices have, step counting is
the most fundamental and consistently found feature. Step counts have been proposed as a
health indicator for population studies [1], and even community-based health-promotion pro-
grams [2]. The 10,000 steps/day guideline is one of the commonly used physical activity indices
[3]. Various government/professional organizations around the world have used the 10,000
daily steps recommendation as an index of high physical activity level. This daily step-based rec-
ommendation has been endorsed by the World Health Organization (WHO), National Heart
Association of Australia, US Centers for Disease Control and Prevention, and American Heart
Association to improve overall health. For healthy adults, it appears that this guideline is a real-
istic estimate of an appropriate daily physical activity level [4, 5]. It was suggested that those
achieving the goal of 10,000 steps per day were more likely to meet physical activity guidelines
as compared to those with lower step counts [2]. Furthermore, health promotion programs that
included a daily step goal were reportedly more successful in increasing physical activity than
those without this component [6]. The use of step data (usually as steps/day) is a simple means
of reflecting habitual physical activity pattern, and this approach has become acceptable to
many researchers and practitioners [1, 6]. Moreover, walking activity has been reported as a
prevalent form of leisure-time physical activity and a functional task in the daily lives [7].
Among all the accelerometers commonly used in research, the ActiGraph (Pensacola, FL,
USA) is well-validated and has been extensively used for assessing physical activity under free-
living conditions [8–11]; The ActiGraph accelerometers use algorithms to quantify and con-
textualize the resultant acceleration signals of human motion. They have shown high accuracy
for moderate-to-high walking speed stepping in the laboratory (compared to direct observa-
tions, ICC: 0.72–0.99) and under free-living conditions (compared to the Yamax Digiwalker,
ICC: 0.90) [12]. The ActiGraph has been used in large-scale epidemiological studies such as
the US National Health and Nutrition Examination Survey (NHANES) [13], and the Women’s
Health Study (WHS) [14].
Recently, consumer-based activity trackers (e.g. Fitbit, Jawbone UP, LUMOback, Nike
+ Fuelband, Omron Walking Style Pro pedometer, etc.) and in-built accelerometers in smart-
phones have become increasingly popular [15, 16]. It was forecasted that the smart wearables
market could reach 170 million units by 2017 [17]. Fitbit (San Francisco, CA, USA) is one of
the most commonly used brands amongst the consumer-based activity trackers. As of 2015,
Fitbit had reached 9.5 million active users [18]. Among their products, the wrist-worn Fitbit
Flex has become popular in recent years either for aesthetic reasons or wearing comfort. The
Fitbit Flex is sleek and displays only LED with a tap screen. Users are able to monitor and
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
2 / 13
Funding: This research was supported by a grant
WBS: R-608-000-117-646 from the National
University of Singapore.
Competing interests: The authors have declared
that no competing interests exist.
access data on the number of steps, sleep quality, and other personal metrics through the Fitbit
dashboard. This could be useful for targeted physical activity interventions designed to achieve
healthy behaviors. It was suggested that wrist-worn accelerometers allowed for monitoring of
low-intensity activities, and were associated with considerable increases in wearing compliance
and data quality [19].
A number of studies have validated wireless consumer-based monitors of different brands
in measuring step counts and energy expenditure [16, 20–23]. A recent systematic review con-
cluded high validity for the Fitbit Classic, One and Zip compared to accelerometry-based step
counts (particularly in laboratory settings) [24]. It was further highlighted that more field-
based studies are needed. Evaluation of the trackers in assessing free-living physical activity
(non-controlled environment outside a lab setting) is particularly important, as the results are
more likely to reflect usual day-to-day activities. To date, sample sizes of studies on the Fitbit
Flex validity under free-living conditions have been relatively small (ranging from 14 to 25 par-
ticipants) and based on young adults [16, 25–27]. Of note, one similar study was limited by a
small sample size of one adult only [28]. However, despite the high correlation between activity
trackers, these studies generally showed that Fitbit Flex has measurement limitations regarding
the overestimation and underestimation of activity levels compared with the reference device,
depending on different study settings and types of activity [26, 27].
Given these considerations and highlighted gaps, this study aimed to make standardized
comparisons based on step counts from the consumer-oriented Fitbit Flex and the research-
grade ActiGraph wGT3X-BT. Differences in levels and types of physical activity between
males and females have been reported [29, 30]. It was reported that more males than females
tended to practise sports (e.g. soccer, basketball, etc.), whereas females were more likely to
engage in yoga, dancing, aerobics, etc. [31]. Because these differences may influence their accu-
racy in measurement, we further performed gender specific analysis. Hence, the objectives of
this study were:
1. To compare free-living steps/day recorded by the Fitbit Flex and the ActiGraph wGT3X-BT
accelerometers in all participants, by each step-defined daily physical activity category and
gender.
2. To compare the agreement between devices in classifying participants’ step-defined daily
physical activity categories.
Materials and methods
Study design and participants
This was a cross-sectional study. The present study was a part of a previously published study
[32], whereby a convenience sample of 107 employees who completed both ActiGraph and Fit-
bit Flex measures were included. Participants from a large public University and a hospital in
Singapore were recruited between February 2014 and June 2014. Individuals were residing in
Singapore and were of various ethnicities (Chinese, Malay, Indian and others). Participants
were invited to take part in this study through mass e-mailing. Individuals who indicated inter-
est were approached and interviewed by the researcher.
The inclusion criteria were:
1. Males and females aged 21 to 65 years
2. Either students or working adults
3. Absence of physical disabilities or illness that would create abnormal gait patterns.
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
3 / 13
The study was approved by the National University of Singapore Institutional Review
Board (NUS-IRB Ref No.: B-14-021). Participants provided their written informed consent to
participate in this study.
Procedure
The goals and procedures of the study were explained to each participant by the researcher via
face-to-face interview. Participants’ information on gender, age, education level, height and
weight were self-reported. Instructions were given to the participants by trained personnel on
how to put on a wrist-worn Fitbit Flex and a waist-worn ActiGraph concurrently for 7 days.
Instruction manuals on the proper use of the ActiGraph and Fitbit Flex were also given to par-
ticipants for additional guidance. Participants were instructed that the devices had to be worn
for at least 10 hours/day, and could be removed at night depending on their comfort level.
They were asked to complete a daily time sheet to record each wearing day when both devices
were worn while maintaining their normal activities. Information required on the time sheet
comprised of the dates they started and stopped wearing the devices.
ActiGraph wGT3X-BT
The ActiGraph™ wGT3X-BT monitor (ActiGraph, LLC, Pensacola, Florida, USA) is a triaxial
accelerometer (Dimensions: 4.6cm x 3.3cm x 1.5cm; weight: 19 grams) worn on the waist
using an elastic belt to secure above the right hip bone for quantifying the amount and fre-
quency of human movements. The monitor was initialized at a sample rate of 30Hz to record
activities for free-living conditions. Participants were instructed to wear the ActiGraph for
7-day. They were allowed to remove the ActiGraph only while bathing or immersing the body
in water. ActiGraph data were downloaded using ActiLife 6 software (ActiGraph, LLC, Pensa-
cola, FL, USA) by the researchers upon collection of the devices. Downloaded data were inte-
grated into 60-sec epochs.
Fitbit Flex
Fitbit FlexTM (Dimensions: 22.2cm x 6.0cm x 6.0cm; weight: 100 grams) is a wrist-worn wear-
able wireless sensor with a triaxial accelerometer that records physical activity throughout the
day. It can sync with a smartphone application/computer. Participants were instructed to wear
the Fitbit Flex on their non-dominant wrist, for the same duration as the ActiGraph (up to
7-day) concurrently. In general, Fitbit Flex requires the creation of individual user accounts to
download stored data using a Web-based software application. However, for the purpose of
our study, anonymous user accounts were created by the study team which could only be
accessed by the researchers. Steps data were therefore stored on the devices, and the minute-
by-minute Fitbit Flex data were downloaded at the end of each participant’s wearing period by
the study team.
Data reduction
For wear time validation, because the ActiGraph accelerometer is an established device to mea-
sure physical activity with many validation studies determining their accuracy [33, 34], valid
wear time determined by the ActiGraph was regarded as the reference. A detailed description
of the procedures on ActiGraph wear time validation and removal of sleep time can be found
elsewhere [32]. Then, a valid day was defined as having an accumulation of 1500 steps/day
with 10 hours/day restricted only to common wear time based on both ActiGraph and Fitbit
Flex. The 1500 steps/day criterion was based on a previous research conducted by Tudor-
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
4 / 13
Locke et al. comparing accelerometers positioned at different locations under free-living con-
ditions [35]. All participants with 4 valid days of data were included in the analysis. Addi-
tionally, wear time was also verified based on the daily time sheets.
Statistical analysis
All statistical procedures were performed using SPSS software (version 20.0). The significance
level was set at P<0.05. Descriptive characteristics were presented as mean (standard devia-
tion; SD) or median (interquartile range; IQR). Shapiro-Wilk test was used to determine
whether the data was normally distributed. Differences in the characteristics between genders
were detected by non-parametric tests. Mann-Whitney U test (for continuous variables), chi-
squared test (for categorical variables) and Fisher’s exact test (for categorical variables with
cells having an expected frequency of five or less) were used.
Analyses of the relationship between ActiGraph and Fitbit Flex were performed across: all
participants, by each category of step-defined daily physical activity, and gender. Because there
could be potential within-subject variations, comparison of step counts for the magnitude of
relationship between the two devices was done on a day-to-day basis. Spearman’s correlation
coefficient (rho) and intraclass correlation coefficient (ICC) were used to assess correlation
and agreement, respectively in steps between ActiGraph and Fitbit Flex. An ICC value of
0.75 implied excellent, 0.60–0.74 good, 0.40–0.59 fair and <0.40 poor agreement [36].
Median of absolute percentage error (MAPE) between devices was calculated: (absolute error/
observed steps) × 100%. The difference in MAPE by each category of step-defined daily physi-
cal activity and gender was compared using Mann-Whitney U test. ActiGraph derived steps/
day was used to classify two step-defined activity categories for the assessments of Spearman’s
rho and ICC. The classification of days into two step-defined activity categories was adapted
based on previous studies: valid days with a cumulative of 10,000 steps/day were considered
as active days, and <10,000 steps/day were inactive days [5, 37, 38]. As for the Bland-Altman
analysis, a non-parametric approach was adopted since the differences between the two devices
were non-normally distributed. Bland-Altman plots were presented as median, 10th and 90th
percentiles to display variance around differences between two devices. Proportion of agree-
ment in achievement of 10,000 steps per day produced by ActiGraph and Fitbit Flex was
assessed using Kappa.
Results
Out of 107 recruited participants, 104 were included because they met the wear time criteria
and provided 682 days of data. Table 1 shows participants’ sociodemographic characteristics of
the study. Participants had a median age of 31.0 years (IQR: 26.0–42.8), predominantly female
(66.3%), and had a university degree (74.0%). On average, 6.6 valid wear days were recorded
per participant and there was no significant difference between males and females. The Acti-
Graph and Fitbit Flex steps were significantly higher in males than females (P = 0.03 and 0.01
for ActiGraph and Fitbit Flex, respectively).
Fitbit Flex recorded a significantly higher (P < 0.001) number of daily step counts than that
from the ActiGraph across all participants, by gender and each category of step-defined daily
physical activity (Table 2). Males reflect significantly higher daily step counts from Fitbit Flex
(P = 0.01) and ActiGraph (P = 0.028) compared to females.
The magnitude of the correlation and agreement in step counts between ActiGraph and Fit-
bit Flex were assessed (Table 2). Good to excellent significant positive correlations and agree-
ment were shown in all participants, by gender and category of step-defined daily physical
activity. Table 3 shows the number of days that were misclassified as active or inactive
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
5 / 13
according to the Fitbit Flex. The proportion of overall agreement of devices in classifying days
as active or inactive was estimated, reporting a kappa of 0.66, indicating a moderate agreement
(Table 3).
Fig 1 shows the MAPE in number of steps between the two devices. Significant differences
in the MAPE of step counts were found between devices across step-defined physical activity
categories (P<0.001), but not for gender (P = 0.17).
Figs 2 and 3A–3D present Bland-Altman plots on the median of differences, and the 10th
and 90th percentiles between steps/day obtained from Fitbit Flex and ActiGraph. The bias
(median difference) is 1300 steps/day for all participants. In general, the Fitbit Flex overesti-
mated steps/day relative to ActiGraph (median differences range: 1166–1509 steps/day by gen-
der and 1280–1312 by step-defined physical activity categories).
Discussion
This study focused on the direct comparison of steps obtained from the Fitbit Flex and Acti-
Graph. The results show positive correlations and agreement in step counts of free-living
adults as measured by the waist-worn ActiGraph and wrist-worn Fitbit Flex activity monitors.
At the same time, overestimation of step counts and classification as active days by Fitbit Flex
were found. This may have important public health implications if consumers or participants
of health promotion programs are identified as being active when in fact they are not.
Table 1. Characteristics of study population.
All (n = 104)
Males (n = 35)
Females (n = 69)
P-valuea
Age (Med; IQR)
31.0; 26.0–42.8
33.0; 27.0–50.0
30.0; 25.5–40.5
0.05
Height, cm (Med; IQR)
163.0; 157.0–169.8
170.0; 168.0–175.0
160.0; 155.0–163.0
<0.001
Weight, kg (Med; IQR)
60.0; 53.0–69.9
65.0; 60.0–80.0
56.6; 50.0–66.0
<0.001
BMI (Med; IQR)
22.6; 20.3–25.5
23.1; 20.8–25.8
22.1; 20.2–25.1
0.3
Education, n (%)
0.01
Secondary
7 (6.8)
0 (0)
7 (10.2)
Technical school/diploma
20 (19.2)
3 (8.6)
17 (24.6)
University
77 (74.0)
32 (91.4)
45 (65.2)
Organization, n (%)
0.51
Public university
70 (67.3)
24 (68.6)
46 (66.7)
University hospital
34 (32.7)
11 (31.4)
23 (33.3)
0.92
Valid wearing day/week (M±SD)
6.6 ± 0.9
6.6 ± 1.0
6.5 ± 0.9
BMI, body mass index; IQR, interquartile range; M, mean; Med, median; SD standard deviation.
a Test of significant difference between males and females.
doi:10.1371/journal.pone.0172535.t001
Table 2. Comparison, relative agreement and median of absolute error in step counts between ActiGraph and Fitbit Flex: all participants, by gen-
der and category of step-defined daily physical activity.
Step count/day
All (682 days)
Males (229 days)
Females (453 days)
Inactive (426 days)
Active (256 days)
Fitbit Flex (Med; IQR)
10193; 7490–12898a
11030; 7604–14838a
9992; 7397–12509a
8235; 6267–10003a
14075; 11948–16864a
ActiGraph (Med; IQR)
8812; 6152–11471a
9409; 6268–12897a
8599; 6053–11118a
6856; 4982–8465a
12716; 11112–14505a
Spearman’s rho
0.89*
0.91*
0.87*
0.76*
0.76*
ICC (95% CI)
0.85 (0.58–0.93)
0.87 (0.56–0.94)
0.83 (0.56–0.92)
0.73 (0.68–0.77)
0.82 (0.77–0.85)
CI, confidence interval; IQR, interquartile range.
a ActiGraph and Fitbit Flex estimates are significantly different (P < 0.05).
* P < 0.01
doi:10.1371/journal.pone.0172535.t002
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
6 / 13
Recently, a number of studies have investigated the accuracy of various consumer-based
physical activity trackers, recognizing the role they may play in physical activity promotion.
For instance, Case et al. [16], Storm et al. [20], and Diaz et al. [21] have validated consumer
wearables for measuring steps. However, to date very few studies have investigated the accu-
racy of these monitors under free-living conditions [24]. This is highly important because the
accuracy of devices may differ considerably in day-to-day life as compared to under highly
controlled and short protocols of activities. Recently, several studies have been conducted with
regard to this important research question [25–27]. Dierker et al. [25] assessed the validity of
Fitbit Flex among 17 college-aged adults and found that although the steps measured by Fitbit
Flex (9596 ± 2361 steps) were higher than the ActiGraph GT3X+ (7766 ± 2388 steps), the dif-
ference was not statistically significant (P = 0.052). However, the authors instructed the partici-
pants to remove the devices while they were exercising over the 7-day monitoring period;
hence it is possible that not all free-living movements have been captured as in the present
Table 3. Agreement between ActiGraph and Fitbit Flex for categorizing step-defined daily physical
activity.
No. of days (%)a
ActiGraph
Fitbit Flex
Inactive
Active
Inactive
320 (46.9)
11 (1.6)
Active
106 (15.5)
245 (35.9)
Total
426 (62.5)
256 (37.5)
Kappa (95% CI)
0.66 (0.61–0.71)
a Physical activity categories are based on ActiGraph daily step counts: inactive <10,000 steps/day and
active 10,000 steps/day [5].
doi:10.1371/journal.pone.0172535.t003
Fig 1. MAPE (%) between ActiGraph and Fitbit Flex. Error bars indicate IQR of MAPE. MAPE, median absolute percentage error.
doi:10.1371/journal.pone.0172535.g001
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
7 / 13
study. In another study by Dominick et al. [26], the Fitbit Flex registered a total of 10286 ±
3760 free-living steps/day as compared to the ActiGraph of 9639 ± 3456 steps/day (albeit no
significant difference was found between devices) among 19 participants. In contrast, Sus-
hames et al. [27] reported a larger absolute difference of over 3000 steps (47.0%) in free-living
steps between Fitbit Flex and ActiGraph among 25 adults, of which the Fitbit Flex has underes-
timated step counts. The reason for this underestimation from Fitbit Flex is unclear, but it
could be related to the variability in participants’ movements or undercounting of steps by the
Fitbit Flex.
Different study settings and reference methods could contribute to the discrepancies in out-
comes. Kooiman et al. [39] assessed the validity of Fitbit Flex over 1 day in a smaller sample of
free-living adults and found high agreements in steps with the activPAL. They found a notice-
ably smaller mean absolute percentage difference of 3.7% against the activPAL [39]. In accor-
dance with our findings, another recent study comparing Fitbit Flex and ActiGraph on 48
cardiac patients (mean age: 65.5 years), in which high correlations and a difference in step
counts of 1038 steps/day in the total population over 4 days of monitoring period were
reported. Thus, comparing findings among different populations can provide an implication
Fig 2. Bland-Altman plot of differences between waist-worn ActiGraph and wrist-worn Fitbit Flex against the mean
according to all participants. The solid line represents median of the differences between devices, dotted lines are 10th and
90th percentiles of the differences.
doi:10.1371/journal.pone.0172535.g002
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
8 / 13
of how reproducible and valid this device is. It was also noted that the overestimation in step
counts by the Fitbit Flex in this study resulted in a considerable misclassification of days as
being active, which may have important public health implications. As shown in our analysis,
the differences in steps between Fitbit Flex and ActiGraph were larger on inactive days as com-
pared to active days.
Hypothetically, as most lifestyle activities include movements at the wrist, people might
have performed movements such as hand waving that could be identified as potential false pos-
itive events/steps by Fitbit Flex. It was apparent that wrist-movements could reflect arm/
Fig 3. Bland-Altman plots of differences between waist-worn ActiGraph and wrist-worn Fitbit Flex against the mean according to: (A) Males, (B)
Females, (C) Inactive days, and (D) Active days. The solid lines represent median of the differences between devices, dotted lines are 10th and 90th
percentiles of the differences.
doi:10.1371/journal.pone.0172535.g003
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
9 / 13
forearm motions with a relatively small mass (while sitting), or they could be classified as step
counts (while walking or running) [40]. Tudor-Locke et al. [35] found a large difference even
using the same ActiGraph device placed between different attachment sites. They further
reported that the difference between mean steps from the wrist and waist was 2558 steps under
free-living conditions, with a higher average step counts on the wrist [35]. In line with this,
Hilderbrand et al. [41] found a 200% higher step activity from the wrist-worn GENEActiv
than the waist-worn ActiGraph in some adults. These observations suggest room for further
progress, since recent studies reported using wrist-worn monitors resulted in improved wear-
ing compliance due to comfort issues and without having the need to remove them intermit-
tently [42]. Ultimately, prolonged wear time would improve data quality as the issue of
missing data due to non-compliance could be minimized.
Strengths
Despite the growing body of evidence, this study expands substantially on previous studies. Most
importantly, as highlighted earlier, the comparison of the devices was done under free-living
conditions for estimation of unstructured lifestyle activities. Secondly, the relationship between
these devices were assessed for 7-day of wearing protocol. Thirdly, this study was conducted
among a relatively large sample of adults. Fourthly, the performance of the devices was compared
across different subgroups (males vs. females and step-defined physical activity categories).
Limitations
This study may have limited generalizability as participants were predominantly females, rela-
tively young and healthy. Furthermore, the use of ActiGraph as the reference instrument has
its drawbacks. It is possible that the difference in steps between devices could be attributable to
not only the Fitbit Flex, but also the ActiGraph, which is not the gold standard for measuring
step counts [43]. However, the ActiGraph has been shown to be a valid tool to assess step
count (as compared with the Omron pedometer and Yamax Digiwalker [11, 12]), and it is
practical for use in epidemiological studies [44]. Careful consideration should also be given to
the effects of movement artefact and signal noise due to the use of devices that are not attached
directly to the skin (i.e. Fitbit Flex worn on a wrist-band and ActiGraph on a waist-belt),
which might have affected the devices’ functionality to accurately measure step count. Being
limited to only step count data, there was no indication as to whether the activities performed
were of light-, moderate- or vigorous-intensity level. In general, step counts from accelerome-
ters of different attachment sites (i.e. wrist- and waist-worn) might not be ideal for a direct
comparison; nonetheless, results of this study were more likely to reflect the performances of
these devices in real-world practice.
Conclusions
Positive correlation and agreement in step counts were found between wrist-worn Fitbit Flex
and waist-worn ActiGraph in free living adults, which is consistent with the existing evidence
mainly from laboratory studies. However, a considerable overestimation of Fitbit Flex was
noted, which resulted in substantial misclassification by Fitbit Flex when applying common
step count recommendations. This can have important practical implications for the use of
these devices by researchers, practitioners and health promoters, which often use the achieve-
ment of certain step count goals or increases in step counts as desired outcomes. Evidence pre-
sented in this paper adds to the existing literature on the validity of consumer devices for
physical activity monitoring and these cautionary limitations should be considered in the
design of study data collection and health promotion strategies.
