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International Journal of
Environmental Research
and Public Health
Article
Daily Resting Heart Rate Variability in Adolescent
Swimmers during 11 Weeks of Training
Sigitas Kamandulis 1, Antanas Juodsnukis 1, Jurate Stanislovaitiene 1, Ilona Judita Zuoziene 1,
Andrius Bogdelis 1, Mantas Mickevicius 1, Nerijus Eimantas 1, Audrius Snieckus 1, *,
Bjørn Harald Olstad 2and Tomas Venckunas 1
1Institute of Sports Science and Innovation, Lithuanian Sports University, 44221 Kaunas, Lithuania;
sigitas.kamandulis@lsu.lt (S.K.); antanas.juodsnukis@lsu.lt (A.J.); jurate.stanislovaitiene@lsu.lt (J.S.);
ilona.zuoziene@lsu.lt (I.J.Z.); andrius.bogdelis@gmail.com (A.B.); mantas.mickevicius@lsu.lt (M.M.);
nerijus.eimantas@lsu.lt (N.E.); tomas.venckunas@lsu.lt (T.V.)
2Institute of Physical Performance, Norwegian School of Sport Sciences, 0863 Oslo, Norway;
b.h.olstad@nih.no
*Correspondence: audrius.snieckus@lsu.lt; Tel.: +370-37-302-621
Received: 5 March 2020; Accepted: 20 March 2020; Published: 22 March 2020
Abstract:
Adolescent athletes are particularly vulnerable to stress. The current study aimed to
monitor one of the most popular and accessible stress markers, heart rate variability (HRV), and its
associations with training load and sleep duration in young swimmers during an 11-week training
period to evaluate its relevance as a tool for monitoring overtraining. National-level swimmers
(n =22, age 14.3
±
1.0 years) of sprint and middle distance events followed individually structured
training programs prescribed by their swimming coach with the main intention of preparing for the
national championships. HRV after awakening, during sleep and training were recorded daily. There
was a consistent ~4.5% reduction in HRV after 3–5 consecutive days of high (>6 km/day) swimming
volume, and an inverse relationship of HRV with large (>7.0 km/day) shifts in total training load
(r =
−
0.35, p<0.05). Day-to-day HRV did not significantly correlate with training volume or sleep
duration. Taken together, these findings suggest that the value of HRV fluctuations in estimating the
balance between the magnitude of a young athlete’s physical load and their tolerance is limited on
a day-to-day basis, while under sharply increased or extended training load the lower HRV becomes
an important indicator of potential overtraining.
Keywords:
autonomic nervous system; competitive swimming; high-intensity exercise; sleep;
training volume
1. Introduction
For training to be effective