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
10 / 13
Acknowledgments
We thank our colleagues and participants for their involvement in this study.
Author Contributions
Conceptualization: AC FMR.
Data curation: AC FMR AG.
Formal analysis: AC FMR SN AG.
Funding acquisition: FMR.
Investigation: AC FMR.
Methodology: AC FMR SN.
Project administration: AC FMR.
Resources: AC FMR MSB MP AG.
Software: AC FMR SN AG MSB.
Supervision: FMR DK.
Validation: AC FMR.
Visualization: AC.
Writing – original draft: AC FMR SN DK.
Writing – review & editing: AC FMR SN DK.
References
1.
Tudor-Locke C, Johnson WD, Katzmarzyk PT. Accelerometer-determined steps per day in US adults.
Med Sci Sports Exerc. 2009; 41(7):1384–91. doi: 10.1249/MSS.0b013e318199885c PMID: 19516163
2.
Shephard RJ, Tudor-Locke C. The objective monitoring of physical activity: Contributions of accelero-
metry to epidemiology, exercise science and rehabilitation. Cham: Springer; 2016.
3.
Tudor-Locke C, Craig CL, Brown WJ, Clemes SA, De Cocker K, Giles-Corti B, et al. How many steps/
day are enough? For adults. Int J Behav Nutr Phys Act. 2011; 8:79. doi: 10.1186/1479-5868-8-79
PMID: 21798015
4.
Hardman AE, Stensel DJ. Physical activity and health: The evidence explained. 2nd ed. London: Rout-
ledge Taylor and Francis Group; 2009.
5.
Tudor-Locke C, Bassett DR Jr. How many steps/day are enough? Preliminary pedometer indices for
public health. Sports Med. 2004; 34(1):1–8. PMID: 14715035
6.
Bravata DM, Smith-Spangler C, Sundaram V, Gienger AL, Lin N, Lewis R, et al. Using pedometers to
increase physical activity and improve health: a systematic review. JAMA. 2007; 298(19):2296–304.
doi: 10.1001/jama.298.19.2296 PMID: 18029834
7.
Tudor-Locke C, Ham SA. Walking behaviors reported in the American Time Use Survey 2003–2005.
JAMA. 2008; 5(5):633–47.
8.
Calabr MA, Lee JM, Saint-Maurice PF, Yoo H, Welk GJ. Validity of physical activity monitors for assess-
ing lower intensity activity in adults. Int J Behav Nutr Phys Act. 2014; 11(1):1–9.
9.
Aadland E, Ylvisåker E. Reliability of the Actigraph GT3X+ accelerometer in adults under free-living
conditions. PloS One. 2015; 10(8):e0134606. doi: 10.1371/journal.pone.0134606 PMID: 26274586
10.
Freedson P, Bowles HR, Troiano R, Haskell W. Assessment of physical activity using wearable moni-
tors: recommendations for monitor calibration and use in the field. Med Sci Sports Exerc. 2012; 44(1
Suppl 1):S1–4.
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
11 / 13
11.
Rosenberger ME, Buman MP, Haskell WL, McConnell MV, Carstensen LL. 24 Hours of sleep, seden-
tary behavior, and physical activity with nine wearable devices. Med Sci Sports Exerc. 2016; 48(3):457–
65. doi: 10.1249/MSS.0000000000000778 PMID: 26484953
12.
Lee JA, Williams SM, Brown DD, Laurson KR. Concurrent validation of the Actigraph GT3X+, Polar
Active accelerometer, Omron HJ-720 and Yamax Digiwalker SW-701 pedometer step counts in lab-
based and free-living settings. J Sports Sci. 2015; 33(10):991–1000. doi: 10.1080/02640414.2014.
981848 PMID: 25517396
13.
Troiano RP, Berrigan D, Dodd KW, Masse LC, Tilert T, McDowell M. Physical activity in the United
States measured by accelerometer. Med Sci Sports Exerc. 2008; 40(1):181–8. doi: 10.1249/mss.
0b013e31815a51b3 PMID: 18091006
14.
Lee IM, Shiroma EJ. Using accelerometers to measure physical activity in large-scale epidemiologic
studies: issues and challenges. Br J Sports Med. 2014; 48(3):197–201. doi: 10.1136/bjsports-2013-
093154 PMID: 24297837
15.
Fanning J, Mullen SP, McAuley E. Increasing physical activity with mobile devices: a meta-analysis. J
Med Internet Res. 2012; 14(6):e161. doi: 10.2196/jmir.2171 PMID: 23171838
16.
Case MA, Burwick HA, Volpp KG, Patel MS. Accuracy of smartphone applications and wearable
devices for tracking physical activity data. JAMA. 2015; 313(6):625–6. doi: 10.1001/jama.2014.17841
PMID: 25668268
17.
Ranck J. The wearable computing market: a global analysis. Gigaom Pro. 2012.
18.
Smart wearables—Statista Dossier. Fitbit—number of active users 2012–2015. 2015. Available: http://
www.statista.com/statistics/472600/fitbit-active-users/.
19.
Troiano RP, McClain JJ, Brychta RJ, Chen KY. Evolution of accelerometer methods for physical activity
research. Br J Sports Med. 2014; 48(13):1019–23. doi: 10.1136/bjsports-2014-093546 PMID:
24782483
20.
Storm FA, Heller BW, Mazza C. Step detection and activity recognition accuracy of seven physical
activity monitors. PloS One. 2015; 10(3):e0118723. doi: 10.1371/journal.pone.0118723 PMID:
25789630
21.
Diaz KM, Krupka DJ, Chang MJ, Peacock J, Ma Y, Goldsmith J, et al. Fitbit(R): An accurate and reliable
device for wireless physical activity tracking. Int J Cardiol. 2015; 185:138–40. doi: 10.1016/j.ijcard.2015.
03.038 PMID: 25795203
22.
Nelson MB, Kaminsky LA, Dickin DC, Montoye AH. Validity of consumer-based physical activity moni-
tors for specific activity types. Med Sci Sports Exerc. 2016.
23.
Schneider M, Chau L. Validation of the Fitbit Zip for monitoring physical activity among free-living ado-
lescents. BMC Res Notes. 2016; 9(1):448. doi: 10.1186/s13104-016-2253-6 PMID: 27655477
24.
Evenson KR, Goto MM, Furberg RD. Systematic review of the validity and reliability of consumer-wear-
able activity trackers. Int J Behav Nutr Phys Act. 2015; 12(1):159.
25.
Dierker K, Smith B. Comparison between four personal activity monitors and the Actigraph GT3X+ to
measure daily steps. Med Sci Sports Exerc. 2014; 46(5):792.
26.
Dominick G, Winfree K, Pohlig R, Papas M. Physical activity assessment between consumer-and
research-grade accelerometers: a comparative study in free-living conditions. JMIR MHealth UHealth.
2016; 4(3):e110. doi: 10.2196/mhealth.6281 PMID: 27644334
27.
Sushames A, Edwards A, Thompson F, McDermott R, Gebel K. Validity and reliability of fitbit flex for
step count, moderate to vigorous physical activity and activity energy expenditure. PloS One. 2016; 11
(9):e0161224. doi: 10.1371/journal.pone.0161224 PMID: 27589592
28.
Dontje ML, de Groot M, Lengton RR, van der Schans CP, Krijnen WP. Measuring steps with the Fitbit
activity tracker: an inter-device reliability study. J Med Eng Technol. 2015; 39(5):286–90. doi: 10.3109/
03091902.2015.1050125 PMID: 26017748
29.
Abel T, Graf N, Niemann S. Gender bias in the assessment of physical activity in population studies.
Soz Praventivmed. 2001; 46(4):268–72. PMID: 11582854
30.
Marquez DX, McAuley E. Gender and acculturation influences on physical activity in Latino adults. Ann
Behav Med. 2006; 31(2):138–44. doi: 10.1207/s15324796abm3102_5 PMID: 16542128
31.
Australian Bureau of Statistics. Women’s participation in sport and physical activity. Canberra, ACT;
2006.
32.
Chu AHY, Ng SH, Koh D, Mu¨ller-Riemenschneider F. Reliability and validity of the self-and interviewer-
administered versions of the Global Physical Activity Questionnaire (GPAQ). PloS One. 2015; 10(9):
e0136944. doi: 10.1371/journal.pone.0136944 PMID: 26327457
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
12 / 13
33.
Choi L, Liu Z, Matthews CE, Buchowski MS. Validation of accelerometer wear and nonwear time classi-
fication algorithm. Med Sci Sports Exerc. 2011; 43(2):357–64. doi: 10.1249/MSS.0b013e3181ed61a3
PMID: 20581716
34.
Sasaki JE, John D, Freedson PS. Validation and comparison of ActiGraph activity monitors. J Sci Med
Sport. 2011; 14(5):411–6. doi: 10.1016/j.jsams.2011.04.003 PMID: 21616714
35.
Tudor-Locke C, Barreira TV, Schuna JMJ. Comparison of step outputs for waist and wrist accelerome-
ter attachment sites. Med Sci Sports Exerc. 2015; 47(4):839–42. doi: 10.1249/MSS.
0000000000000476 PMID: 25121517
36.
Fleiss JL, Levin B, Paik MC. The measurement of interrater agreement—Statistical methods for rates
and proportions. 1981; 2:212–236.
37.
Tudor-Locke C. Steps to better cardiovascular health: How many steps does it take to achieve good
health and how confident are we in this number? Curr Cardiovasc Risk Rep. 2010; 4(4):271–6. doi: 10.
1007/s12170-010-0109-5 PMID: 20672110
38.
Barriera TV, Tudor-Locke C, Champagne CM, Broyles ST, Johnson WD, Katzmarzyk PT. Comparison
of GT3X accelerometer and YAMAX pedometer steps/day in a free-living sample of overweight and
obese adults. J Phys Act Health. 2013; 10(2):263–70. PMID: 22821951
39.
Kooiman TJ, Dontje ML, Sprenger SR, Krijnen WP, van der Schans CP, de Groot M. Reliability and
validity of ten consumer activity trackers. BMC Sports Sci Med Rehabil. 2015; 7:24. doi: 10.1186/
s13102-015-0018-5 PMID: 26464801
40.
Rosenberger ME, Haskell WL, Albinali F, Mota S, Nawyn J, Intille S. Estimating activity and sedentary
behavior from an accelerometer on the hip or wrist. Med Sci Sports Exerc. 2013; 45(5):964. doi: 10.
1249/MSS.0b013e31827f0d9c PMID: 23247702
41.
Hildebrand M, Van Hees VT, Hansen BH, Ekelund U. Age-group comparability of raw accelerometer
output from wrist-and hip-worn monitors. Med Sci Sports Exerc. 2014; 46(9):1816–24. doi: 10.1249/
MSS.0000000000000289 PMID: 24887173
42.
Tudor-Locke C, Barreira T, Schuna J, Mire E, Chaput J-P, Fogelholm M, et al. Improving wear time
compliance with a 24-hour waist-worn accelerometer protocol in the International Study of Childhood
Obesity, Lifestyle and the Environment (ISCOLE). Int J Behav Nutr Phys Act. 2015; 12(1):11.
43.
Welk G. Physical activity assessments for health-related research. Champaign, IL: Human Kinetics;
2002.
44.
John D, Freedson P. Actigraph and actical physical activity monitors: a peek under the hood. Med Sci
Sports Exerc. 2012; 44(1 Suppl 1):S86–S9.
Comparison of Fitbit Flex and ActiGraph for steps in free-living adults
PLOS ONE | DOI:10.1371/journal.pone.0172535
February 24, 2017
13 / 13
(...TRUNCATED) | Comparison of wrist-worn Fitbit Flex and waist-worn ActiGraph for measuring steps in free-living adults.(...TRUNCATED) | 02-24-2017 | Chu, Anne H Y,Ng, Sheryl H X,Paknezhad, Mahsa,Gauterin, Alvaro,Koh, David,Brown, Michael S,Müller-Riemenschneider, Falk(...TRUNCATED) | eng |
PMC10721660 | Vol.:(0123456789)
Sports Medicine (2023) 53 (Suppl 1):S7–S14
https://doi.org/10.1007/s40279-023-01876-3
REVIEW ARTICLE
Carbohydrate Nutrition and Skill Performance in Soccer
Ian Rollo1,2 · Clyde Williams2
Accepted: 8 June 2023 / Published online: 8 July 2023
© The Author(s) 2023
Abstract
In soccer, players must perform a variety of sport-specific skills usually during or immediately after running, often at sprint
speed. The quality of the skill performed is likely influenced by the volume of work done in attacking and defending over the
duration of the match. Even the most highly skilful players succumb to the impact of fatigue both physical and mental, which
may result in underperforming skills at key moments in a match. Fitness is the platform on which skill is performed during
team sport. With the onset of fatigue, tired players find it ever more difficult to successfully perform basic skills. Therefore,
it is not surprising that teams spend a large proportion of their training time on fitness. While acknowledging the central
role of fitness in team sport, the importance of team tactics, underpinned by spatial awareness, must not be neglected. It is
well established that a high-carbohydrate diet before a match and, as a supplement during match play, helps delay the onset
of fatigue. There is some evidence that players ingesting carbohydrate can maintain sport-relevant skills for the duration
of exercise more successfully compared with when ingesting placebo or water. However, most of the assessments of sport-
specific skills have been performed in a controlled, non-contested environment. Although these methods may be judged
as not ecologically valid, they do rule out the confounding influences of competition on skill performance. The aim of this
brief review is to explore whether carbohydrate ingestion, while delaying fatigue during match play, may also help retain
sport soccer-specific skill performance.
Key Points
The successful execution of repeated skilled actions is a
fundamental requirement for soccer performance.
Soccer players experience, to different degrees, physical
and mental fatigue that have a negative impact on the
performance of specific skills.
Increasing muscle and liver glycogen stores before and
ingesting carbohydrate during competition delays the
onset of fatigue and is conducive to maintaining the
execution of soccer-specific skills.
Ingesting carbohydrate, at key times during competition,
could counter negative feelings and improve concentra-
tion, helping players maintain skill execution over the
duration of exercise.
1 Introduction
In soccer, players must perform a variety of sport-specific
skills usually during or immediately after running at vari-
ous speeds. There is an obvious link between sport-spe-
cific fitness and the players’ ability to execute the relevant
skill as and when it is appropriate, when defending and
attacking. In all sport, skill is used as an umbrella term
that includes not only physical performance of a particu-
lar skill but also the complex interaction of cognitive and
technical abilities to respond to the multitude of scenarios
that occur in every match. While technical skills can be
taught to the point of being instinctive, the cognitive skill
of being able to ‘read the game’ is one that is developed
over the sporting lifespan of successful players.
Both the skill proficiency of the player and the number
of specific technical actions reduce as a match progresses
[1, 2]. In addition, the higher the tempo of a match, the
sooner players begin to experience both physical (run,
sprint, jump) and mental (concentration, decision-making)
* Ian Rollo
[email protected]
1
Gatorade Sports Science Institute, PepsiCo Life Sciences,
Global R&D, Leicestershire, UK
2
School of Sports Exercise and Health Sciences,
Loughborough University, Loughborough, UK
S8
I. Rollo, C. Williams
effects of fatigue, which often results in a decrease in
skill performance [3, 4]. This is often to the frustration of
coaches as well as spectators, who, for example, observe
a misplaced shot, an ill-timed pass or a poor decision just
when the team need it least. Therefore, teams dedicate
a large proportion of their training time to fitness [5, 6].
Fatigue during prolonged exercise is closely associated
with the depletion of the carbohydrate store (glycogen) in
skeletal muscles (for full review see Ref. [7]). In a recent
study of fatigue in a football match, Mohr et al. reported
critically low glycogen levels in the skeletal muscles
after 90 min of play and a further significant reduction
following 30 min of extra time. Players ran less and per-
formed standard skills with less accuracy than earlier in
the game [8]. An early reduction in muscle and liver gly-
cogen stores, during prolonged exercise, can be prevented
by carbohydrate ingestion before and during exercise.
Using this nutritional strategy, fatigue is delayed and per-
formance sustained for longer than in the absence of this
intervention [9]. In addition, several previous reviews have
concluded carbohydrate ingestion also facilitates the pres-
ervation of skill performance when players are fatigued
[10–12].
The aim of this paper is to discuss the most recent
studies investigating the effects of carbohydrate inges-
tion on soccer-specific skills, and the possible role that
carbohydrate ingestion plays in negating the impact that
more recently reported mental fatigue has on skill perfor-
mance. To inform this review article an electronic litera-
ture search was undertaken using three online databases
(PubMed, Web of Science, SPORTDiscus). Searches were
performed using keywords from existing relevant papers.
Search terms were ‘Soccer’, ‘Football’, ‘Carbohydrate’,
‘Skill’ and ‘Performance’ phrased as appropriate. Refer-
ence lists of all studies and relevant systematic reviews
were examined manually to identify relevant studies for
this review.
2 Skill Assessment
Skilled movements are physically complex but even more so
when performed during match play because they involve an
interaction between the physical and cognitive qualities nec-
essary to achieve successful outcomes [13]. The acquisition
of skills and their retention is a process that begins early in
the career of soccer players. By the time they become pro-
fessional players they will have achieved superior levels of
soccer-specific skills, both technical and cognitive. Further-
more, hours of team training and competitions help players
consolidate and extend the tactical execution of their skills.
Therefore, it is not surprising that the defining characteristics
of professional players are their levels of sport-specific skills
in addition to their superior physical attributes [14–16].
Traditionally, a team’s and players’ level of soccer-spe-
cific skills have been assessed by the ‘experienced eye’ of
coaches who know what is expected of professional soccer
players. The technical components of skill fall into two large
categories: closed (free kick, corners, penalties, throw-in)
and open (passing, tackling, heading, goal shooting) skills
[17].
In the modern game, skill performance is typically cap-
tured via team metrics from competitive matches, for exam-
ple, pass completion, interceptions, shots on target, chal-
lenges won and number of interceptions [18]. An important
metric is ball possession during match play. Individual play-
ers must work cohesively to create space, pass and control
the ball repeatedly whilst being challenged by the opposi-
tion. Although percentage ball possession does not guaran-
tee success, those teams with greater percentage ball pos-
session perform more passes, touches per possession, shots,
dribbles and final-third entries in comparison with teams
with low percentage ball possession [19]. On-field analyses
allow comparisons of how the speed and skill of the game
changes, from match to match and beyond. For example, an
analysis of the Men’s World Cup finals between 1966 and
2010 reported a 35% increase in the number of passes per
minute of play, which was accompanied by a 15% increase
in the speed of the match [20]. Nonetheless, while the team
metrics obtained by ever more sophisticated match analysis
technology are hugely informative, the impact of training,
rehabilitation and nutritional intervention on individual
players may be better understood by assessing their skills
by objective assessments. Desirable as this is, it is difficult
to design objective skill tests that reproduce all that goes
into the successful execution of skills in competition. As a
result, some studies have used isolated tests of soccer skill,
for example, ball juggling [21], wall volley [22], heading
[23], shooting [13, 24], passing [24–27] and dribbling [28].
Some laboratory-based studies provide controlled envi-
ronments to investigate isolated skills and also attempt to
simulate the physical demands of the sport. For example, the
Soccer Match Simulation (SMS) protocol embeds soccer-
specific skills to enhance the ecological validity of a previ-
ously validated simulated assessment of the energy demands
of a soccer match [29, 30]. However, while objective tests
of skill have many advantages, they are not without several
limitations. Rodriguez et al. discuss the importance of play-
ing surface on the ecological validity of soccer skills tests
[27, 28]. For example, dribbling a ball at speed on a smooth
floor is likely a greater challenge than executing this skill
on grass. Correspondingly, the footwear worn for differ-
ent surfaces may not be optimal for the skill under assess-
ment, such as boots versus trainers when testing shooting
skill. Furthermore, the use of sport-specific materials that
S9
Carbohydrate Nutrition and Skill Performance in Soccer
are familiar to players, such as soccer mannequins instead
of target boxes, should also be utilised [31]. Ali [17] has
described the strengths and limitations of tests of soccer
skill performance.
3 Carbohydrate Ingestion and Skill
Fitness and skill go ‘hand-in-glove’; as players tire, they are
less able to perform the relevant skills when needed [1, 2].
As mentioned earlier, there is a close association between
the development of fatigue during a match and the depletion
of players’ muscle glycogen stores, which becomes criti-
cal should the match go into extra time, extending play to
120 min [8]. Nutritional strategies to increase the body’s
glycogen stores by providing carbohydrate before and during
exercise improves endurance by delaying the depletion of
this essential fuel. The effectiveness of carbohydrate inges-
tion applies not only to constant pace running and cycling
but also to intermittent high-speed running [9], which is the
common activity pattern in team sport, especially in soccer.
How much carbohydrate should be consumed, and when, are
questions that have led to tried and tested recommendations
[5, 28, 32–37] (Table 1).
While adopting nutritional strategies to delay a rapid loss
of the body’s glycogen stores helps players maintain their
work rate during matches, the question is whether it also
helps prevent a loss of skill? A simple answer would be
that if players tire less readily, after implementing a carbo-
hydrate feeding strategy, then they would be better able to
execute the necessary skills in match play. Unfortunately,
there are too few studies to provide a definitive answer to
this question. However, one study reported that when male
professional soccer players ingested either a 7% carbo-
hydrate–electrolyte or placebo beverage before (5 ml per
kilogram body mass) and every 15 min (2 ml per kilogram
body mass) during a 90 min on-field soccer match and then
completed the assessment of four skills, dribbling speed,
coordination, precision and power, there was a significantly
improved retention of dribbling speed and precision follow-
ing carbohydrate ingestion [38].
In an innovative study on the impact of carbohydrate
ingestion on skill, tests were undertaken on players’ domi-
nant and non-dominant limbs. Using a soccer-specific pro-
tocol, higher passing scores were achieved by both dominant
and non-dominant feet following the ingestion of carbohy-
drate (30 g, before and at half time, compared with placebo
whilst drinking water ad libitum) [27]. This effect was evi-
dent from 60 min onwards. Importantly, improved perfor-
mance was attained without loss of passing speed, which
was better maintained in the non-dominant foot with carbo-
hydrate ingestion. This observation is of interest because it is
consistent with other studies in sports such as tennis, where
Table 1 Carbohydrate intake recommendations for team sport
Team sport exercise scenario Objectives
Desired adaptation/outcome
Suggested daily
carbohydrate inges-
tion range
Considerations
In-season training
(1 game per week)
To delay physical and mental fatigue
To maintain physical qualities (and improve
where possible/appropriate)
To keep players injury and illness free
To maintain aerobic and anaerobic fitness
To at least maintain strength, power, speed
To maintain lean body mass
To support physical and technical perfor-
mance
4–8 g/kg body mass Range accommodates variations in loads
across the micro-cycle (e.g. low load days
and match day − 1 carbohydrate loading
protocols) as well as individual training
goals (e.g. manipulation of body composi-
tion to accommodate weight loss and fat loss
or weight gain and lean mass gain).
Practice competition carbohydrate ingestion
regime
Match day − 1, match day
and match day + 1
6–8 g/kg body mass
to elevate muscle
glycogen stores
Ingest 1–3 g of carbohydrate per kilogram
body mass 3–4 h before a match to replenish
liver glycogen stores
Ingest 30 g of carbohydrate following the
warm-up and during the half-time interval
Ingest 1 g carbohydrate per kilogram body
mass per hour with fluids after a match to
start restoration of glycogen and rehydration
S10
I. Rollo, C. Williams
non-dominant or weaker side (backhand) shots respond posi-
tively to carbohydrate ingestion, especially when fatigued
[39]. The assessment of complex skilled actions on the non-
dominant side may require greater activation of the central
nervous system (CNS) and therefore be more susceptible to
fatigue [27]. Furthermore non-dominant skilled actions may
be more likely influenced by the arousal level of the player
[40]. Thus, the performance of players’ non-dominant sides
appears to have a greater sensitivity to carbohydrate inges-
tion [27], even though the ‘non-dominant’ side is likely to
be inferior in performing skills.
4 Carbohydrate Ingestion and Mental
Fatigue
The physiology of fatigue has been extensively studied [41].
A recent model of motor or cognitive task induced fatigue
proposes that no single factor is responsible for declines in
skill performance. Instead, fatigue is considered a psycho-
physiological condition. Motor fatigue and perceived fatigue
are interdependent but hinge on various determinants and
depend on modulating factors such as age, sex and specific
skill characteristics [42]. Mental fatigue is defined as a psy-
chobiological state that arises during prolonged demanding
cognitive activity and results in an acute feeling of tired-
ness and/or a decreased cognitive ability as well as mood
changes [43, 44]. Mental fatigue can reduce physical capac-
ity, assessed through reduced time to exhaustion and ele-
vated rating of perceived exertion (RPE) [45], and has been
shown to fluctuate throughout a competitive season [46].
To highlight this point, mental fatigue has been found, in
one review, to have a negative influence on 37% of soccer-
specific skills (n = 92) [43].
Mental fatigue has been recognised as a key considera-
tion in team sport, due to the associated negative impact
on physical, technical, decision-making and tactical perfor-
mance [47]. Contributing factors to mental fatigue in team
sport environments include but are not limited to prolonged
cognitive demands, team meetings, travel and the inability
to ‘switch off’ [48, 49].
Of note is the approach taken in laboratory studies which
use the repeated execution of inherent sport-specific skills
to induce mental fatigue [50]. Thus, tracking skill execution
may also be important because it might reflect the presence
of both mental and physical fatigue. Correspondingly, moni-
toring mental fatigue has been recommended in team sport
to provide an overall picture of how players are coping with
the demands of training and competition [51]. Therefore,
strategies are used to help avoid mental fatigue, for example,
displacement activities, such as changes in training routines,
environment and, of course, adequate rest and recovery.
Increasing dietary carbohydrate while improving exercise
capacity both in training and in competition may also be a
mood-changing countermeasure to mental fatigue [52, 53].
If players are feeling good rather than bad (pleasure–dis-
pleasure) and energized (i.e. in an activated state) before
and during matches, then it is more likely that they will per-
form better [40, 54]. For example, Backhouse et al. have
shown that the ingestion of carbohydrate elevated perceived
activation during the final 30 min of 120-min of intermit-
tent running exercise [55] and also attenuated the decline in
pleasure–displeasure during a 120-min bout of cycling [56].
Administering both a Feeling Scale (FS) and an RPE scale
allows a measure of not only ‘what’ (RPE) but also ‘how’
(FS) a person feels [57] but is rarely administered during
skill intervention studies or applied settings.
A recent review identified mouth rinsing and expectorat-
ing a carbohydrate beverage as a potential acute counter-
measure to mental fatigue [58]. The recognition of carbo-
hydrate in the mouth, when administered immediately after
a mentally fatiguing task, was linked to increased excitabil-
ity of corticomotor pathways [59, 60]. Furthermore, there
appears to be a direct link between improvements in task-
specific activity and activation within the primary senso-
rimotor cortex in response to oral carbohydrate signalling
[61]. These results contribute to a possible explanation for
improved high-intensity intermittent running performance
in response to mouth rinsing with a 10% carbohydrate bev-
erage [62, 63]. Although not all studies report this effect
[64], central activation mediated by the ingestion of carbo-
hydrate may contribute to the better retention of sprint and
technical performance observed early in exercise or in the
absence of hypoglycaemia [27, 28, 65]. While mouth rins-
ing with a carbohydrate beverage has been shown to benefit
complex whole-body skilled actions in fencers, compared
with taste-matched placebos [66], the impact on soccer skill
performance is yet to be investigated. Furthermore, it is also
important to note that mouth rinsing with non-sweet car-
bohydrate activates the reward centres of the brain and so
may contribute to the ‘feel good’ sensation that may counter
mental fatigue [67]. Nevertheless, these findings should be
considered as an additional benefit to carbohydrate inges-
tion, during or after exercise, when substrate delivery and
replenishment of glycogen stores are the respective priorities
[68–70].
These responses to carbohydrate ingestion may not be sur-
prising bearing in mind that glucose is the main fuel for the
brain and CNS [71]. For optimum functioning of the brain
and CNS, glucose homeostasis must be maintained even dur-
ing a wide range of conditions. Should blood glucose fall to
hypoglycaemic levels, then the neural drive to skeletal mus-
cles will be compromised; however, it is restored following
the ingestion of carbohydrate [72]. During exercise, the rate
of glucose release from the liver into the blood increases to
match the glucose uptake by contracting muscle [73]. In most
S11
Carbohydrate Nutrition and Skill Performance in Soccer
team sport, blood glucose concentrations are well maintained
over the duration of competition (80–90 min) and extra time
(120 min in soccer) in well-fed individuals [74]. Nevertheless,
carbohydrate ingestion at the onset of exercise is an effec-
tive strategy not only to top up muscle glycogen stores but
also because it temporarily inhibits hepatic glucose release
in a dose-dependent manner, and so conserves liver glycogen
stores [75, 76]. Carbohydrate ingestion, as a means of pre-
serving the finite store of liver glycogen, will maintain blood
glucose concentrations and performance late in exercise. This
strategy is particularly beneficial when matches extend to
extra time [8, 77]. Of interest is the observation that elevated
blood glucose concentrations are associated with improved
skill performance in comparison with euglycaemia [27, 28,
65, 78]. An immediate explanation for this observation is not
apparent other than that glucose is a fuel for the brain [79, 80].
However, the brain is sensitive to changes in blood glucose,
and the rate of change may act to monitor the availability of
whole-body carbohydrate stores.
5 Conclusion
Participants in team sport experience, to different degrees,
physical and mental fatigue that have a negative impact on
the performance of sport-specific skills. The complex series
of events between brain and skeletal muscle that interact to
minimise the impact of physical and mental fatigue on the
performance of skills during competition, following carbo-
hydrate feeding, is summarised in Fig. 1. Nutritional strate-
gies that increase muscle and liver glycogen stores prior to
competition and provide carbohydrate during competition
maintain work rate by delaying the onset of fatigue. This
effect of carbohydrate ingestion is, in itself, conducive to
maintaining the execution of sport-specific skill. Further-
more, ingesting carbohydrate, at key times during competi-
tion, could counter negative feelings and improve concentra-
tion, thereby helping players maintain skill execution over
the duration of exercise.
Acknowledgements This supplement is supported by the Gatorade
Sports Science Institute (GSSI). The supplement was guest edited
by Lawrence L. Spriet, who convened a virtual meeting of the GSSI
Expert Panel in October 2022 and received honoraria from the GSSI, a
division of PepsiCo, Inc., for his participation in the meeting. Dr Spriet
received no honoraria for guest editing this supplement. Dr Spriet
Fig. 1 Translating thoughts into skilled actions. The electro-chemical
chain of events between the brain and skeletal muscles, and how car-
bohydrate ingestion may impact skill performance. BM body mass,
SR sarcoplasmic reticulum, Ca2+ calcium, Na+/K+ sodium–potassium
pump, ATP adenosine triphosphate. ‘+’ = positive influence upon,
‘−’ = negative influence upon. Mood, motivation, RPE [52, 55, 58],
facilitation of corticomotor outputs [60, 61], blood glucose availabil-
ity, hepatic glycogen preservation [75, 76, 81, 82], muscle innerva-
tion: SR calcium handling [83], ATP generation [83–85]
S12
I. Rollo, C. Williams
suggested peer reviewers for each paper, which were sent to the Sports
Medicine Editor-in-Chief for approval, prior to any reviewers being
approached. Dr Spriet provided comments on each paper and made an
editorial decision based on comments from the peer reviewers and the
Editor-in-Chief. Where decisions were uncertain, Dr Spriet consulted
with the Editor-in-Chief. The views expressed in this manuscript are
those of the authors and do not necessarily reflect the position or policy
of PepsiCo, Inc. The authors would like to acknowledge and thank all
previous and existing colleagues and collaborators.
Declarations
Funding This article is based on a presentation by Ian Rollo to the
GSSI Expert Panel in October 2022. No honorarium for participation
in or preparation of the article for that meeting was provided by the
GSSI. No other sources of funding were utilized by the authors in the
preparation of the article for this supplement.
Conflict of interest Ian Rollo is an employee of the Gatorade Sports
Science Institute. However, the views expressed in this manuscript
are those of the authors and do not necessarily reflect the position or
policy of PepsiCo, Inc. Clyde Williams declares no conflicts of inter-
est relevant to the content of this review. While this author previously
presented to the GSSI Expert Panel in 2015, and funding for participa-
tion in that meeting together with an honorarium were provided by the
GSSI, the honorarium was donated to charity.
Author contributions IR conceived the idea for this review. IR and CW
conducted the literature search and selected the articles for inclusion in
the review. IR and CW co-wrote the first draft and revised the original
manuscript. Both authors read and approved the final version.
Open Access This article is licensed under a Creative Commons Attri-
bution 4.0 International License, which permits use, sharing, adapta-
tion, distribution and reproduction in any medium or format, as long
as you give appropriate credit to the original author(s) and the source,
provide a link to the Creative Commons licence, and indicate if changes
were made. The images or other third party material in this article are
included in the article's Creative Commons licence, unless indicated
otherwise in a credit line to the material. If material is not included in
the article's Creative Commons licence and your intended use is not
permitted by statutory regulation or exceeds the permitted use, you will
need to obtain permission directly from the copyright holder. To view a
copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.
References
1. Harper LD, West DJ, Stevenson E, Russell M. Technical perfor-
mance reduces during the extra-time period of professional soccer
match-play. PLoS ONE. 2014;9(10): e110995.
2. Rampinini E, Impellizzeri FM, Castagna C, Coutts AJ, Wisloff U.
Technical performance during soccer matches of the Italian Serie
A league: effect of fatigue and competitive level. J Sci Med Sport.
2009;12(1):227–33.
3. Mohr M, Krustrup P, Bangsbo J. Fatigue in soccer: a brief review.
J Sports Sci. 2005;23(6):593–9.
4. Smith MR, Zeuwts L, Lenoir M, Hens N, De Jong LM, Coutts
AJ. Mental fatigue impairs soccer-specific decision-making skill.
J Sports Sci. 2016;34(14):1297–304.
5. Anderson L, Orme P, Di Michele R, Close GL, Morgans R,
Drust B, Morton JP. Quantification of training load during one-,
two- and three-game week schedules in professional soccer
players from the English Premier League: implications for car-
bohydrate periodisation. J Sports Sci. 2016;34(13):1250–9.
6. Papadakis L, Tymvios C, Patras K. The relationship between
training load and fitness indices over a pre-season in professional
soccer players. J Sports Med Phys Fit. 2020;60(3):329–37.
7. Mohr M, Vigh-Larsen JF, Krustrup P. Muscle glycogen in Elite
Soccer—a perspective on the implication for performance,
fatigue, and recovery. Front Sports Active Living. 2022;4:
876534.
8. Mohr M, Ermidis G, Jamustas AZ, Vigh-Larsen J, Poulios A,
Draganidis D, Papanikolaou K, Tsimeas P, Batsilas D, Loules
G, Batrakoulis A, Sovatzidis A, Nielsen JL, Tzatzakis T, Deli
CK, Nybo L, Krustrup P, Fatouros IG. Extended match time
exacerbates fatigue and impacts physiological responses in male
soccer players. Med Sci Sports Exerc. 2022;55(1):80–92.
9. Williams C, Rollo I. Carbohydrate nutrition and team sport per-
formance. Sports Med. 2015;45(Suppl 1):S13-22.
10. Hills SP, Russell M. Carbohydrates for soccer: a focus on skilled
actions and half-time practices. Nutrients. 2017;10(1):22–32.
11. Baker LB, Rollo I, Stein KW, Jeukendrup AE. Acute effects
of carbohydrate supplementation on intermittent sports perfor-
mance. Nutrients. 2015;7(7):5733–63.
12. Russell M, Kingsley M. The efficacy of acute nutritional
interventions on soccer skill performance. Sports Med.
2014;44(7):957–70.
13. Haaland E, Hoff J. Non-dominant leg training improves the
bilateral motor performance of soccer players. Scand J Med
Sci Sports. 2003;13(3):179–84.
14. Slimani M, Nikolaidis PT. Anthropometric and physiological
characteristics of male soccer players according to their competi-
tive level, playing position and age group: a systematic review. J
Sports Med Phys Fit. 2019;59(1):141–63.
15. Cometti G, Maffiuletti NA, Pousson M, Chatard JC, Maffulli N.
Isokinetic strength and anaerobic power of elite, subelite and ama-
teur French soccer players. Int J Sports Med. 2001;22(1):45–51.
16. Gouveia JN, França C, Martins F, Henriques R, Nascimento
MM, Ihle A, Sarmento H, Przednowek K, Martinho D, Gouveia
ÉR. Characterization of static strength, vertical jumping, and
isokinetic strength in soccer players according to age, competi-
tive level, and field position. Int J Environ Res Public Health.
2023;20(3):1799. https:// doi. org/ 10. 3390/ ijerp h2003 1799
17. Ali A. Measuring soccer skill performance: a review. Scand J Med
Sci Sports. 2011;21(2):170–83.
18. Andrzejewski M, Oliva-Lozano JM, Chmura P, Chmura J,
Czarniecki S, Kowalczuk E, Rokita A, Muyor JM, Konefal M.
Analysis of team success based on match technical and running
performance in a professional soccer league. BMC Sports Sci Med
Rehabil. 2022;14(1):82.
19. Bradley PS, Lago-Penas C, Rey E, Gomez Diaz A. The effect of
high and low percentage ball possession on physical and technical
profiles in English FA Premier League soccer matches. J Sports
Sci. 2013;31(12):1261–70.
20. Wallace JL, Norton KI. Evolution of World Cup soccer final
games 1966–2010: game structure, speed and play patterns. J Sci
Med Sport. 2014;17(2):223–8.
21. Hoare DG, Warr CR. Talent identification and women’s soccer:
an Australian experience. J Sports Sci. 2000;18(9):751–8.
22. Vanderford ML, Meyers MC, Skelly WA, Stewart CC, Hamilton
KL. Physiological and sport-specific skill response of Olympic
youth soccer athletes. J Strength Cond Res. 2004;18(2):334–42.
23. Rosch D, Hodgson R, Peterson TL, Graf-Baumann T, Junge A,
Chomiak J, Dvorak J. Assessment and evaluation of football per-
formance. Am J Sports Med. 2000;28(5 Suppl):S29-39.
24. Ali A, Williams C. Carbohydrate ingestion and soccer skill per-
formance during prolonged intermittent exercise. J Sports Sci.
2009;27(14):1499–508.
S13
Carbohydrate Nutrition and Skill Performance in Soccer
25. Rostgaard T, Iaia FM, Simonsen DS, Bangsbo J. A test to evaluate
the physical impact on technical performance in soccer. J Strength
Cond Res. 2008;22(1):283–92.
26. Bendiksen M, Bischoff R, Randers MB, Mohr M, Rollo I, Suetta
C, Bangsbo J, Krustrup P. The Copenhagen Soccer Test: physi-
ological response and fatigue development. Med Sci Sports Exerc.
2012;44(8):1595–603.
27. Rodriguez-Giustiniani P, Rollo I, Witard OC, Galloway SDR.
Ingesting a 12% carbohydrate-electrolyte beverage before
each half of a soccer match simulation facilitates retention
of passing performance and improves high-intensity running
capacity in academy players. Int J Sport Nutr Exerc Metab.
2019;29(4):397–405.
28. Harper LD, Stevenson EJ, Rollo I, Russell M. The influence of
a 12% carbohydrate-electrolyte beverage on self-paced soccer-
specific exercise performance. J Sci Med Sport. 2017;12:1123–9.
29. Russell M, Rees G, Benton D, Kingsley M. An exercise pro-
tocol that replicates soccer match-play. Int J Sports Med.
2011;32(7):511–8.
30. Nicholas CW, Nuttall FE, Williams C. The Loughborough Inter-
mittent Shuttle Test: a field test that simulates the activity pattern
of soccer. J Sports Sci. 2000;18(2):97–104.
31. Rodriguez-Giustiniani P, Rollo I, Galloway SDR. A preliminary
study of the reliability of soccer skill tests within a modified soc-
cer match simulation protocol. Sci Med Footb. 2021;6(3):363–71.
32. Collins J, Maughan RJ, Gleeson M, Bilsborough J, Jeukendrup
A, Morton JP, Phillips SM, Armstrong L, Burke LM, Close GL,
Duffield R, Larson-Meyer E, Louis J, Medina D, Meyer F, Rollo
I, Sundgot-Borgen J, Wall BT, Boullosa B, Dupont G, Lizarraga
A, Res P, Bizzini M, Castagna C, Cowie CM, D’Hooghe M,
Geyer H, Meyer T, Papadimitriou N, Vouillamoz M, McCall A.
UEFA expert group statement on nutrition in elite football current
evidence to inform practical recommendations and guide future
research. Br J Sports Med. 2021;55(8):416.
33. Thomas DT, Erdman KA, Burke LM. Position of the Academy of
Nutrition and Dietetics, Dietitians of Canada, and the American
College of Sports Medicine: nutrition and athletic performance. J
Acad Nutr Diet. 2016;116(3):501–28.
34. Rollo I, Randell RK, Baker L, Leyes JY, Medina Leal D, Lizarraga
A, Mesalles J, Jeukendrup AE, James LJ, Carter JM. Fluid bal-
ance, sweat Na+ losses, and carbohydrate intake of elite male
soccer players in response to low and high training intensities in
cool and hot environments. Nutrients. 2021;13(2):401. https:// doi.
org/ 10. 3390/ nu130 20401
35. Moss SL, Randell RK, Burgess D, Ridley S, ÓCairealláin C, Alli-
son R, Rollo I. Assessment of energy availability and associated
risk factors in professional female soccer players. Eur J Sport Sci.
2020;6:861–70.
36. Funnell MP, Dykes NR, Owen EJ, Mears SA, Rollo I, James LJ.
Ecologically valid carbohydrate intake during soccer-specific
exercise does not affect running performance in a fed state. Nutri-
ents. 2017;9(1):39. https:// doi. org/ 10. 3390/ nu901 0039
37. Burke LM, Hawley JA, Wong SH, Jeukendrup AE. Carbohy-
drates for training and competition. J Sports Sci. 2011;29(Suppl
1):S17-27.
38. Ostojic SM, Mazic S. Effects of a carbohydrate-electrolyte drink
on specific soccer tests and performance. J Sports Sci Med.
2002;1(2):47–53.
39. McRae KA, Galloway SD. Carbohydrate-electrolyte drink inges-
tion and skill performance during and after 2 hr of indoor tennis
match play. Int J Sport Nutr Exerc Metab. 2012;22(1):38–46.
40. McMorris T, Graydon J. The effect of exercise on cogni-
tive performance in soccer-specific tests. J Sports Sci.
1997;15(5):459–68.
41. Enoka RM, Baudry S, Rudroff T, Farina D, Klass M, Duchateau J.
Unraveling the neurophysiology of muscle fatigue. J Electromyogr
Kinesiol. 2011;21(2):208–19.
42. Behrens M, Gube M, Chaabene H, Prieske O, Zenon A, Broscheid
KC, Schega L, Husmann F, Weippert M. Fatigue and human per-
formance: an updated framework. Sports Med. 2023;53(1):7–31.
https:// doi. org/ 10. 1007/ s40279- 022- 01748-2
43. Habay J, Van Cutsem J, Verschueren J, De Bock S, Proost M, De
Wachter J, Tassignon B, Meeusen R, Roelands B. Mental fatigue
and sport-specific psychomotor performance: a systematic review.
Sports Med. 2021;51(7):1527–48.
44. Roelands B, Kelly V, Russell S, Habay J. The physiological nature
of mental fatigue: current knowledge and future avenues for sport
science. Int J Sports Physiol Perform. 2022;17(2):149–50.
45. Marcora SM, Staiano W, Manning V. Mental fatigue impairs
physical performance in humans. J Appl Physiol (1985).
2009;106(3):857–64.
46. Russell S, Jenkins DG, Halson SL, Juliff LE, Kelly VG. How do
elite female team sport athletes experience mental fatigue? Com-
parison between international competition, training and prepara-
tion camps. Eur J Sport Sci. 2022;22(6):877–87.
47. Smith MR, Thompson C, Marcora SM, Skorski S, Meyer T,
Coutts AJ. Mental fatigue and soccer: current knowledge and
future directions. Sports Med. 2018;48(7):1525–32.
48. Thompson CJ, Noon M, Towlson C, Perry J, Coutts AJ, Harper
LD, Skorski S, Smith MR, Barrett S, Meyer T. Understanding the
presence of mental fatigue in English academy soccer players. J
Sports Sci. 2020;38(13):1524–30.
49. Thompson CJ, Smith A, Coutts AJ, Skorski S, Datson N, Smith
MR, Meyer T. Understanding the presence of mental fatigue in
elite female football. Res Q Exerc Sport. 2022;93(3):504–15.
50. Bian C, Ali A, Nassis GP, Li Y. Repeated interval Loughborough
soccer passing tests: an ecologically valid motor task to induce
mental fatigue in soccer. Front Physiol. 2021;12: 803528.
51. Thompson CJ, Fransen J, Skorski S, Smith MR, Meyer T, Bar-
rett S, Coutts AJ. Mental fatigue in football: is it time to shift the
goalposts? An evaluation of the current methodology. Sports Med.
2019;49(2):177–83.
52. Achten J, Halson SL, Moseley L, Rayson MP, Casey A, Jeuken-
drup AE. Higher dietary carbohydrate content during intensified
running training results in better maintenance of performance and
mood state. J Appl Physiol. 2004;96(4):1331–40.
53. Killer SC, Svendsen IS, Jeukendrup AE, Gleeson M. Evidence
of disturbed sleep and mood state in well-trained athletes during
short-term intensified training with and without a high carbohy-
drate nutritional intervention. J Sports Sci. 2017;35(14):1402–10.
54. Acevedo E, Gill D, Goldfarb A, Boyer B. Affect and per-
ceived exertion during a two-hour run. Int J Sport Psychol.
1996;27:286–92.
55. Backhouse SH, Ali A, Biddle SJ, Williams C. Carbohydrate
ingestion during prolonged high-intensity intermittent exercise:
impact on affect and perceived exertion. Scand J Med Sci Sports.
2007;17(5):605–10.
56. Backhouse SH, Bishop NC, Biddle SJ, Williams C. Effect of car-
bohydrate and prolonged exercise on affect and perceived exer-
tion. Med Sci Sports Exerc. 2005;37(10):1768–73.
57. Hardy CJ, Rejeski W. Not what, but how ones feels: the meas-
urement of affect during exercise. J Sport Exerc Psychol.
1989;11:304–17.
58. Proost M, Habay J, De Wachter J, De Pauw K, Rattray B, Meeusen
R, Roelands B, Van Cutsem J. How to tackle mental fatigue: a sys-
tematic review of potential countermeasures and their underlying
mechanisms. Sports Med. 2022;52(9):2129–58.
59. Bailey SP, Harris GK, Lewis K, Llewellyn TA, Watkins R, Weaver
MA, Roelands B, Van Cutsem J, Folger SF. Impact of a carbohy-
drate mouth rinse on corticomotor excitability after mental fatigue
S14
I. Rollo, C. Williams
in healthy college-aged subjects. Brain Sci. 2021;11(8):972.
https:// doi. org/ 10. 3390/ brain sci11 080972
60. Gant N, Stinear CM, Byblow WD. Carbohydrate in the
mouth immediately facilitates motor output. Brain Res.
2010;1350:151–8.
61. Turner CE, Byblow WD, Stinear CM, Gant N. Carbohydrate in
the mouth enhances activation of brain circuitry involved in motor
performance and sensory perception. Appetite. 2014;80:212–9.
62. Rollo I, Homewood G, Williams C, Carter J, Goosey-Tolfrey
VL. The influence of carbohydrate mouth rinse on self-selected
intermittent running performance. Int J Sport Nutr Exerc Metab.
2015;25(6):550–8.
63. Kasper AM, Cocking S, Cockayne M, Barnard M, Tench J, Parker
L, McAndrew J, Langan-Evans C, Close GL, Morton JP. Carbo-
hydrate mouth rinse and caffeine improves high-intensity interval
running capacity when carbohydrate restricted. Eur J Sport Sci.
2016;16(5):560–8.
64. Gough LA, Faghy M, Clarke N, Kelly AL, Cole M, Lun Foo W.
No independent or synergistic effects of carbohydrate-caffeine
mouth rinse on repeated sprint performance during simulated
soccer match play in male recreational soccer players. Sci Med
Footb. 2022;6(4):519–27.
65. Ali A, Williams C, Nicholas CW, Foskett A. The influence of
carbohydrate-electrolyte ingestion on soccer skill performance.
Med Sci Sports Exerc. 2007;39(11):1969–76.
66. Rowlatt G, Bottoms L, Edmonds CJ, Buscombe R. The effect of
carbohydrate mouth rinsing on fencing performance and cogni-
tive function following fatigue-inducing fencing. Eur J Sport Sci.
2017;17(4):433–40.
67. Chambers ES, Bridge MW, Jones DA. Carbohydrate sensing in the
human mouth: effects on exercise performance and brain activity.
J Physiol. 2009;587(Pt 8):1779–94.
68. Rollo I, Gonzalez JT, Fuchs CJ, van Loon LJC, Williams C. Pri-
mary, secondary, and tertiary effects of carbohydrate ingestion
during exercise. Sports Med. 2020;50(11):1863–71.
69. Erith S, Williams C, Stevenson E, Chamberlain S, Crews P,
Rushbury I. The effect of high carbohydrate meals with different
glycemic indices on recovery of performance during prolonged
intermittent high-intensity shuttle running. Int J Sport Nutr Exerc
Metab. 2006;16(4):393–404.
70. Rollo I, Williams C, Nevill M. Influence of ingesting versus mouth
rinsing a carbohydrate solution during a 1-h run. Med Sci Sports
Exerc. 2011;43(3):468–75.
71. Mergenthaler P, Lindauer U, Dienel GA, Meisel A. Sugar for the
brain: the role of glucose in physiological and pathological brain
function. Trends Neurosci. 2013;36(10):587–97.
72. Nybo L. CNS fatigue and prolonged exercise: effect of glucose
supplementation. Med Sci Sports Exerc. 2003;35(4):589–94.
73. Wasserman DH. Four grams of glucose. Am J Physiol-Endocrinol
Metab. 2009;296(1):E11-21.
74. Harper LD, Briggs MA, McNamee G, West DJ, Kilduff LP,
Stevenson E, Russell M. Physiological and performance effects
of carbohydrate gels consumed prior to the extra-time period
of prolonged simulated soccer match-play. J Sci Med Sport.
2016;19(6):509–14.
75. Jeukendrup AE, Wagenmakers AJ, Stegen JH, Gijsen AP, Brouns
F, Saris WH. Carbohydrate ingestion can completely suppress
endogenous glucose production during exercise. Am J Physiol.
1999;276(4 Pt 1):E672–83.
76. Newell ML, Wallis GA, Hunter AM, Tipton KD, Galloway SDR.
Metabolic responses to carbohydrate ingestion during exercise:
associations between carbohydrate dose and endurance perfor-
mance. Nutrients. 2018;10(1):37. https:// doi. org/ 10. 3390/ nu100
10037
77. Field A, Naughton RJ, Haines M, Lui S, Corr LD, Russell M, Page
RM, Harper LD. The demands of the extra-time period of soccer:
a systematic review. J Sport Health Sci. 2022;11(3):403–14.
78. Ali A, Williams C. Carbohydrate ingestion and soccer skill per-
formance during prolonged intermittent exercise. J Sports Sci.
2009;27(14):1499–508. https:// doi. org/ 10. 1080/ 02640 41090
33347 72
79. Lopez-Gambero AJ, Martinez F, Salazar K, Cifuentes M, Nualart
F. Brain glucose-sensing mechanism and energy homeostasis. Mol
Neurobiol. 2019;56(2):769–96.
80. van Praag H, Fleshner M, Schwartz MW, Mattson MP. Exercise,
energy intake, glucose homeostasis, and the brain. J Neurosci.
2014;34(46):15139–49.
81. Gonzalez JT, Fuchs CJ, Betts JA, van Loon LJ. Liver glycogen
metabolism during and after prolonged endurance-type exercise.
Am J Physiol-Endocrinol Metab. 2016;311(3):E543–53.
82. Fuchs CJ, Gonzalez JT, Beelen M, Cermak NM, Smith FE,
Thelwall PE, Taylor R, Trenell MI, Stevenson EJ, van Loon LJ.
Sucrose ingestion after exhaustive exercise accelerates liver, but
not muscle glycogen repletion compared with glucose ingestion
in trained athletes. J Appl Physiol (1985). 2016;120(11):1328–34.
83. Ortenblad N, Nielsen J, Saltin B, Holmberg HC. Role of glyco-
gen availability in sarcoplasmic reticulum Ca2+ kinetics in human
skeletal muscle. J Physiol. 2011;589(Pt 3):711–25.
84. Duhamel TA, Stewart RD, Tupling AR, Ouyang J, Green HJ. Mus-
cle sarcoplasmic reticulum calcium regulation in humans during
consecutive days of exercise and recovery. J Appl Physiol (1985).
2007;103(4):1212–20.
85. Nielsen J, Holmberg HC, Schroder HD, Saltin B, Ortenblad N.
Human skeletal muscle glycogen utilization in exhaustive exer-
cise: role of subcellular localization and fibre type. J Physiol.
2011;589(Pt 11):2871–85.
(...TRUNCATED) | Carbohydrate Nutrition and Skill Performance in Soccer.(...TRUNCATED) | 07-08-2023 | Rollo, Ian,Williams, Clyde(...TRUNCATED) | eng |
PMC8171865 | RESEARCH ARTICLE
Effects of a period without mandatory
physical training on maximum oxygen uptake
and anthropometric parameters in naval
cadets
A´ lvaro Huerta OjedaID*☯, Guillermo Barahona-FuentesID☯, Sergio Galdames Maliqueo☯
Grupo de Investigacio´n en Salud, Actividad Fı´sica y Deporte ISAFYD, Escuela de Educacio´n Fı´sica,
Universidad de Las Ame´ricas, sede Viña del Mar, Chile
☯ These authors contributed equally to this work.
* [email protected]
Abstract
The effects of a period without physical training on the civilian population are well estab-
lished. However, no studies show the effects of a period without mandatory physical training
on maximum oxygen uptake (VO2 max) and anthropometric parameters in naval cadets.
This study aimed to investigate changes in VO2 max and anthropometric parameters after
12 weeks without mandatory physical training in naval cadets. The sample was 38 healthy
and physically active naval cadets. The measured variables, including VO2 max and anthro-
pometric parameters, were evaluated through the 12-minute race test (12MRT) and the
somatotype. Both variables had a separation of 12 weeks without mandatory physical train-
ing. A t-test for related samples was used to evidence changes between the test and post-
test; effect size was calculated through Cohen’s d-test. Distance in 12MRT and VO2 max
showed significant decreases at the end of 12 weeks without mandatory physical training (p
< 0.001). Likewise, the tricipital skinfold thickness and the endomorphic component showed
significant increases (p < 0.05). 12 weeks without mandatory physical training significantly
reduces the VO2 max in naval cadets. Simultaneously, the same period without physical
training increases both the tricipital skinfold thickness and the endomorphic component in
this population.
Introduction
Increased physical capabilities through strength training [1, 2] and aerobic capacity [3] have
been associated with health, quality of life, and sports performance benefits [1–3]. In this
sense, people included in strength training have shown neuronal and morphological adapta-
tions [4]; these two adaptations, generated by strength training, allow for the improvement of
both the metabolic health [5] and the quality of life of people [6]. At the same time, aerobic
training has reported significant decreases in cardiovascular risk factors [7], as well as an
increase in maximum oxygen uptake (VO2 max) [3]. Specifically, the VO2 max has a direct
PLOS ONE
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
1 / 15
a1111111111
a1111111111
a1111111111
a1111111111
a1111111111
OPEN ACCESS
Citation: Huerta Ojeda A´, Barahona-Fuentes G,
Galdames Maliqueo S (2021) Effects of a period
without mandatory physical training on maximum
oxygen uptake and anthropometric parameters in
naval cadets. PLoS ONE 16(6): e0251516. https://
doi.org/10.1371/journal.pone.0251516
Editor: Randy Wayne Bryner, West Virginia
University, UNITED STATES
Received: October 10, 2020
Accepted: April 27, 2021
Published: June 2, 2021
Copyright: © 2021 Huerta Ojeda et al. This is an
open access article distributed under the terms of
the Creative Commons Attribution License, which
permits unrestricted use, distribution, and
reproduction in any medium, provided the original
author and source are credited.
Data Availability Statement: The data underlying
this study are publicly available at: https://doi.org/
10.6084/m9.figshare.14049590.
Funding: The author(s) received no specific
funding for this work.
Competing interests: The authors have declared
that no competing interests exist.
association with the quality of life of people [8]. These morphological and metabolic changes,
triggered by force training or aerobic training, are experienced by both the civilian population
[9] and the military and naval population [10–12]; in the latter, they provide specific physical
characteristics that allow missions to be carried out efficiently and with a low risk of injury
[13].
Scientific evidence shows that physical training acts as a physiological stressor, increasing
energy expenditure [14], anabolic hormone concentrations [15], arterial diameter, and blood
flow [16]. These responses to physical training contribute to a physiological adaptation of the
body [17], specifical adaptations of muscles [18], and bone tissues [19]. In this sense, a recently
published meta-analysis showed the benefits of eccentric strength training through isoinertial
devices; the study results showed increases in strength, power, and muscle size with this train-
ing [20]. Concerning aerobic training, these stimuli have been considered as the primary
method to improve markers of cardiorespiratory fitness, mainly VO2 max [21]. Additionally,
physical training carried out regularly, and with the principles of intensity, volume, and fre-
quency, will minimize muscular fatigue [22] and favor the physiological adaptations of the
body [17]. Despite the above, there is also a transition phase in sports periodization [23]; this
stage corresponds to the interruption of physical training [24], which can be short term (less
than four weeks) or long term (more than four weeks) [25]. However, if professionals do not
control the transition phase, there is a high probability of provoking a detraining [25]. In this
way, a period without physical training can generate a partial or total loss of morphological
adaptations, physiological adaptations, and physical performance [26], as well as cause alter-
ations in the psychological well-being of the population [27].
The sports transition phase is an opportunity for the physical recovery of athletes [23].
However, there are unplanned situations that generate periods of non-physical training in the
population [28–30], for example, the period of vacation experienced by students each year [28]
or the current period of confinement generated by COVID-19 [30]. Regardless of the reasons,
an extended time-period without physical training has been shown to negatively influence ath-
letes’ body composition [23], increasing fat mass and decreasing lean mass [31–33]. It has also
been shown that a period without physical training of fewer than eight weeks leads to a
decrease in muscle cross-section [34], decreases in maximum strength [35], and a reduction in
VO2 max in both the civilian [36] and naval [37] populations.
Currently, naval personnel has been the subject of several research studies [38, 39]. One of
the reasons for the growing number of investigations in this sample is that the Chilean Navy
comprises more than 25,000 personnel. Of this number, 9.6% (equivalent to 2,400 personnel)
corresponds to naval officers, all trained at the Arturo Prat Naval Academy [40]. These figures
show several aspects, such as the high number of officers [40] and, therefore, the need for this
population to be studied from a psychological [11, 13], health [12] and physical [10, 38] perfor-
mance perspective. This last dimension includes the transition phase considering that we
hypothesize that naval cadets decrease their physical condition, associated with VO2 max and
anthropometric parameters, after a period without mandatory physical training; thus, with
correctly applied training loads, physical fitness loss in this phase could be avoided [23–25].
Despite the existence of studies showing a decrease in the physical condition and anthropo-
metric parameters after a period without physical training in some segments of the population
[23, 31–33], the available evidence in the naval population is scarce and limited [37]. Likewise,
and as far as knowledge goes, no studies evidence the effects of periods without physical train-
ing on VO2 max and anthropometric parameters in naval cadets from 18 to 25 years old. Con-
sequently, this study aimed to evidence the changes in VO2 max and anthropometric
parameters after 12 weeks without mandatory physical training in naval cadets from 18 to 25
years old.
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
2 / 15
Materials and methods
Research design
This study was empirical research with a manipulative, quasi-experimental strategy with a lon-
gitudinal design with repeated means [41]. To highlight the changes in VO2 max and anthro-
pometric parameters, the 12-minute race test (12MRT) and the somatotype were evaluated 12
weeks apart, a period without mandatory physical training (Fig 1).
Procedures
As a first action, all participants who voluntarily accepted to be part of the study (non-probabi-
listic sample) were recruited. The purpose and procedures of the study were indicated in an
informative talk. The inclusion criteria were that all participants should be healthy, physically
active [21] and between 18 and 25 years of age, while the exclusion criteria were: prevalence of
musculoskeletal injuries, pre-existing cardiac pathologies, abnormal respiratory and cardiac
responses during the familiarization period and inability to perform the 12MRT. All partici-
pants were asked not to engage in physical training that would generate nervous or musculo-
skeletal fatigue 48 hours before the measurements and refrain from ingesting caffeine or any
substance that could increase their metabolism during the assessment. Finally, only those par-
ticipants who signed informed consent were subjected to 12MRT and somatotype evaluations.
Participants
Thirty-eight healthy and physically active naval cadets volunteered to participate in this study
(Table 1). The type of sampling was non-probabilistic for convenience. All participants were
informed of the study objective and possible risks of the experiment. Indeed, all participants
signed the informed consent form before the implementation of the protocols. The informed
consent and the study were approved by the Human Research Committee of the University of
Las Americas (registry number CEC-FP-2020011). The informed consent and the study were
conducted under the Declaration of Helsinki (WMA 2000, Bosˇnjak 2001, Tyebkhan 2003),
which sets out the fundamental ethical principles for research with human subjects.
Fig 1. Research design. 12MRT: 12-minute race test.
https://doi.org/10.1371/journal.pone.0251516.g001
Table 1. Characterization of the participants.
Women (n = 8)
Men (n = 30)
All (n = 38)
mean ± SD (min–max)
Mean ± SD (min–max)
mean ± SD (min–max)
Age (years)
21.0 ± 1.51 (19–23)
20.5 ± 1.22 (18–24)
20.6 ± 1.28 (18–24)
BMI (kg/m2)
21.9 ± 1.79 (20.2–25.5)
22.7 ± 1.69 (20.4–26.7)
22.5 ± 1.72 (20.2–26.7)
% Fat
23.3 ± 4.7 (18.5–33.1)
12.6 ± 2.2 (9.3–18.1)
14.9 ± 5.2 (9.3–33.1)
VO2 max (mLO2kg–1min–1)
46.7 ± 3.9 (42.6–51.5)
59.3 ± 4.7 (50.9–65.5)
56.6 ± 6.9 (42.6–65.5)
SD: standard deviation; kg/m2: kilograms per square meters; min: minimum; max: maximum; %: percentage; VO2 max: maximum oxygen uptake; mLO2kg–1min–1:
milliliters of oxygen per kilogram of body mass per minute.
https://doi.org/10.1371/journal.pone.0251516.t001
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
3 / 15
Somatotype evaluation
The somatotype corresponds to the shape of the human body. It is obtained by analyzing the
arm and leg’s circumferences, the humerus and femur’s diameters, four skinfolds (tricipital,
subscapular, supra-iliac, and mid-calf), and the weight and height of a person. Body shape can
be represented two-dimensionally through the somatochart or three-dimensionally through
the compogram; the latter representation corresponds to three numerical values representing
the endomorphic, mesomorphic, and ectomorphic components of a participant (always in that
order) [42]. To represent a participant’s morphology, Berral [42] recommends using both the
somatochart and the compogram since using only the somatochart can generate an error in
interpreting the results; for example, values 3–5–3 and 4–6–4 would be represented with the
same point on the somatochart [42].
Body mass and height.
The method used to determine the participants’ somatotype was pro-
posed by Carter & Heath [43]. The body mass (kg) was evaluated through a Tanita Inner Scan
BC-5541 digital scale, with the participants barefoot, in shorts, and wearing a light shirt. The height
was measured through a Seca1 stadiometer from the feet to the vertex (Frankfort plane) [44].
Circumferences.
Arm and leg circumferences, humeral and femoral diameters, and skin
folds were evaluated with the FAGA SLR1 anthropometric kit. The circumference of the
right leg was evaluated in this segment’s bulkiest area, in a standing position and with the gas-
trocnemius relaxed; in contrast, the circumference of the right arm was evaluated in the bulki-
est area of the contracted biceps; this evaluation was performed standing with the elbow in
front and bent at 90 [43].
Diameters.
The humeral epicondyle distance was considered the humerus’s diameter,
which is the distance between the epicondyle and the right arm’s epitrochlea. For this evalua-
tion, participants were standing with the elbow bent at 90˚. The distance between the femoral
condyles (medial and distal) was considered the femur’s diameter, which evaluation was per-
formed in a sitting position with the right knee bent at 90˚ [43, 44].
Skinfold thickness.
Four skinfolds were considered to determine the participants’
somatotype: tricipital, subscapular, supra-iliac, and mid-calf [43–45].
Body Mass Index (BMI).
The BMI’s interpretation was made according to anthropomet-
ric standards to evaluate nutritional status [46].
Percentage of fat (%). The fat percentage was evaluated through impedance measurement
with the Tanita Inner Scan BC-5541 digital scale.
Waist-Hip Index (WHI).
The WHI was obtained by dividing the waist perimeter, mea-
sured at a point equidistant from the lower edge of the last rib and the iliac crest, by the perim-
eter of the hips, measured at the greatest prominence of the buttocks [44, 47].
12 weeks without mandatory physical training
In regular class periods, the naval cadets had an average of two hours of daily mandatory phys-
ical training (Monday through Saturday). This physical training was mandatory and consid-
ered loads with the orientation to all physical capacities (strength, power, flexibility, speed,
aerobic capacity and aerobic power). However, upon leaving school, whether for vacation or
unplanned situations such as the current COVID 19 pandemic [30], the physical training regi-
men was not mandatory. During the 12 weeks without mandatory physical training, the naval
cadets voluntarily took part in walking, cycling, and ball games, among other activities.
Standardized warm-up
For both the first and the second evaluation of the 12MRT, the warm-up consisted of 10 min-
utes of jogging, then 5 minutes of ballistic movements of the lower limb (adduction, abduction,
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
4 / 15
flexion, and extension of hips, and flexion and extension of knees and ankles). To finish, par-
ticipants performed three 80-meter accelerations. After this warm-up and before running the
12MRT, there was a 5-minute break.
12-minute race test
The evaluation of the 12MRT was carried out on a 400-meter athletic track. Before the evalua-
tion, participants were instructed to perform as much distance as possible within the test’s 12
minutes. During the application of the test, the participants received verbal incentives from
the researchers. The distance achieved in meters was converted into kilometers, and then the
VO2 max was obtained through the following equation [48]:
VO2 max ðmLO2 kgthe tricipital skinfold participants, a very large, negative correlation was observed between
both variables (r = -0.76, p = 0.01). At the end of the 12 weeks without mandatory physical
training (post-test), a very large, negative correlation was observed between VO2 max and the
participants’ tricipital skinfold (r = -0.81, p = 0.01). The graphic representation of these analy-
ses is presented in Fig 4.
Discussion
Concerning this study’s primary objective, the variables of VO2 max and anthropometric
parameters showed changes after the 12 weeks without mandatory physical training in naval
cadets from 18 to 25 years old. The findings revealed that the analysis initial point relates phys-
ical training to quality of life [6, 8] and sports performance [1–3]. In this way, detrimental
physiological changes and a decline in performance observed after a period without physical
training can be reversed by applying correct training loads and professional supervision [17].
Specifically, the present study’s findings showed a significant decrease in the VO2 max of naval
cadets, both men and women, after 12 weeks without mandatory physical training (p < 0.001,
ES = 0.34). Similarly, Liguori et al. [37] determined changes in VO2 max after a vacation period
without mandatory training; at the end of the vacation period, the researchers reported signifi-
cant decreases in relative (p = 0.009) and absolute (p = 0.001) VO2 max in both men and
women. Likewise, Sotiropoulos et al. [33] evaluated changes in VO2 max after a four-week
transition period in soccer players. The experimental group (EG) conducted a directed
Table 2. Mean values and SD before and after 12 weeks without mandatory physical training (n = 38).
Test
mean ± SD
Post test
mean ± SD
Related differences
Mean
SD
SEM
95% confidence
interval
t
p
d
Lower
Upper
Weight (kg)
67.1 ± 8.0
67.5 ± 8.3
-0.32
1.78
0.28
-0.91
0.25
-1.13
ns
0.01
BMI (kg/m2)
22.5 ± 1.7
22.7 ± 1.8
-0.16
0.58
0.09
-0.35
0.02
-1.78
ns
0.10
% Fat
14.9 ± 5.2
14.9 ± 5.4
0.05
1.24
0.2
-0.35
0.46
0.26
ns
0.01
WHI
0.84 ± 0.05
0.83 ± 0.04
0.00
0.03
0.00
0.00
0.01
0.71
ns
0.08
WHeI
0.46 ± 0.03
0.46 ± 0.02
0.00
0.01
0.00
0.00
0.00
0.84
ns
0.08
Tricipital skinfold (mm)
11.1 ± 3.9
11.8 ± 4.0
-0.69
1.83
0.29
-1.29
-0.09
-2.34
ns
0.18
Subscapular skinfold (mm)
10.7 ± 3.1
10.9 ± 3.0
-0.26
1.32
0.21
-0.7
0.17
-1.22
ns
0.09
Suprailiac skinfold (mm)
9.4 ± 3.4
10.4 ± 3.8
-0.97
3.02
0.49
-1.97
0.01
-1.99
ns
0.27
Mid-calf skinfold (mm)
10.2 ± 4.6
9.9 ± 3.6
0.30
2.34
0.37
-0.46
1.07
0.79
ns
0.07
Arm circumference (cm)
31.6 ± 2.9
31.8 ± 3.0
-0.16
1.62
0.26
-0.7
0.36
-0.62
ns
0.06
Leg circumference (cm)
36.7 ± 2.0
36.8 ± 2.1
-0.11
0.77
0.12
-0.37
0.13
-0.91
ns
0.06
Humerus diameter
6.77 ± 0.42
6.76 ± 0.40
0.00
0.15
0.02
-0.04
0.05
0.21
ns
0.01
Femur diameter
9.76 ± 0.53
9.69 ± 0.52
0.06
0.17
0.02
0.01
0.12
2.4
ns
0.13
Endomorphic component
3.12 ± 0.96
3.32 ± 1.00
-0.20
0.55
0.08
-0.38
-0.02
-2.32
ns
0.21
Mesomorphic component
5.07 ± 0.96
5.10 ± 0.93
-0.02
0.39
0.06
-0.15
0.10
-0.41
ns
0.03
Ectomorphic component
2.51 ± 0.76
2.44 ± 0.77
0.06
0.27
0.04
-0.02
0.15
1.39
ns
0.08
12MRT (m)
3100.8 ± 348.6
2978.1 ± 364.7
122
115
18.6
84.9
160.5
6.57
0.34
VO2 max (mLO2kg–1min–1)
56.6 ± 6.9
54.2 ± 7.2
2.45
2.3
0.37
1.69
3.21
6.57
0.34
SD: standard deviation; SEM: standard error of the mean; WHI: waist-hip index; WHeI: waist-height index; BMI: muscle mass index; kg/m2: kilograms per square
meters; 12MRT: 12-minute race test; mm: millimeters; cm: centimeters; m: meters; VO2 max: maximum oxygen consumption; mLO2kg–1min–1: milliliters of oxygen
per kilogram of body mass per minute
p < 0.002; ns: not significant; d: Cohen’s d.
https://doi.org/10.1371/journal.pone.0251516.t002
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
6 / 15
training program, while the control group (CG) executed a free training program. At the end
of the research, the EG decreased from 57.66 ± 2.56 to 56.85 ± 2.52 mLO2kg-1min-1. In con-
trast, the CG decreased from 58.08 ± 2.60 to 54.52 ± 2.80 mLO2kg-1min-1. Additionally, the
researchers reported significant decreases in VO2 max when comparing the EG to the CG in
the post-test (t = 16.06; p < 0.0001). Likewise, the endomorphic somatotype has a greater fat
mass than the mesomorphic and ectomorphic somatotype [43], and subjects with endomor-
phic predominance have shown a lower VO2 max than subjects with a mesomorphic or
ectomorphic predominance (endomorphic: 37.3 ± 0.77; mesomorphic: 40.2 ± 0.46; and ecto-
morphic: 43.5 ± 0.52) [51]. For this reason, the increase in the endomorphic component
observed in naval cadets after 12 weeks without mandatory physical training could condition
the decrease of VO2 max at the end of this period (p < 0.001, TE = 0.34). However, it is impor-
tant to analyze the ES for each variable studied, which allows us to observe each phenomenon’s
degree of presence, independent of the alpha level calculated [52]. In this study, like in research
by Parpa & Michaelides [24], all ES in the tests with significant differences in VO2 max, includ-
ing men and all data analysis, oscillated between 0.2–0.6. This was considered a small effect.
Fig 2. Changes in VO2 max and anthropometric parameters before and after 12 weeks without mandatory physical training. 12MRT: 12-minute race test;
mLO2Kg–1min–1: milliliters of oxygen per kilogram of body mass per minute; mm: millimeters; cm: centimeters; kg: kilograms; : p < 0.002.
https://doi.org/10.1371/journal.pone.0251516.g002
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
7 / 15
On the other hand, the significant differences in women had an ES between 0.6–1.2 (which
was considered as a moderate effect). Furthermore, the large and negative correlation between
VO2 max and the fat percentage observed in the test (r = -0.69, p = 0.01) increased after the
period without mandatory physical training (r = -0.75, p = 0.01). Up to this point, the decrease
in VO2 max has been attributed to two leading causes; on the one hand, a transition period
without mandatory and controlled physical training, while on the other hand, an increase in
fat mass, reflected in the endomorphic component of naval cadets [51].
Periods without physical training have also been associated with a decrease in muscle cross-
section [34]. This unfavorable consequence could be related to lower levels of muscle strength
[35]. In this case, Koundourakis et al. [31] examined the effects of six weeks without physical
training on performance parameters in soccer players; at the end of the study, the researchers
reported significant decreases in both squat jump (Team A: 39.70 ± 3.32 vs 37.30 ± 3.08 kg;
p < 0.001; Team B: 41.04 ± 3.34 vs 38.18 ± 3.03 kg; p < 0.001) and countermovement jump
(Team A: 41.04 ± 3.99 vs 39.13 ± 3.26%; p < 0.001); Team B: 42.82 ± 3.60 vs 40.09 ± 2.79 kg;
p < 0.001) in both experimental groups. The researchers also concluded that the observed
reductions in jumping ability (considered to be a negative effect) could be related to mis-
matches of rapidly contracting muscle fibers [25, 53]. In parallel, the endomorphic somatotype
has lesser muscle mass than the mesomorphic and ectomorphic somatotype [43]. In turn, Mir-
oshnichenko et al. [51] showed a high correlation between the predominance of the mesomor-
phic component and VO2 max. Likewise, an increase in the endomorphic component and
lower muscle mass could be associated with a lower VO2 max of the participants. Therefore,
Fig 3. Somatotype before and after 12 weeks without mandatory physical training.
https://doi.org/10.1371/journal.pone.0251516.g003
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
8 / 15
an increment of the endomorphic component in naval cadets may decrease the lower extremi-
ties’ strength, generating biomechanical and neuronal changes [54]. These last changes could
affect the economy of the race [55] and, consequently, decrease the performance in 12MRT
(p < 0.001, ES = 0.34). Although the evidence shows the negative influence of periods without
training on strength and muscular power [31, 35], mainly due to loss of muscle mass [34, 51],
the present study did not consider assessing naval cadets’ anaerobic capacity. Therefore, the
possible effects of 12 weeks without mandatory physical training on strength or power in both
the lower and upper extremities should be considered in future studies.
On the other hand, this study also showed increases in some anthropometric parameters
after 12 weeks without mandatory physical training, specifically in the tricipital skinfold thick-
ness in men (p = 0.02, ES = 0.18), arm circumference in women (p = 0.04, ES = 0.19) and the
endomorphic component in both men and women (p = 0.02, ES = 0.25). In this sense, evi-
dence shows that a period without physical training leads to increased fat mass and a decreased
lean mass [31–33]. Also, the tricipital fold, together with the subscapular and suprailiac folds,
are anthropometric indicators with a high explanatory power of VO2 max in both sexes [56].
We evidenced that those naval cadets with a higher tricipital fold had a reduced VO2 max
Fig 4. Correlation between VO2 max and anthropometric parameters before and after 12 weeks without mandatory physical training.
mLO2Kg–1min–1: milliliters of oxygen per kilogram of body mass per minute; % fat: percentage of fat; mm: millimeter.
https://doi.org/10.1371/journal.pone.0251516.g004
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
9 / 15
(Test: r = 0.76, p = 0.01; post test: r = 0.81, p = 0.01). Likewise, an elevated tricipital fold condi-
tions an elevated endomorphic component [42]. Consequently, anthropometric parameters
influence cardiorespiratory fitness, independent of sex, age, and obesity level [57]. Related to
this, Sotiropoulos et al. [33] evaluated changes in body weight and body fat percentage after a
four-week transition period in soccer players (The EG conducted a directed training program
and the CG a free training program). At the end of the study, the EG increased from 78.14 ±
4.77 to 78.74 ± 5.00 kg, while the CG increased from 76.48 ± 2.65 to 77.90 ± 2.82 kg (t = -4.91;
p < 0.005); and, also reported increased percentage of body fat (EG from 7.92 ± 1.68 to
8.17 ± 1.81%; CG from 7.77 ± 1.79 to 8.59 ± 1.80%; t = -8.42; p < 0.005). On the other hand,
Ormsbee et al. [58] examined the effect of five weeks without physical training on body com-
position in swimmers. At the end of the study, significant differences were observed in body
weight (68.96 ± 9.7 vs. 69.8 ± 9.8 kg; p = 0.03), fat mass (14.7 ± 7.6 vs. 16.5 ± 7.4 kg; p = 0.001),
and waist circumference (72.7 ± 3.1 vs. 73.8 ± 3.6 cm; p = 0.03). Also, Koundourakis et al. [31]
examined the effects of six weeks without physical training on the body composition of soccer
players; at the end of the study, the researchers reported significant increases in both body
weight (Team A: 77.60 ± 5.88 vs. 79.13 ± 6.16 kg; p < 0.001; Team B: 77.89 ± 8.75 vs.
79.49 ± 8.95 kg; p < 0.001) and in the fat percentage (Team A: 9.2 ± 3.33 vs. 11.01 ± 4.11%;
p < 0.001; Team B: 9.43 ± 3.55 vs. 10.40 ± 4.08 kg; p < 0.001) in both experimental groups.
Although some studies have established the body composition of armed forces personnel in
some countries [59] and anthropometric changes have been documented concerning soldiers’
physical training [60], the effects of 12 weeks without mandatory physical training on anthro-
pometric parameters have not been reported for naval cadets. Consequently, in connection
with the studies referred to above, our study’s findings show the importance of verifying and
controlling body composition after a period without mandatory physical training in naval
cadets [61], especially somatotype indicators [43]. However, it is essential to mention that the
present study did not control the participants’ caloric intake [62]. For this reason, we are not
sure that the changes in anthropometric parameters were only due to a decrease in physical
training [63–65]; there is a possibility that higher caloric intake, above the daily energy needs,
has also influenced these physical changes [62, 66].
Finally, the data show that VO2 max is an essential parameter of the physical condition
[38], and a higher VO2 max allows the efficient performance of physical tasks associated with
military personnel [13, 60]. It has also been demonstrated that subjects with a higher percent-
age of body fat have lower VO2 max, lower strength levels, and lower fatigue tolerance [67]. As
demonstrated in this study, a vacation period without mandatory physical training generates
decreases in the VO2 max [37] and negatively affects anthropometric parameters [51]. There-
fore, the vacation periods must be adapted into a transition phase [24, 25]. In this way, with
controlled and directed physical training, both athletes and naval cadets will have optimal
physical recovery and maintenance; this condition will allow them to face better the next cycle
of physical training [23].
One of the limitations of this study was the sample used. As mentioned above, the sample
was by convenience, which would not allow us to generalize the data. However, armed forces
personnel are more homogeneous in body structure [68] and eating behavior [69]. For this
reason, in this specific case, the results could be generalized to this population.
Conclusions
Twelve weeks without mandatory physical training significantly decreases the VO2 max in
naval cadets from 18 to 25 years old. Simultaneously, the same period without mandatory
training increases skinfold thickness and the endomorphic component in this population.
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
10 / 15
Practical applications
After evidence of decreases in VO2 max and negative increases in some anthropometric
parameters after 12 weeks without mandatory physical training, it is suggested that training
loads in the transition phase [25], whether due to vacations [28] or to unforeseen events [30].
Acknowledgments
We thank the 38 naval cadets for their voluntary and disinterested participation in the Arturo
Prat Naval Academy.
Author Contributions
Conceptualization: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Data curation: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Formal analysis: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Funding acquisition: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Investigation: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Methodology: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Resources: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames Maliqueo.
Supervision: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames Maliqueo.
Validation: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames Maliqueo.
Visualization: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Galdames
Maliqueo.
Writing – original draft: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Gal-
dames Maliqueo.
Writing – review & editing: A´lvaro Huerta Ojeda, Guillermo Barahona-Fuentes, Sergio Gal-
dames Maliqueo.
References
1.
Ojeda A´ H, Rı´os LC, Barrilao RG, Rios IC, Serrano PC. Effect of variable resistance on post-activation
potentiation: A systematic review. Arch Med Deporte. 2016; 33(5):338–45.
2.
Barahona-Fuentes G, Huerta Ojeda A´ , Galdames Maliqueo S. The influence of High-Intensity Interval
Training Based Plyometric Exercise on Jump Height and Peak Power of Under-17 Male Soccer Players.
Educacio´n Fı´sica y Ciencia. 2019; 21(2):e080. https://doi.org/10.24215/23142561e080.
3.
Huerta A´ C, Galdames S, Cataldo M, Barahona G, Rozas T, Ca´ceres P. Effects of a high intensity inter-
val training on the aerobic capacity of adolescents. Rev Med Chil. 2017; 145(8):972–9. https://doi.org/
10.4067/s0034-98872017000800972 PMID: 29189854
4.
Gacesa JZ, Jakovljevic DG, Kozic DB, Dragnic NR, Brodie DA, Grujic NG. Morpho-functional response
of the elbow extensor muscles to twelve-week self-perceived maximal resistance training. Clin Physiol
Funct Imaging. 2010; 30(6):413–9. https://doi.org/10.1111/j.1475-097X.2010.00957.x PMID: 20670339
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
11 / 15
5.
Ingle L, Stephenson A, Sandercock GR. Physical activity profiles and selected muscular fitness vari-
ables in English schoolchildren: A north–south divide? Eur J Sport Sci. 2016; 16(8):1187–96. https://
doi.org/10.1080/17461391.2016.1183714 PMID: 27220086
6.
Sabido R, Peñaranda M, Herna´ndez-Davo´ JL. Comparison of acute responses to four different hyper-
trophy-oriented resistance training methodologies. Eur J Hum Mov. 2016;37109–21.
7.
Cordova A, Villa G, Sureda A, Rodriguez-Marroyo JA, Sa´nchez-Collado MP. Physical Activity and Car-
diovascular Risk Factors in Spanish Children Aged 11–13 Years. Rev Española Cardiol. 2012; 65
(7):620–6. https://doi.org/10.1016/j.recesp.2012.01.026 PMID: 22633280
8.
Ga´lvez Casas A, Rodrı´guez Garcı´a PL, Garcı´a-Canto´ E, Rosa Guillamo´n A, Pe´rez-Soto JJ, Tarraga
Marcos L, et al. Aerobic capacity and quality of life in school children from 8 to 12. Clin Investig Arterios-
cler. 2015; 27(5):239–45. https://doi.org/10.1016/j.arteri.2015.01.001 PMID: 25814171
9.
Patel A V., Hodge JM, Rees-Punia E, Teras LR, Campbell PT, Gapstur SM. Relationship between mus-
cle-strengthening activity and cause-specific mortality in a large US cohort. Prev Chronic Dis.
2020;171–9. https://doi.org/10.5888/pcd17.190408.
10.
Ojeda A´ H, Rı´os LC, Barrilao RG, Serrano PC. Acute effect of a complex training protocol of back squats
on 30-m sprint times of elite male military athletes. J Phys Ther Sci. 2016; 28(3):752–6. https://doi.org/
10.1589/jpts.28.752 PMID: 27134353
11.
Webber BJ, Flower AM, Pathak SR, Burganowski RP, Pawlak MT, Gottfredson RC, et al. Physical and
Mental Health of US Air Force Military Training Instructors. Mil Med. 2019; 184(5–6):e248–54. https://
doi.org/10.1093/milmed/usy418 PMID: 30690457
12.
Vrijkotte S, Roelands B, Pattyn N, Meeusen R. The Overtraining Syndrome in Soldiers: Insights from
the Sports Domain. Mil Med. 2019; 184(5–6):e192–200. https://doi.org/10.1093/milmed/usy274 PMID:
30535270
13.
Taylor MK, Markham AE, Reis JP, Padilla GA, Potterat EG, Drummond SPA, et al. Physical fitness
influences stress reactions to extreme military training. Mil Med. 2008; 173(8):738–42. https://doi.org/
10.7205/milmed.173.8.738 PMID: 18751589
14.
Schneider KL, Spring B, Pagoto SL. Exercise and energy intake in overweight, sedentary individuals.
Eat Behav. 2009; 10(1):29–35. https://doi.org/10.1016/j.eatbeh.2008.10.009 PMID: 19171314
15.
Lovell DI, Cuneo R, Wallace J, McLellan C. The hormonal response of older men to sub-maximum aero-
bic exercise: The effect of training and detraining. Steroids. 2012; 77(5):413–8. https://doi.org/10.1016/
j.steroids.2011.12.022 PMID: 22248672
16.
Stebbings GK, Morse CI, McMahon GE, Onambele GL. Resting arterial diameter and blood flow
changes with resistance training and detraining in healthy young individuals. J Athl Train. 2013; 48
(2):209–19. https://doi.org/10.4085/1062-6050-48.1.17 PMID: 23672385
17.
Mujika I. The influence of training characteristics and tapering on the adaptation in highly trained individ-
uals: A review. Int J Sports Med. 1998; 19(7):439–46. https://doi.org/10.1055/s-2007-971942 PMID:
9839839
18.
Flann KL, Lastayo PC, McClain DA, Hazel M, Lindstedt SL. Muscle damage and muscle remodeling:
No pain, no gain? J Exp Biol. 2011; 214(4):674–9. https://doi.org/10.1242/jeb.050112.
19.
Gunter K, Baxter-Jones ADG, Mirwald RL, Almstedt H, Fuchs RK, Durski S, et al. Impact exercise
increases BMC during growth: an 8-year longitudinal study. J Bone Miner Res. 2008; 23(7):986–93.
https://doi.org/10.1359/jbmr.071201 PMID: 18072874
20.
Maroto-Izquierdo S, Garcı´a-Lo´pez D, Fernandez-Gonzalo R, Moreira OC, Gonza´lez-Gallego J, de Paz
JA. Skeletal muscle functional and structural adaptations after eccentric overload flywheel resistance
training: a systematic review and meta-analysis. J Sci Med Sport. 2017; 20(10):943–51. https://doi.org/
10.1016/j.jsams.2017.03.004 PMID: 28385560
21.
Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee IM, et al. Quantity and quality of
exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in
apparently healthy adults: Guidance for prescribing exercise. Med Sci Sports Exerc. 2011; 43(7):1334–
59. https://doi.org/10.1249/MSS.0b013e318213fefb PMID: 21694556
22.
Barahona-Fuentes G, Ojeda A´ H, Jerez-Mayorga D. Effects of different methods of strength training on
indicators of muscle fatigue during and after strength training: a systematic review. Motriz J Phys Educ.
2020; 26(3):e10200063. https://doi.org/10.1590/S1980-6574202000030063.
23.
Silva JR, Brito J, Akenhead R, Nassis GP. The transition period in soccer: a window of opportunity.
Sport Med. 2016; 46(3):305–13. https://doi.org/10.1007/s40279-015-0419-3 PMID: 26530720
24.
Parpa K, Michaelides MA. The effect of transition period on performance parameters in elite female soc-
cer players. Int J Sports Med. 2020; 41(8):528–32. https://doi.org/10.1055/a-1103-2038 PMID:
32059247
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
12 / 15
25.
Mujika I, Padilla S. Detraining: loss of training-induced physiological and performance adaptations. Part
I. Sport Med. 2000; 30(2):79–87. https://doi.org/10.2165/00007256-200030020-00002.
26.
Musumeci G. Sarcopenia and exercise “the state of the art.” J Funct Morphol Kinesiol. 2017; 2(4):.
https://doi.org/10.3390/jfmk2040040.
27.
Maugeri G, Castrogiovanni P, Battaglia G, Pippi R, D’Agata V, Palma A, et al. The impact of physical
activity on psychological health during Covid-19 pandemic in Italy. Heliyon. 2020; 6(6):e04315. https://
doi.org/10.1016/j.heliyon.2020.e04315 PMID: 32613133
28.
Katzmarzyk PT, Barreira T V., Broyles ST, Champagne CM, Chaput JP, Fogelholm M, et al. Physical
activity, sedentary time, and obesity in an international sample of children. Med Sci Sports Exerc. 2015;
47(10):2062–9. https://doi.org/10.1249/MSS.0000000000000649 PMID: 25751770
29.
Prentice-Dunn H, Prentice-Dunn S. Physical activity, sedentary behavior, and childhood obesity: a
review of cross-sectional studies. Psychol Health Med. 2012; 17(3):255–73. https://doi.org/10.1080/
13548506.2011.608806 PMID: 21995842
30.
Paoli A, Musumeci G. Elite athletes and COVID-19 lockdown: future health concerns for an entire sec-
tor. J Funct Morphol Kinesiol. 2020; 5(2):10–2. https://doi.org/10.3390/jfmk5020030 PMID: 33467246
31.
Koundourakis NE, Androulakis NE, Malliaraki N, Tsatsanis C, Venihaki M, Margioris AN. Discrepancy
between exercise performance, body composition, and sex steroid response after a six-week detraining
period in professional soccer players. PLoS One. 2014; 9(2):. https://doi.org/10.1371/journal.pone.
0087803.
32.
Reinke S, Karhausen T, Doehner W, Taylor W, Hottenrott K, Duda GN, et al. The influence of recovery
and training phases on body composition, peripheral vascular function and immune system of profes-
sional soccer players. PLoS One. 2009; 4(3):1–7. https://doi.org/10.1371/journal.pone.0004910.
33.
Sotiropoulos AS, Travlos AK, Gissis I, Souglis AG, Grezios A. The effect of a 4-week training regimen
on body fat and aerobic capacity of professional soccer players during the transition period. J Strength
Cond Res. 2009; 23(6):1697–703. https://doi.org/10.1519/JSC.0b013e3181b3df69 PMID: 19675494
34.
Hakkinen K. Effect of combined concentric and eccentric strength training and detraining on force-time,
muscle fiber and metabolic characteristics of leg extensor muscles. Scand J Sport Sci. 1981;350–8.
35.
Izquierdo M, Ibanez J, Gonzalez-Badillo JJ, Ratamess N, Kraemer WJ, Hakkinen K, et al. Detraining
and tapering effects on hormonal responses and strength performance. J Strenght Cond Res. 2007; 21
(3):768–75. https://doi.org/10.1519/R-21136.1 PMID: 17685721
36.
De Paiva PRV, Casalechi HL, Tomazoni SS, MacHado CDSM, Ribeiro NF, Pereira AL, et al. Does the
combination of photobiomodulation therapy (PBMT) and static magnetic fields (sMF) potentiate the
effects of aerobic endurance training and decrease the loss of performance during detraining? A rando-
mised, triple-blinded, placebo-controlled trial. BMC Sports Sci Med Rehabil. 2020; 12(1):1–11. https://
doi.org/10.1186/s13102-020-00171-2.
37.
Liguori G, Krebsbach K, Schuna J. Decreases in maximal oxygen uptake among army reserve officers’
training corps cadets following three months without mandatory physical training. Int J Exerc Sci. 2012;
5(4):354–9. PMID: 27182392
38.
Ojeda A´ H, Maliqueo SG, Serrano PC. Validacio´n del test de 6 minutos de carrera como predictor del
consumo ma´ximo de oxı´geno en el personal naval. Rev Cuba Med Mil. 2017; 46(4):1–11.
39.
Galdames S, Huerta A´ , Pastene A. Effect of acute sodium bicarbonate supplementation on perfor-
mance on the obstacle run in professional military pentathlete. Arch Med Deporte. 2020; 37(4):220–6.
40.
Armada-de-Chile. ¿Quie´nes la componen? Armada de Chile. 2014;
41.
Ato M, Lo´pez JJ, Benavente A. A classification system for research designs in psychology. An Psicol.
2013; 29(3):1038–59. https://doi.org/10.6018/analesps.29.3.178511.
42.
Berral F. Protocolo de medidas antropome´tricas. Jornadas Me´dico Sanit. sobre Atlet., 2004;, p. 115–
22.
43.
Carter JEL, Heath BH. Somatotyping: development and applications. vol. 5. New York, USA: Cam-
bridge university press; 1990;
44.
National Health and Nutrition Examination Survey. Anthropometry procedures manual. 2005;
45.
Durnin J, Womersley J. Body fat assessed from total body density and its estimation from skinfold thick-
ness: measurements on 481 men and women aged from 16 to 72 years. Br J Nutr. 1974;3277–97.
https://doi.org/10.1079/bjn19740060 PMID: 4843734
46.
Barrera A, Gladys M. Esta´ndares antropome´tricos para evaluacio´n del estado nutritivo. INTA. Santi-
ago, Chile: 2004;
47.
Mederico M, Paoli M, Zerpa Y, Briceño Y, Go´mez-Pe´rez R, Martı´nez JL, et al. Reference values of
waist circumference and waist/hip ratio in children and adolescents of Me´rida, Venezuela: comparison
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
13 / 15
with international references. Endocrinol y Nutr. 2013; 60(5):235–42. https://doi.org/10.1016/j.endoen.
2012.12.006.
48.
Cooper KH. A means of assessing maximal oxygen intake: correlation between field and treadmill test-
ing. Jama. 1968; 203(3):201–4. PMID: 5694044
49.
Hopkins WG, Marshall SW, Batterham AM, Hanin J. Progressive statistics for studies in sports medicine
and exercise science. Med Sci Sports Exerc. 2009; 41(1):3–12. https://doi.org/10.1249/MSS.
0b013e31818cb278 PMID: 19092709
50.
Martı´nez Camblor P. P-value adjustment for multiple comparisons. Rev Chil Salud Pu´blica. 2012; 16
(3):225–32. https://doi.org/10.5354/0717-3652.2012.23127.
51.
Miroshnichenko VM, Furman YM, Brezdeniuk OY, Onyshchuk VE, Gavrylova N V, Salnykova S-V. Cor-
relation of maximum oxygen consumption with component composition of the body, body mass of men
with different somatotypes aged 25–35. Pedagog Phys Cult Sport. 2020; 24(2):290–6. https://doi.org/
10.15561/26649837.2020.0603.
52.
Casado A, Prieto L, Alonso J. El tamaño del efecto de la diferencia entre dos medias: ¿estadı´stica-
mente significativo o clı´nicamente relevante? Med Clin (Barc). 1999; 112(15):584–8. PMID: 10365387
53.
Perez-Gomez J, Rodriguez GV, Ara I, Olmedillas H, Chavarren J, Gonza´lez-Henriquez JJ, et al. Role of
muscle mass on sprint performance: gender differences? Eur J Appl Physiol. 2008; 102(6):685–94.
https://doi.org/10.1007/s00421-007-0648-8 PMID: 18084774
54.
Trowell D, Vicenzino B, Saunders N, Fox A, Bonacci J. Effect of strength training on biomechanical and
neuromuscular variables in distance runners: a systematic review and meta-analysis. Sport Med. 2020;
50(1):133–50. https://doi.org/10.1007/s40279-019-01184-9 PMID: 31541409
55.
Skovgaard C, Christensen PM, Larsen S, Andersen TR, Thomassen M, Bangsbo J. Concurrent speed
endurance and resistance training improves performance, running economy, and muscle NHE1 in mod-
erately trained runners. J Appl Physiol. 2014; 117(10):1097–109. https://doi.org/10.1152/japplphysiol.
01226.2013 PMID: 25190744
56.
de Andrade E, Gimenes H, Santos D. Which body fat anthropometric indicators are most strongly asso-
ciated with maximum oxygen uptake in adolescents? Asian J Sports Med. 2017; 8(3):e13812. https://
doi.org/10.5812/asjsm.13812.
57.
Yanek LR, Vaidya D, Kral BG, Dobrosielski DA, Moy TF, Stewart KJ, et al. Lean mass and fat mass as
contributors to physical fitness in an overweight and obese african american population. Ethn Dis. 2015;
25(2):214–9. PMID: 26118151
58.
Ormsbee MJ, Arciero P. Detraining increases body fat and weight and decreases VO2peak and meta-
bolic rate. J Strength Cond Res. 2012; 26(8):2087–95. https://doi.org/10.1519/JSC.
0b013e31823b874c PMID: 22027854
59.
Nelson R, Cheatham J, Gallagher D, Bigelman K, Thomas DM. Revisiting the United States Army body
composition standards: a receiver operating characteristic analysis. Int J Obes. 2019; 43(8):1508–15.
https://doi.org/10.1038/s41366-018-0195-x PMID: 30181655
60.
Dyrstad SM, Soltvedt R, Halle´n J. Physical fitness and physical training during norwegian military ser-
vice. Mil Med. 2006; 171(8):736–41. https://doi.org/10.7205/milmed.171.8.736 PMID: 16933814
61.
Pl¸avin¸a L, Umbrasˇko S. Analysis of physical fitness tests and the body composition of the military per-
sonnel. Pap Anthropol. 2016; 25(1):27. https://doi.org/10.12697/poa.2016.25.1.03.
62.
Thomas DT, Erdman KA, Burke LM. Position of the academy of nutrition and dietetics, dietitians of can-
ada, and the american college of sports medicine: nutrition and athletic performance. J Acad Nutr Diet.
2016; 116(3):501–28. https://doi.org/10.1016/j.jand.2015.12.006 PMID: 26920240
63.
Franckle R, Adler R, Davison K. Accelerated weight gain among children during summer versus school
year and related racial/ethnic disparities: a systematic review. Prev Chronic Dis. 2014; 11(12):1–10.
https://doi.org/10.5888/pcd11.130355 PMID: 24921899
64.
Moreno JP, Johnston CA, Woehler D. Changes in weight over the school year and summer vacation:
results of a 5-year longitudinal study. J Sch Health. 2013; 83(7):473–7. https://doi.org/10.1111/josh.
12054 PMID: 23782089
65.
von Hippel PT, Workman J. From kindergarten through second grade, U.S. children’s obesity preva-
lence grows only during summer vacations. Obesity. 2016; 24(11):2296–300. https://doi.org/10.1002/
oby.21613 PMID: 27804271
66.
Cooper JA, Tokar T. A prospective study on vacation weight gain in adults. Physiol Behav.
2016;15643–7. https://doi.org/10.1016/j.physbeh.2015.12.028 PMID: 26768234
67.
Crawford K, Fleishman K, Abt JP, Sell TC, Lovalekar M, Nagai T, et al. Less body fat improves physical
and physiological performance in army soldiers. Mil Med. 2011; 176(1):35–43. https://doi.org/10.7205/
milmed-d-10-00003 PMID: 21305957
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
14 / 15
68.
Maldonado I, Calero S. Anthropometric profile and body composition in aspirants of the Army Soldiers
Training School. Rev Cuba Investig Biome´dicas. 2017; 36(2):1–13.
69.
Kildal CL, Syse KL. Meat and masculinity in the Norwegian Armed Forces. Appetite. 2017; 112(Novem-
ber 2013):69–77. https://doi.org/10.1016/j.appet.2016.12.032 PMID: 28040506
PLOS ONE
Period without physical training on maximum oxygen uptake
PLOS ONE | https://doi.org/10.1371/journal.pone.0251516
June 2, 2021
15 / 15
(...TRUNCATED) | Effects of a period without mandatory physical training on maximum oxygen uptake and anthropometric parameters in naval cadets.(...TRUNCATED) | 06-02-2021 | Huerta Ojeda, Álvaro,Barahona-Fuentes, Guillermo,Galdames Maliqueo, Sergio(...TRUNCATED) | eng |
PMC10703220 | Reference number: PONE-D-23-18858 (previous submission PONE-D-23-16206)
Exploring running styles in the field through cadence and duty factor modulation
Dear dr. L. A. Peyré-Tartaruga and editorial office,
Thank you for evaluating our manuscript and for giving us the opportunity to resubmit.
We have made the following changes to the manuscript in response to the concerns of the editorial
office:
-
We have included the reference numbers of both the original ethical application (VCWE-2019–
006R1) and the amendment (VCWE-2021-043) in the method section of the manuscript.
-
We have included the original ethical application (VCWE-2019–006R1) in Dutch, with the English
translations in comments in the pdf file.
-
We have included the amendment (VCWE-2021-043) in Dutch, with the English translations in
comments in the pdf file.
-
We have included the approval emails from our IRB for both the original ethical application
(VCWE-2019–006R1) and the amendment (VCWE-2021-043).
-
We have included the informed consent form for this study in English.
-
We have included the participant information form for this study in English.
We believe that by making those changes and including the additional files we have addressed the
concerns of the editorial office. Please find below the message from the editorial office.
Thank you for your time and consideration.
Sincerely,
Anouk Nijs, Msc.
[email protected]
Dr. Melvyn Roerdink
[email protected]
Prof. Dr. Peter J. Beek
[email protected]
Department of Human Movement Sciences, Faculty of Behavioural and Movement Sciences,
Vrije Universiteit Amsterdam, The Netherlands
PONE-D-23-16206
Exploring running styles in the field through cadence and duty factor modulation PLOS ONE
Dear Dr. Nijs,
I am writing to you about your appeal on the editorial decision for your submission to PLOS ONE above.
After careful consideration of the manuscript, the reasons for the previous rejection, and your reasons
for appealing, we are upholding the decision to reject the manuscript.
As you are aware, manuscripts submitted to PLOS ONE are assessed based on the journal’s publication
criteria. We have concerns on the contents of the manuscript including that the approval document
provided did not match the study presented in the manuscript. Furthermore, the approval number on
the manuscript (VCWE-2019–006R1) did not match the one provided in the email from your IRB (VCWE-
2021-043)
Considering those concerns, the manuscript does not currently meet our criteria for publication
requiring that the research meets all applicable standards for the ethics of experimentation and
research integrity.
However, if you are able to provide a copy of the original approval document issued by your IRB (i.e.
VCWE-2019–006R1) and an English translation, as well as the documents that you have mentioned in
your appeal email, we do feel that a revised manuscript may be suitable for consideration. This would
however need to be considered as a new submission.
If you are able to revise the manuscript as indicated above and submit a new manuscript to PLOS ONE,
please refer to the original submission in the cover letter.
Thank you for your interest in PLOS ONE.
Best wishes,
Anushmathi PM
Editorial Office
PLOS ONE
(...TRUNCATED) | Exploring running styles in the field through cadence and duty factor modulation.(...TRUNCATED) | 12-07-2023 | Nijs, Anouk,Roerdink, Melvyn,Beek, Peter Jan(...TRUNCATED) | eng |
PMC7309010 | sensors
Article
Effects of Novel Inverted Rocker Orthoses for First
Metatarsophalangeal Joint on Gastrocnemius Muscle
Electromyographic Activity during Running:
A Cross-Sectional Pilot Study
Rubén Sánchez-Gómez 1
, Carlos Romero-Morales 2,*
, Álvaro Gómez-Carrión 1,
Blanca De-la-Cruz-Torres 3
, Ignacio Zaragoza-García 1
, Pekka Anttila 4, Matti Kantola 4 and
Ismael Ortuño-Soriano 1
1
Nursing Department, Faculty of Nursing, Physiotherapy and Podiatry, Universidad Complutense de
Madrid, 28040 Madrid, Spain; [email protected] (R.S.-G.); [email protected] (Á.G.-C.);
[email protected] (I.Z.-G.); [email protected] (I.O.-S.)
2
Faculty of Sport Sciences, Universidad Europea de Madrid, Villaviciosa de Odón, 28670 Madrid, Spain
3
Department of Physiotherapy, University of Seville, c/Avicena, s/n, 41009 Seville, Spain; [email protected]
4
Applied Science of Metropolia Univesity, Podiatry Department, 01600 Helsinki, Finland;
pekka.anttila@metropolia.fi (P.A.); Matti.Kantola@metropolia.fi (M.K.)
*
Correspondence: [email protected]
Received: 15 April 2020; Accepted: 3 June 2020; Published: 5 June 2020
Abstract: Background: The mobility of the first metatarsophalangeal joint (I MPTJ) has been related
to the proper windlass mechanism and the triceps surae during the heel-off phase of running gait;
the orthopedic treatment of the I MPTJ restriction has been made with typical Morton extension
orthoses (TMEO). Nowadays it is unclear what effects TMEO or the novel inverted rocker orthoses
(NIRO) have on the EMG activity of triceps surae during running. Objective: To compare the TMEO
effects versus NIRO on EMG triceps surae on medialis and lateralis gastrocnemius activity during
running. Study design: A cross-sectional pilot study. Methods: 21 healthy, recreational runners were
enrolled in the present research (mean age 31.41 ± 4.33) to run on a treadmill at 9 km/h using aleatory
NIRO of 6 mm, NIRO of 8 mm, TMEO of 6 mm, TMEO of 8 mm, and sports shoes only (SO), while
the muscular EMG of medial and lateral gastrocnemius activity during 30 s was recorded. Statistical
intraclass correlation coefficient (ICC) to test reliability was calculated and the Wilcoxon test of all five
different situations were tested. Results: The reliability of values was almost perfect. Data showed
that the gastrocnemius lateralis increased its EMG activity between SO vs. NIRO-8 mm (22.27 ± 2.51
vs. 25.96 ± 4.68 mV, p < 0.05) and SO vs. TMEO-6mm (22.27 ± 2.51 vs. 24.72 ± 5.08 mV, p < 0.05).
Regarding gastrocnemius medialis, values showed an EMG notable increase in activity between SO
vs. NIRO-6mm (22.93 ± 2.1 vs. 26.44 ± 3.63, p < 0.001), vs. NIRO-8mm (28.89 ± 3.6, p < 0.001), and vs.
TMEO-6mm (25.12 ± 3.51, p < 0.05). Conclusions: Both TMEO and NIRO have shown an increased
EMG of the lateralis and medialis gastrocnemius muscles activity during a full running cycle gait.
Clinicians should take into account the present evidence when they want to treat I MTPJ restriction
with orthoses, and consider the inherent triceps surae muscular cost relative to running economy.
Keywords: triceps surae; first metatarsophalangeal joint; surface electromyography
1. Introduction
Coterill [1] was the first author who described painful osteoarthritis (OA) of the first
metatarsophalangeal joint (IMTPJ), which is known as hallux rigidus (HR). HR is the last stage
Sensors 2020, 20, 3205; doi:10.3390/s20113205
www.mdpi.com/journal/sensors
Sensors 2020, 20, 3205
2 of 12
of the IMTPJ degeneration, with functional hallux limitus [2] (FHL) at the beginning of the pathological
progress [3]. Joint disease is thought to be caused by repetitive impacts on the dorsal aspect of the base
of the proximal phalanx of the hallux by the first metatarsal head during the propulsion phase of gait
and running in feet with multifactorial biomechanical and/or structural deficits [4]. The limitation
of IMTPJ has been linked to gait problems [5] and its consequences on ankle, knee, hip, or low back
during running [6].
The treatment of this injury has been addressed in several conservative non-surgical and surgical
ways.
Non-surgical management is valid to treat HR in the earliest stages [7,8] and includes
ultrasound therapy, infiltrative drugs, shoe modifications, hallux bandages, manual mobilization,
flexor strengthening, and orthoses to improve the joint problems. There are a few references on
treatment of OA using plantar insoles in HR and FHL. Traditional Morton’s extensions are orthoses
with a flat light modification under the first ray that has been used to treat HR [9–11] to avoid the
impact between the proximal phalanx and first metatarsal bones. This opens the IMTPJ dorsally but
restricts its dorsiflexion movement, while rocker-sole footwear modifications have shown a reduction
in the peak pressure under the IMTPJ. This decreases the average gait cycle that is spent in the stance
phase [12] and increases muscle activity of the lower limb [13]. However, there is no reference to either
the inverted rocker-sole orthoses effects or the effect of footwear modifications on muscle activity
during running.
On the other hand, running economy (RE) has been described as the oxygen cost of running at a
given speed in every case [14] and factors such as biomechanics and muscular fatigue can influence
the RE [15]. Additionally, barefoot running has shown differences in biomechanical behaviour [16]
and muscular responses [17,18] when it is compared with classical running shoes. Compared to
fatigue, strength training added to a normal training program for distance running can improve RE
between 2% and 8%. An increase in muscle mass training programs around the proximal region
of the lower limb, such as quadriceps or hamstring [19], or around the distal regions, such as the
triceps surae [20] with plantarflexion and dorsiflexion ankle exercises, has shown some benefits on RE.
Accordingly, triceps surae and its relationship with the windlass mechanism [21] in the propulsion
phase of gait and running has been reported to provide between 8% and 17% of the elastic energy
that is needed for the heel-off phase [22,23] toward a suitable IMTPJ dorsiflexion [24,25]. However,
the electromyography (EMG) effects in the triceps surae with limited dorsiflexion of the IMTPJ that
is induced by any orthotic dorsiflexion restriction has never been studied. Understanding the EMG
activity of this muscle will allow us to understand if the subjects could be increasing their energy cost
during running, which is very important for an efficient RE [19]. However, no previous research has
studied the effect of a novel inverted rocker orthoses (NIRO) on the EMG activity of the triceps surae
compared to traditional Morton’s extension orthoses (TMEO) during running in the healthy population.
Because of the restricting IMTPJ effect of TMEO and its influence on the windlass mechanism that is
linked with the triceps surae [24,25], we hypothesized that TMEO (6 mm and 8 mm) may increase
the EMG activity of the gastrocnemius medialis and lateralis muscles compared to the shoe only (SO)
condition during running activity; in addition, regarding previous muscular activity changes that are
reported with classical rocker soles [13], we hypothesized that NIRO (6 mm and 8 mm) may reduce the
EMG of gastrocnemius medialis and lateralis compared to TMEO (6 mm and 8 mm), and this may
increase EMG compared to SO in healthy people during running activity.
2. Materials and Methods
The public institutional review board at Virgen Macarena-Virgen del Rocío hospitals, reviewed
and approved the present study (certificate number f7f4a6567676d7ba7163bce0d15e7f98c9f33354).
Ethical and human criteria were followed according to the Declaration of Helsinki, and signed informed
consent was obtained from all subjects.
Sensors 2020, 20, 3205
3 of 12
2.1. Design and Sample Size
The statistics unit at the Spanish public university used software to assess the suitable sample
size to perform this cross-sectional observational study and to study the difference in the EMG
changes in the gastrocnemius medialis and lateralis muscles between SO, NIRO 6 mm, NIRO
8 mm, TMEO 6 mm, and TMEO 8 mm groups during running. Previous data on the triceps surae
showed 7.0 ± 0.6 millivolts (mV) wearing 9-mm heel lifts compared to 4.9 ± 0.6 mV wearing typical
shoes [26]. Taking into account a statistical power of 80%, β = 20%, a 95% confidence interval (CI), and
α = 0.05, 30 subjects were needed to complete the study. Considering the typical loss of 20% subjects,
24 participants were recruited. However, three individuals were excluded from the study because
they felt pain and discomfort during the EMG assessment. Reporting of Observational Studies in
Epidemiology (STROBE) [27] criteria and a randomly consecutive sampling technique were followed
to develop the present research.
2.2. Subjects
The following inclusion criteria were used to select the participants: (1) healthy participants,
between 18 and 30 years old; (2) recreational runners with 3–4 h of training per week with more than
1 year of experience; (3) neutral foot posture index (FPI) with values between 0 and +5 points according
to a validity tool [28]; and (4) no injuries or pain at the time of the test. The exclusion criteria were as
follows: (1) any lower limb injury during the last 6 months; (2) less movement in either foot joint than
what is required to perform the optimal biomechanics according to normal values [29,30]; or (3) under
the influence of any drugs effects at the time of the measurements. Body mass index (BMI) was taken
into account to select a homogeneous sample, using Quetelet’s equation as follows: BMI = weight
(kg)/height (m2) [31].
2.3. Instrumentation and Assessments
Neurotrac® Simplex Plus (Verity Medical Ltd., Braishfield, UK) EMG electronic device with a
USB-Bluetooth [32] was used to study the triceps surae activity during the running test. The recording
range on the device was 0.2 mV to 2000 mV, with a sensitivity of 0.1 mV RMS, 10 m of free wireless
(Bluetooth) connection range and an accuracy of 4% of the reading from mV +/− 0.3 mV to 200 Hz,
with a bandpass filter of 18 Hz +/− 4 Hz to 370 Hz +/− 10% for readings below 235 mV. The signal
was assessed using self-adhesive circular surface electrodes that were 30 mm in diameter and made of
high-quality hydrogel and conductive carbon film to detect the electrical action of the muscle fibers.
The signal from each electrode was captured by the receiver module and filtered automatically by the
Neurotrac® software (Verity Medical Ltd., Braishfield, UK). It was sent by a unidirectional radioelectric
secure connection to the computer and it was digitally transformed by the software to generate activity
patterns data for each electrode.
2.4. Materials
NIRO was made using a flat sheet of ethylene-vinyl acetate (EVA) with a semi-rigid density
that was 3 mm thick, without any orthotic element that could interface with normal biomechanical
behaviour of the foot. NIRO had an inverted rocker composed of EVA medium that was 5 cm long,
2 cm wide, and 6 mm thick. Its proximal and distal edges were smoothly polished, and it was placed
on the IMTPJ. The whole orthotic was covered with an EVA soft layer that was 1 mm thick (Figure 1).
The TMEO was made with the same flat sheet of semi-rigid EVA that was 3 mm thick without any
orthotic element and with a rectangular flat piece of EVA medium (6 mm thick) that was placed under
the IMTPJ area and it was covered with an EVA soft layer that was 1 mm thick (Figure 2). The neutral
SOs were “New Feel PW 100M medium grey” (ref. number: 2018022). NIRO and TMEO were made in
an external orthopedic laboratory that was blinded to the study protocol.
Sensors 2020, 20, 3205
4 of 12
Sensors 2020, 20, x FOR PEER REVIEW
4 of 12
Figure 1. Novel inverted rocker orthotic (NIRO).
A flat sheet of ethylene-vinyl acetate (EVA) with an inverted rocker piece of EVA medium 6
mm thick under IMTPJ (bulked raised shape) covered with a yellow EVA soft layer that was 1 mm
thick.
Figure 2. Typical Morton’s extension orthotic (TMEO).
A flat sheet of ethylene-vinyl acetate (EVA) with a rectangular flat piece of EVA medium 6 mm
thick under IMTPJ covered with a black EVA soft layer that was 1 mm thick.
2.5. Procedure
The podiatric clinician researcher (RSG) performed a physical assessment of the subjects and
applied the eligibility criteria. To visualize the muscle belly, each subject was asked to perform
plantarflexion of the ankle joint for a few seconds. The surface electrodes were then placed
longitudinally onto the most prominent bulge of the gastrocnemius medialis and lateralis, based on
the “European recommendations for surface EMG” [33]. The subjects were then asked to stand on
one leg in the tip-toe position using their dominant foot for 5 s to set the maximal voluntary
contractions that were needed in the strongest limb to calibrate the software and to normalize EMG
data amplitudes for each test [34]. This was followed by acclimatization of subjects to a motorized
treadmill at 5.17 km/h for 3 min [17]. The participants were divided randomly in gastrocnemius
lateralis or medialis group by choosing a sealed envelope that assigned them to one group or
another to begin the test; after that, they selected one of the five sealed envelopes with each of the
five different conditions of the study (SO, NIRO 6 mm, NIRO 8 mm, TMEO 6 mm, TMEO 8 mm) to
set randomly the order of the test. The 11 subjects who began with medialis gastrocnemius
assessments, did the lateralis test following the same randomized protocol for each of the five
different conditions and vice versa for the 12 participants who began with the lateralis test (Figure
3). Three running trials at 9 km/h [35] under five different conditions (SO, NIRO 6 mm, NIRO 8
mm, TMEO 6 mm, and TMEO 8 mm) on the same day were randomly performed. The duration of
each trial was 1 min. For each subject, the mean EMG muscle activity pattern [36] of the
gastrocnemius medialis of the dominant leg was recorded during the last 30 s of each 1-min trial,
which was performed three times, leaving 5 min of rest between each test [37]. To avoid a potential
imbalance, the same condition was added to contralateral foot. The same protocol was performed to
Figure 1. Novel inverted rocker orthotic (NIRO).
Sensors 2020, 20, x FOR PEER REVIEW
4 of 12
Figure 1. Novel inverted rocker orthotic (NIRO).
A flat sheet of ethylene-vinyl acetate (EVA) with an inverted rocker piece of EVA medium 6
mm thick under IMTPJ (bulked raised shape) covered with a yellow EVA soft layer that was 1 mm
thick.
Figure 2. Typical Morton’s extension orthotic (TMEO).
A flat sheet of ethylene-vinyl acetate (EVA) with a rectangular flat piece of EVA medium 6 mm
thick under IMTPJ covered with a black EVA soft layer that was 1 mm thick.
2.5. Procedure
The podiatric clinician researcher (RSG) performed a physical assessment of the subjects and
applied the eligibility criteria. To visualize the muscle belly, each subject was asked to perform
plantarflexion of the ankle joint for a few seconds. The surface electrodes were then placed
longitudinally onto the most prominent bulge of the gastrocnemius medialis and lateralis, based on
the “European recommendations for surface EMG” [33]. The subjects were then asked to stand on
one leg in the tip-toe position using their dominant foot for 5 s to set the maximal voluntary
contractions that were needed in the strongest limb to calibrate the software and to normalize EMG
data amplitudes for each test [34]. This was followed by acclimatization of subjects to a motorized
treadmill at 5.17 km/h for 3 min [17]. The participants were divided randomly in gastrocnemius
lateralis or medialis group by choosing a sealed envelope that assigned them to one group or
another to begin the test; after that, they selected one of the five sealed envelopes with each of the
five different conditions of the study (SO, NIRO 6 mm, NIRO 8 mm, TMEO 6 mm, TMEO 8 mm) to
set randomly the order of the test. The 11 subjects who began with medialis gastrocnemius
assessments, did the lateralis test following the same randomized protocol for each of the five
different conditions and vice versa for the 12 participants who began with the lateralis test (Figure
3). Three running trials at 9 km/h [35] under five different conditions (SO, NIRO 6 mm, NIRO 8
mm, TMEO 6 mm, and TMEO 8 mm) on the same day were randomly performed. The duration of
each trial was 1 min. For each subject, the mean EMG muscle activity pattern [36] of the
gastrocnemius medialis of the dominant leg was recorded during the last 30 s of each 1-min trial,
which was performed three times, leaving 5 min of rest between each test [37]. To avoid a potential
imbalance, the same condition was added to contralateral foot. The same protocol was performed to
Figure 2. Typical Morton’s extension orthotic (TMEO).
A flat sheet of ethylene-vinyl acetate (EVA) with an inverted rocker piece of EVA medium 6 mm
thick under IMTPJ (bulked raised shape) covered with a yellow EVA soft layer that was 1 mm thick.
A flat sheet of ethylene-vinyl acetate (EVA) with a rectangular flat piece of EVA medium 6 mm
thick under IMTPJ covered with a black EVA soft layer that was 1 mm thick.
2.5. Procedure
The podiatric clinician researcher (RSG) performed a physical assessment of the subjects and
applied the eligibility criteria. To visualize the muscle belly, each subject was asked to perform
plantarflexion of the ankle joint for a few seconds. The surface electrodes were then placed longitudinally
onto the most prominent bulge of the gastrocnemius medialis and lateralis, based on the “European
recommendations for surface EMG” [33]. The subjects were then asked to stand on one leg in the tip-toe
position using their dominant foot for 5 s to set the maximal voluntary contractions that were needed
in the strongest limb to calibrate the software and to normalize EMG data amplitudes for each test [34].
This was followed by acclimatization of subjects to a motorized treadmill at 5.17 km/h for 3 min [17].
The participants were divided randomly in gastrocnemius lateralis or medialis group by choosing a
sealed envelope that assigned them to one group or another to begin the test; after that, they selected
one of the five sealed envelopes with each of the five different conditions of the study (SO, NIRO 6 mm,
NIRO 8 mm, TMEO 6 mm, TMEO 8 mm) to set randomly the order of the test. The 11 subjects who
began with medialis gastrocnemius assessments, did the lateralis test following the same randomized
protocol for each of the five different conditions and vice versa for the 12 participants who began with
the lateralis test (Figure 3). Three running trials at 9 km/h [35] under five different conditions (SO,
NIRO 6 mm, NIRO 8 mm, TMEO 6 mm, and TMEO 8 mm) on the same day were randomly performed.
The duration of each trial was 1 min. For each subject, the mean EMG muscle activity pattern [36] of
the gastrocnemius medialis of the dominant leg was recorded during the last 30 s of each 1-min trial,
which was performed three times, leaving 5 min of rest between each test [37]. To avoid a potential
imbalance, the same condition was added to contralateral foot. The same protocol was performed to
assess another gastrocnemius EMG activity pattern. Subjects were blinded to which of the five random
conditions that they were wearing, and the results were used to test the hypothesis.
Sensors 2020, 20, 3205
5 of 12
Sensors 2020, 20, x FOR PEER REVIEW
5 of 12
assess another gastrocnemius EMG activity pattern. Subjects were blinded to which of the five
random conditions that they were wearing, and the results were used to test the hypothesis.
Figure 3. Randomized flow chart. Abbreviations: SO = shoe only; NIRO = novel inverted rocker
orthoses; and TMEO = traditional Morton extension´s orthoses.
2.6. Statistical Analysis
To test for reliability in the present research, within-day trial-to-trial intraclass correlation
coefficient (ICC) and the standard error of measurement (SEM) were calculated for the subjects
under the five conditions for each muscle during the running test [14]. According to Landis and
Koch [38], coefficients of ICC that were lower than 0.20 indicated a slight agreement, 0.20–0.40
indicated fair reliability, 0.41–0.60 indicated moderate reliability, 0.61–0.80 indicated substantial
reliability, and 0.81–1.00 indicated almost perfect reliability. The authors considered coefficients of
≥0.81 to be appropriate to consider the results of the study as valid. SEM assessed the minimal
detectable change (MDC) for all measurements. This is known as reliable change index (RCI), and it
was used to determine the clinical significance of the data [39]. The Shapiro–Wilks test was used to
assess the normality of the sample, and normal a distribution was present if p >0.05. Demographic
values were presented as the mean and standard deviation (±SD). The p-values for multiple
comparisons were corrected with a non-parametric paired Friedman test to prove that all SOs,
NIROs, and TMEOs conditions were different between them. The Wilcoxon test with Bonferroni’s
correction was performed to analyze differences between the five different conditions, indicating
statistically significant differences when p < 0.05 with a 95% CI. All the values that were generated
using NeuroTrac® software were loaded into Excel® template (Windows® 97–2003), and they were
analyzed using SPSS version 19.0 (SPSS Science, Chicago, IL, USA).
3. Results
The Shapiro–Wilks test showed a non-normal distribution of the sample (p < 0.05), while the
Friedman test showed that values were different between the five conditions (p < 0.05). All subjects
were recruited from a biomechanical clinic in Madrid (Spain) over a two-month period (October to
Figure 3. Randomized flow chart. Abbreviations: SO = shoe only; NIRO = novel inverted rocker
orthoses; and TMEO = traditional Morton extension’s orthoses.
2.6. Statistical Analysis
To test for reliability in the present research, within-day trial-to-trial intraclass correlation coefficient
(ICC) and the standard error of measurement (SEM) were calculated for the subjects under the five
conditions for each muscle during the running test [14]. According to Landis and Koch [38], coefficients
of ICC that were lower than 0.20 indicated a slight agreement, 0.20–0.40 indicated fair reliability,
0.41–0.60 indicated moderate reliability, 0.61–0.80 indicated substantial reliability, and 0.81–1.00
indicated almost perfect reliability. The authors considered coefficients of ≥0.81 to be appropriate to
consider the results of the study as valid. SEM assessed the minimal detectable change (MDC) for
all measurements. This is known as reliable change index (RCI), and it was used to determine the
clinical significance of the data [39]. The Shapiro–Wilks test was used to assess the normality of the
sample, and normal a distribution was present if p >0.05. Demographic values were presented as
the mean and standard deviation (±SD). The p-values for multiple comparisons were corrected with
a non-parametric paired Friedman test to prove that all SOs, NIROs, and TMEOs conditions were
different between them. The Wilcoxon test with Bonferroni’s correction was performed to analyze
differences between the five different conditions, indicating statistically significant differences when
p < 0.05 with a 95% CI. All the values that were generated using NeuroTrac® software were loaded
into Excel® template (Windows® 97–2003), and they were analyzed using SPSS version 19.0 (SPSS
Science, Chicago, IL, USA).
Sensors 2020, 20, 3205
6 of 12
3. Results
The Shapiro–Wilks test showed a non-normal distribution of the sample (p < 0.05), while the
Friedman test showed that values were different between the five conditions (p < 0.05). All subjects
were recruited from a biomechanical clinic in Madrid (Spain) over a two-month period (October to
November 2019). Forty-five subjects were asked to participate in the experiment and assessed for
eligibility; 24 did not meet the study entry requirements and three withdrew from the study because of
pain and discomfort. Ultimately, 21 participants (10 males and 11 females) were enrolled into the study.
The participants’ flow chart following the STROBE guidelines, is shown in Figure 4. Sociodemographic
data are shown in Table 1.
Sensors 2020, 20, x FOR PEER REVIEW
6 of 12
November 2019). Forty-five subjects were asked to participate in the experiment and assessed for
eligibility; 24 did not meet the study entry requirements and three withdrew from the study
because of pain and discomfort. Ultimately, 21 participants (10 males and 11 females) were enrolled
into the study. The participants’ flow chart following the STROBE guidelines, is shown in Figure 4.
Sociodemographic data are shown in Table 1.
Figure 4. Participant flow chart.
Table 1. Participant demographics.
Variable
n = 21
Mean ± SD (95% CI)
Age
31.41 ± 4.33
(32.26–35.09)
FPI (scores)
3.12 ± 0.17
(2.07–3.41)
Weight (kg)
67.50 ± 8.06
(62.36–70.06)
Height (cm)
170.08 ± 6.91
(166.9–172.43)
BMI (kg/m2)
23.15 ± 3.05
(21.7–24.7)
Abbreviations: SD = standard deviation; CI = confidence interval; FPI = foot posture index; and BMI
= body mass index.
The reliability of the data obtained from the EMG activity of muscles during running under
five different conditions is presented as the ICC and SEM, which are shown in Table 2. Most of the
values reached cut-off values over of 0.81 in the ICC data, which suggests “almost perfect
reliability” [38], with 0.971 for NIRO-8 mm as the highest value and 0.458 for TMEO-8 mm as the
lowest for the gastrocnemius lateralis, and 0.894 for TMEO-8 mm as the highest and 0.767 for
NIRO-8 mm as the lowest for the gastrocnemius medialis. Considering the reference that was
chosen by the authors, we dismissed TMEO-8 mm values for gastrocnemius lateralis. For SEM,
0.817 mV was the lowest value set for NIRO-8 mm, and 3.766 mV was the lowest value for TMEO-6
mm for the gastrocnemius lateralis, and 2.083 mV was the highest value for NIRO-8 mm and 0.326
Figure 4. Participant flow chart.
Table 1. Participant demographics.
Variable
n = 21
Mean ± SD (95% CI)
Age
31.41 ± 4.33
(32.26–35.09)
FPI (scores)
3.12 ± 0.17
(2.07–3.41)
Weight (kg)
67.50 ± 8.06
(62.36–70.06)
Height (cm)
170.08 ± 6.91
(166.9–172.43)
BMI (kg/m2)
23.15 ± 3.05
(21.7–24.7)
Abbreviations: SD = standard deviation; CI = confidence interval; FPI = foot posture index; and BMI = body
mass index.
Sensors 2020, 20, 3205
7 of 12
The reliability of the data obtained from the EMG activity of muscles during running under five
different conditions is presented as the ICC and SEM, which are shown in Table 2. Most of the values
reached cut-off values over of 0.81 in the ICC data, which suggests “almost perfect reliability” [38],
with 0.971 for NIRO-8 mm as the highest value and 0.458 for TMEO-8 mm as the lowest for the
gastrocnemius lateralis, and 0.894 for TMEO-8 mm as the highest and 0.767 for NIRO-8 mm as the
lowest for the gastrocnemius medialis. Considering the reference that was chosen by the authors,
we dismissed TMEO-8 mm values for gastrocnemius lateralis. For SEM, 0.817 mV was the lowest
value set for NIRO-8 mm, and 3.766 mV was the lowest value for TMEO-6 mm for the gastrocnemius
lateralis, and 2.083 mV was the highest value for NIRO-8 mm and 0.326 mV was the lowest value for
TMEO-8 mm for the gastrocnemius medialis. The highest MDC value for TMEO-8 mm was 5.798 mV
and 2.264 mV were the lowest value for the gastrocnemius lateralis. Additionally, 5.775 mV was the
highest value in the NIRO-8 mm group and 0.904 mV was the lowest value in the TMEO-8 mm group
for gastrocnemius medialis.
EMG mean muscle activity in the gastrocnemius medialis and lateralis in SO compared to
NIRO-6 mm and 8 mm and TMEO-6 mm and 8 mm are shown in Table 3. In the gastrocnemius
lateralis, the EMG activity significantly increased between the SO and NIRO-8 mm (22.27 ± 2.51
vs. 25.96 ± 4.68 mV; p < 0.05). There was another statistically significant increase between SO and
TMEO-6 mm (22.27 ± 2.51 vs. 24.72 ± 5.08 mV, p < 0.05) and vs. TMEO-8 mm (25.49 ± 1.97, p < 0.001),
but the low ICC of the last value invalidated the reliability of this value. For the gastrocnemius medialis,
a statistically significant increase in the EMG activity was noted for SO vs. NIRO-6 mm (22.93 ± 2.1
vs. 26.44 ± 3.63, p < 0.001), vs. NIRO-8 mm (28.89 ± 3.6, p < 0.001), vs. TMEO-6 mm (25.12 ± 3.51,
p < 0.05), and vs. TMEO-8 mm (26.38 ± 3.02, p < 0.05). The latter was not considered because of its
low ICC value. In addition, the relationship between NIROs and TMEOs showed that there was a
statistically significant increase in NIRO-6 mm and NIRO-8 mm (26.44 ± 3.63 vs. 28.89 ± 3.6, p < 0.05),
and a statistically significant decrease in NIRO-8 mm vs. TMEO-6 mm (28.89 ± 3.6 vs. 25.12 ± 3.51,
p < 0.001) and in NIRO-8 mm vs. TMEO-8 mm (28.89 ± 3.6 vs. 26.38 ± 3.02, p < 0.05), although the
latter could not be considered because of its low ICC values.
Sensors 2020, 20, 3205
8 of 12
Table 2. Reliability ICC of variables with “shoe only” versus 6- and 8-mm of novel inverted rocker orthoses (NIRO) and traditional Morton extension orthoses (TMEO).
Variables
SO
NIRO-6 mm
NIRO-8 mm
TMEO-6 mm
TMEO-8 mm
ICC
(95% CI)
MDC
ICC
(95% CI)
MDC
ICC
(95% CI)
MDC
ICC
(95% CI)
MDC
ICC
(95% CI)
MDC
SEM
0.950
SEM
0.950
SEM
0.950
SEM
0.950
SEM
0.950
Gastrocnemius
lateralis (mV)
0.839
0.932
0.971
0.937
0.458
(0.651–0.935)
1.010
3.560
(0.852–0.973)
1.254
3.477
(0.938–0.988)
0.817
2.264
(0.861–0.975)
1.359
3.766
(0.148–0.777)
2.092
5.798
Gastrocnemius
medialis (mV)
0.848
0.832
0.767
0.872
0.894
(0.649–0.94)
0.913
2.530
(0.637–0.931)
1.707
4.731
(0.501–0.905)
2.083
5.775
(0.723–0.948)
1.408
3.904
(0.77–0.957)
0.326
0.904
Abbreviations: ICC = intraclass correlation coefficient; CI = confidence interval; SEM = standard error of measurement; MDC = minimal detectable change; (mV) = millivolts; SO = shoe
only; and mm = millimeters.
Table 3. Signal amplitudes and comparison values of the mean gastrocnemius lateralis and medialis muscle activities.
SO
NIRO
6 mm
NIRO
8 mm
TMEO
6 mm
TMEO
8 mm
p-Value
SO
p-Value
SO
p-Value
SO
p-Value
SO
p-Value
NIRO
6 mm
p-Value
NIRO
6 mm
p-Value
NIRO
6 mm
p-Value
NIRO 8
mm
p-Value
NIRO
8 mm
p-Value
TMEO
6 mm
Variable
mean (mV)
mean(mV)
mean (mV)
mean (mV)
mean (mV)
vs.
vs.
vs.
vs.
vs.
vs.
vs.
vs.
vs.
vs.
gastrocnemius
lateralis
±SD
(95% CI)
±SD
(95% CI)
±SD
(95% CI)
±SD
(95% CI)
±SD
(95% CI)
NIRO 6
mm
NIRO 8
mm
TMEO 6
mm
TMEO 8
mm
NIRO
8 mm
TMEO
6 mm
TMEO
8 mm
TMEO 6
mm
TMEO
8 mm
TMEO
8 mm
22.27 ± 2.51
24.65 ± 4.51
25.96 ± 4.68
24.72 ± 5.08
25.49 ± 1.97
(20.77–23.279) (22.41–26.897) (23.634–28.29) (23.675–27.35) (22.19–27.253)
0.085
<0.05 *
<0.05 *
<0.001 **
0.39
0.88
0.356
0.372
0.67
0.913
22.93 ± 2.1
26.44 ± 3.63
28.89 ± 3.6
25.12 ± 3.51
26.38 ± 3.02
gastrocnemius
medialis
(21.88–23.97)
(24.63–28.24)
(27–30.68)
(23.37–26.87)
(24.88–27.89)
<0.001 **
<0.001 **
<0.05 *
<0.05 *
<0.05 *
0.06
0.67
<0.001 **
<0.05 *
0.22
Abbreviations: mV = millivolts; SO = shoe only; NIRO = novel inverted rocker orthoses; TMEO = traditional Morton extension orthoses; mm = millimeters; ±SD = standard deviation;
p < 0.05 * (95% CI) was considered statistically significant; and p < 0.001 ** (95% CI) was considered statistically significant.
Sensors 2020, 20, 3205
9 of 12
4. Discussion
4.1. TMEO and NIRO Effects
This is the first study on EMG muscle activity in the gastrocnemius medialis and lateralis under
IMTPJ dorsiflexion mobility restrictions by two different kinds of orthoses, the TMEO and the NIRO,
in healthy subjects during running. TMEO has been used to treat symptoms of the first stages of
OA [9–11] moving away dorsally from the contact between the proximal phalanx of the hallux and first
metatarsal head surfaces. However, it is unclear if the effects on the triceps surae activity that were
caused by the windlass mechanism [24] alteration through the IMTPJ caused the restriction. Some
authors have shown the need for proper dorsiflexion of the IMTPJ during the push-off phase to ensure
normal activity of the calcaneus–plantar system [24]. We hypothesized that TMEO would increase the
EMG triceps surae activity that is induced by restriction of IMTPJ dorsiflexion. Our results showed
that EMG activity of the gastrocnemius lateralis and medialis increased with TMEO-6 mm and that
there is a further increase with TMEO-8 mm compared to SO (Table 3), although the last one could
not be considered because of the low ICC values. Even knowing that there are no studies related to
EMG activity during running with the orthopedic restriction of IMPTJ dorsiflexion, these results are
consistent with other simulated running research [24,25], which showed that engaging the windlass
mechanism by promoting 30◦ of IMTPJ dorsiflexion caused the arch to absorb and dissipate more
elastic energy than under normal circumstances, and likely the energy of the triceps surae would be
saved. In the present research, we decreased the windlass capacity through the TMEO, and followed
the lack of storage and release energy in the medial longitudinal arch primary in the heel-off phase;
this could have been supported by increasing gastrocnemius musculature EMG activity, as shown
by our results, and by sustaining the connection between the IMTPJ and triceps surae through the
windlass mechanism, according with other authors [24,25].
We hypothesized that NIRO would produce less EMG activity on triceps surae than the TMEO
compared to SO. The rationale behind this approach was that its smooth edges and inverted rocker
would produce a slight movement restriction of the IMTPJ; therefore, less effort would be required of
the triceps surae to move the heel up. However, the present research showed surprising results, with a
higher increase in EMG activity in both the gastrocnemius medialis and lateralis muscles (Table 3) with
NIRO compared to TMEO, especially with NIRO-8 mm. This could be partly explained because of
the soft edges of the NIRO, which yielded instability on the IMTPJ and transferred it to triceps surae
in the heel-off phase. This is consistent with other studies with inverted rocker-sole shoes [40] that
showed increased plantarflexion at the ankle joint and an increase in lower limb muscular activity [13].
This conclusion is not consistent with other research that showed increasing toe joint stiffness and
increased ankle foot push-off work by up to 181% [41].
4.2. Osteoarthritis
OA has been defined as one of the most important and incapacitating musculoskeletal disorders in
the world and OA of the IMTPJ, is the most commonly affected region on the foot [42]. This pathology
can involves partial (FHL) or total (HR) rolling fail of the proximal phalanx of the hallux around first
metatarsal bone in the last phase of gait [3], and there are a few treatments to relieve them, looking to
avoid contact of the dorsal aspect of theses bones, such as TMEO [9–11] or classical rocker soles [12].
No studies about triceps surae EMG activity and IMTPJ OA using orthoses and/or rocker soles during
running have been reported; nevertheless, our observations with simulated IMTPJ restriction through
TMEO and NIRO, showed an increase of EMG activity pattern of the gastrocnemius medialis and
lateralis, in contrast with a recently study [12] with IMTPJ OA and traditional rocker bottom soles,
which argued that the reduction of the concentric activity of the triceps surae inferred from the forward
displacements of the body center of mass was probably due to passively roll-over of the whole base
of support.
Sensors 2020, 20, 3205
10 of 12
4.3. Running Economy
Elastic energy is stored and returned by the plantar muscles, plantar aponeurosis, and triceps
surae with the Achilles tendon during the mid-stance and heel-off phases of running because of its
isometric, concentric, and eccentric stretching–shortening pattern [43,44], which shows that the foot
has an important role in RE. RE is related to different biomechanical parameters such as shorter ground
contact times, higher stride frequency, joint stiffness, and neuromuscular response [20], specifically
the pre-activation of gastrocnemius muscular group [14,17,20]. TMEO and NIRO somehow produced
decreased stiffness in the IMTPJ by dorsal migration of the I metatarsal bone, and this was shown by the
compensatory increase effect on the gastrocnemius musculature activity that attempts to stabilize IMTPJ
instability when joined with the windlass mechanism. This would cause worse RE [20]. Our obtained
values confirm the results of some studies [45,46], which showed the importance of neuromuscular
pre-activation of the gastrocnemius to increase the leg stiffness, anticipating the loading forces and
attenuating the effort of the foot to stabilize the joint as required, improving the energy cost and,
therefore, the RE.
5. Limitations
The sample size that was calculated in a previous study could not be attained because three
individuals were excluded. This must be taken into account when interpreting the results. In addition,
we were not able to assess the “order effect” on our sample because didn’t write the different orders
of each participant’s choice, despite the fact that both groups had a similar participant number,
the hypothetical order effect can take over, and we recommended future study designed to improve
this aspect of the assessments.
Because of the short running test duration when NIRO and TMEO were worn, the hypothetical
muscular adaptations of the triceps surae could not be assessed. Longer studies in the future are
needed to determine how the exertion levels can influence these muscular adaptations during running.
Considering that most ±SD values obtained in the present research are higher than SEM, authors
recommended to have caution in interpreting the results.
6. Conclusions
NIRO and TMEO have shown a high interaction with triceps surae, increasing the gastrocnemius
medialis and lateralis EMG activity during running.
This may be additional evidence of the
biomechanics relationship between IMTPJ and the windlass mechanism connection. Higher values
of the triceps surae EMG activity wearing NIRO and TMEO during running could have a negative
impact on RE; therefore, clinicians should be prescribing them with caution when they want to treat
IMTPJ OA in runners.
Author Contributions: Conceptualization, R.S.-G.; methodology, C.R.-M., M.K. and I.O.-S.; software, I.Z.-G. and
I.O.-S.; validation, Á.G.-C. and P.A.; formal analysis, C.R.-M., B.D.-l.-C.-T. and I.Z.-G.; investigation, R.S.-G. and
P.A.; resources, C.R.-M. and B.D.-l.-C.-T.; data curation, B.D.-l.-C.-T.; writing—original draft preparation; R.S.-G.,
C.R.-M., B.D.-l.-C.-T., I.O.-S., I.Z.-G., P.A. and M.K.; visualization, P.A.; supervision, Á.G.-C. and M.K.; project
administration, B.D.-l.-C.-T. All authors have read and agreed to the published version of the manuscript
Funding: This research received no external fundings.
Conflicts of Interest: The authors declare no conflict of interest.
References
1.
Cotterill, J.M. Stiffness of the Great Toe in Adolescents. Br. Med. J. 1887, 1, 1158. Available online:
http://www.ncbi.nlm.nih.gov/pubmed/20751923 (accessed on 21 February 2019). [CrossRef] [PubMed]
2.
Laird, P.O. Functional Hallux Limitus. Ill. Podiatr. 1972, 9, 4.
3.
Drago, J.J.; Oloff, L.; Jacobs, A.M. A comprehensive review of hallux limitus. J. Foot Surg. 1984, 23, 213–220.
[PubMed]
Sensors 2020, 20, 3205
11 of 12
4.
Zammit, G.V.; Menz, H.B.; Munteanu, S.E. Structural factors associated with hallux limitus/rigidus:
A systematic review of case control studies. J. Orthop. Sports Phys. Ther. 2009, 39, 733–742. [CrossRef]
[PubMed]
5.
Dananberg, H.J. Functional hallux limitus and its relationship to gait efficiency. J. Am. Podiatr. Med.
Assoc. 1986, 76, 648–652. Available online: http://www.ncbi.nlm.nih.gov/pubmed/3814239 (accessed on
17 August 2015). [CrossRef]
6.
Tenforde, A.S.; Yin, A.; Hunt, K.J. Foot and Ankle Injuries in Runners. Physical Medicine and Rehabilitation
Clinics of North America; Saunders, W.B., Ed.; Elsevier Inc.: Amsterdam, The Netherlands, 2016; Volume 27,
pp. 121–137. Available online: http://www.ncbi.nlm.nih.gov/pubmed/26616180 (accessed on 15 May 2020).
7.
Polzer, H.; Polzer, S.; Brumann, M.; Mutschler, W.; Regauer, M. Hallux rigidus: Joint preserving alternatives
to arthrodesis—A review of the literature. World J. Orthop. 2014, 5, 6–13. [CrossRef]
8.
Shurnas, P.S. Hallux Rigidus: Etiology, Biomechanics, and Nonoperative Treatment. Foot Ankle Clin. 2009,
14, 1–8. [CrossRef]
9.
Dananberg, H.J. Gait style as an etiology to chronic postural pain. Part, I. Functional hallux limitus. J. Am.
Podiatr. Med. Assoc. 1993, 83, 433–441. [CrossRef]
10.
Smith, R.W.; Katchis, S.D.; Ayson, L.C. Outcomes in hallux rigidus patients treated nonoperatively:
A long-term follow-up study. Foot Ankle Int. 2000, 21, 906–913. [CrossRef]
11.
Grady, J.F.; Axe, T.M.; Zager, E.J.; Sheldon, L.A. A retrospective analysis of 772 patients with hallux limitus.
J. Am. Podiatr. Med. Assoc. 2002, 92, 102–108. [CrossRef]
12.
Menz, H.B.; Auhl, M.; Tan, J.M.; Levinger, P.; Roddy, E.; Munteanu, S.E. Biomechanical Effects of Prefabricated
Foot Orthoses and Rocker-Sole Footwear in Individuals with First Metatarsophalangeal Joint Osteoarthritis.
Arthritis Care Res. 2016, 68, 603–611. [CrossRef]
13.
Romkes, J.; Rudmann, C.; Brunner, R. Changes in gait and EMG when walking with the Masai Barefoot
Technique. Clin. Biomech. 2006, 21, 75–81. Available online: https://www.sciencedirect.com/science/article/
abs/pii/S0268003305001816 (accessed on 15 May 2020). [CrossRef] [PubMed]
14.
Saunders, P.U.; Pyne, D.B.; Telford, R.D.; Hawley, J.A. Reliability and variability of running economy in elite
distance runners. Med. Sci. Sports Exerc. 2004, 36, 1972–1976. [CrossRef] [PubMed]
15.
Hayes, P.R.; Bowen, S.J.; Davies, E.J. The relationships between local muscular endurance and kinematic
changes during a run to exhaustion at vVO2MAX. J. Strength Cond. Res. 2004, 18, 898–903.
16.
Roca-Dols, A.; Losa-Iglesias, M.E.; Sánchez-Gómez, R.; Becerro-de-Bengoa-Vallejo, R.; López-López, D.;
Rodríguez-Sanz, D.; Martínez-Jiménez, E.M.; Calvo-Lobo, C. Effect of the cushioning running shoes in
ground contact time of phases of gait. J. Mech. Behav. Biomed. Mater. 2018, 88, 196–200. [CrossRef] [PubMed]
17.
Roca-Dols, A.; Elena Losa-Iglesias, M.; Sánchez-Gómez, R.; Becerro-de-Bengoa-Vallejo, R.; López-López, D.;
Palomo-López, P.; Rodríguez-Sanz, D.; Calvo-Lobo, C. Electromyography activity of triceps surae and tibialis
anterior muscles related to various sports shoes. J. Mech. Behav. Biomed. Mater. 2018, 86, 158–171. [CrossRef]
18.
Roca-Dols, A.; Losa-Iglesias, M.E.; Sánchez-Gómez, R.; López-López, D.; Becerro-de-Bengoa-Vallejo, R.;
Calvo-Lobo, C. Electromyography comparison of the effects of various footwear in the activity patterns of
the peroneus longus and brevis muscles. J. Mech. Behav. Biomed. Mater. 2018, 82, 126–132. [CrossRef]
19.
Blagrove, R.C.; Howatson, G.; Hayes, P.R. Effects of Strength Training on the Physiological Determinants of
Middle- and Long-Distance Running Performance: A Systematic Review. Sports Medicine; Springer International
Publishing: Cham, Switzerland, 2018; Volume 48, pp. 1117–1149.
20.
Tam, N.; Tucker, R.; Santos-Concejero, J.; Prins, D.; Lamberts, R.P. Running Economy: Neuromuscular and
Joint-Stiffness Contributions in Trained Runners. Int. J. Sports Physiol. Perform. 2019, 14, 16–22. [CrossRef]
21.
Hicks, J. The mechanics of the foot. II. The plantar aponeurosis and the arch. J. Anat. 1954, 88, 25–30.
22.
Stearne, S.M.; McDonald, K.A.; Alderson, J.A.; North, I.; Oxnard, C.E.; Rubenson, J. The Foot’s Arch and the
Energetics of Human Locomotion. Sci. Rep. 2016, 6, 1–10. [CrossRef]
23.
Ker, R.F.; Bennett, M.B.; Bibby, S.R.; Kester, R.C.; Alexander, R.M. The spring in the arch of the human foot.
Nature 1987, 325, 147–149. [CrossRef]
24.
Maceira, E.; Monteagudo, M. Functional hallux rigidus and the Achilles-calcaneus-plantar system. Foot Ankle
Clin. 2014, 19, 669–699. [CrossRef]
25.
Welte, L.; Kelly, L.A.; Lichtwark, G.A.; Rainbow, M.J. Influence of the windlass mechanism on arch-spring
mechanics during dynamic foot arch deformation. J. R. Soc. Interface 2018, 15, 20180270. [CrossRef]
Sensors 2020, 20, 3205
12 of 12
26.
Johanson, M.A.; Allen, J.C.; Matsumoto, M.; Ueda, Y.; Wilcher, K.M. Effect of Heel Lifts on Plantarflexor and
Dorsiflexor Activity During Gait. Foot Ankle Int. 2010, 31, 1014–1020. [CrossRef] [PubMed]
27.
Von Elm, E.; Altman, D.G.; Egger, M.; Pocock, S.J.; Gøtzsche, P.C.; Vandenbroucke, J.P. The Strengthening
the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for reporting
observational studies. Int. J. Surg. 2014, 12, 1495–1499. [CrossRef] [PubMed]
28.
Redmond, A.C.; Crosbie, J.; Ouvrier, R.A. Development and validation of a novel rating system for scoring
standing foot posture: The Foot Posture Index. Clin. Biomech. (Bristol. Avon.) 2006, 21, 89–98. [CrossRef]
29.
Root, M.L.; Orien, W.P.; Weed, J.H.; Hughes, R.J. Normal and Abnormal Function of the Foot; Clinical
Biomechanics Corp.: Los Angeles, CA, USA, 1977; Volume 2.
30.
Sánchez-Gómez, R.; Becerro-de-Bengoa-Vallejo, R.; Losa-Iglesias, M.E.; Calvo-Lobo, C.; Navarro-Flores, E.;
Palomo-López, P.; Romero-Morales, C.; López-López, D. Reliability Study of Diagnostic Tests for Functional
Hallux Limitus. Foot Ankle Int. 2020, 41, 457–462. [CrossRef] [PubMed]
31.
Garrow, J.S.; Webster, J. Quetelet’s index (W/H2) as a measure of fatness. Int. J. Obes. 1985, 9, 147–153.
[PubMed]
32.
Naess, I.; Bø, K. Can maximal voluntary pelvic floor muscle contraction reduce vaginal resting pressure and
resting EMG activity? Int. Urogynecol. J. 2018, 29, 1623–1627. [CrossRef]
33.
Hermens, H.J.; Freriks, B.; Disselhorst-Klug, C.; Rau, G. Development of recommendations for SEMG sensors
and sensor placement procedures. J. Electromyogr. Kinesiol. 2000, 10, 361–374. [CrossRef]
34.
Murley, G.S.; Buldt, A.K.; Trump, P.J.; Wickham, J.B. Tibialis posterior EMG activity during barefoot walking
in people with neutral foot posture. J. Electromyogr. Kinesiol. 2009, 19, e69–e77. [CrossRef] [PubMed]
35.
Shih, Y.; Lin., K.-L.; Shiang, T.-Y. Is the foot striking pattern more important than barefoot or shod conditions
in running? Gait Posture 2013, 38, 490–494. [CrossRef] [PubMed]
36.
Goto, K.; Abe, K. Gait characteristics in women’s safety shoes. Appl. Ergon. 2017, 65, 163–167. [CrossRef]
37.
Fleming, N.; Walters, J.; Grounds, J.; Fife, L.; Finch, A. Acute response to barefoot running in habitually shod
males. Hum. Mov. Sci. 2015, 42, 27–37. [CrossRef] [PubMed]
38.
Landis, J.R.; Koch, G.G. The measurement of observer agreement for categorical data. Biometrics 1977, 33,
159–174. [CrossRef] [PubMed]
39.
Jacobson, N.; Truax, P. Clinical significance: A statistical approach to defining meaningful change in
psychotherapy research. J. Consult Clin. Psychol. 1991, 59, 12–19. [CrossRef]
40.
Myers, K.A.; Long, J.T.; Klein, J.P.; Wertsch, J.J.; Janisse, D.; Harris, G.F. Biomechanical implications of the
negative heel rocker sole shoe: Gait kinematics and kinetics. Gait Posture 2006, 24, 323–330. [CrossRef]
41.
Honert, E.C.; Bastas, G.; Zelik, K.E. Effect of toe joint stiffness and toe shape on walking biomechanics.
Bioinspir. Biomim. 2018, 13, 066007. [CrossRef]
42.
Sebbag, E.; Felten, R.; Sagez, F.; Sibilia, J.; Devilliers, H.; Arnaud, L. The world-wide burden of musculoskeletal
diseases: A systematic analysis of the World Health Organization Burden of Diseases Database. Ann. Rheum.
Dis. 2019, 78, 844–848. [CrossRef]
43.
Biewener, A.A.; Roberts, T.J. Muscle and tendon contributions to force, work, and elastic energy savings:
A comparative perspective. Exerc. Sport Sci. Rev. 2000, 28, 99–107.
44.
Wilson, A.; Lichtwark, G. The anatomical arrangement of muscle and tendon enhances limb versatility and
locomotor performance. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2011, 366, 1540–1553. [CrossRef] [PubMed]
45.
Boyer, K.A.; Nigg, B.M. Muscle activity in the leg is tuned in response to impact force characteristics.
J. Biomech. 2004, 37, 1583–1588. [CrossRef] [PubMed]
46.
Hamner, S.R.; Seth, A.; Delp, S.L. Muscle contributions to propulsion and support during running. J. Biomech.
2010, 43, 2709–2716. [CrossRef] [PubMed]
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).
(...TRUNCATED) | Effects of Novel Inverted Rocker Orthoses for First Metatarsophalangeal Joint on Gastrocnemius Muscle Electromyographic Activity during Running: A Cross-Sectional Pilot Study.(...TRUNCATED) | 06-05-2020 | Sánchez-Gómez, Rubén,Romero-Morales, Carlos,Gómez-Carrión, Álvaro,De-la-Cruz-Torres, Blanca,Zaragoza-García, Ignacio,Anttila, Pekka,Kantola, Matti,Ortuño-Soriano, Ismael(...TRUNCATED) | eng |
PMC7379642 | "Supplement Table 7. Change in VO2max (L·min-1 and ml·min-1·kg-1) from 1995-1997 to 2016-2017 in (...TRUNCATED) | Decline in cardiorespiratory fitness in the Swedish working force between 1995 and 2017.(...TRUNCATED) | 11-15-2018 | "Ekblom-Bak, Elin,Ekblom, Örjan,Andersson, Gunnar,Wallin, Peter,Söderling, Jonas,Hemmingsson, Erik(...TRUNCATED) | eng |
PMC6358870 | "medicina\nArticle\nPacing of Women and Men in Half-Marathon\nand Marathon Races\nPantelis T. Nikola(...TRUNCATED) | Pacing of Women and Men in Half-Marathon and Marathon Races.(...TRUNCATED) | 01-14-2019 | Nikolaidis, Pantelis T,Ćuk, Ivan,Knechtle, Beat(...TRUNCATED) | eng |
PMC6720831 | "International Journal of\nEnvironmental Research\nand Public Health\nArticle\nBlood Lactate Conce(...TRUNCATED) | "Blood Lactate Concentration Is Not Related to the Increase in Cardiorespiratory Fitness Induced by (...TRUNCATED) | 08-09-2019 | "Astorino, Todd A,DeRevere, Jamie L,Anderson, Theodore,Kellogg, Erin,Holstrom, Patrick,Ring, Sebasti(...TRUNCATED) | eng |
End of preview. Expand
in Dataset Viewer.
- Downloads last month
- 54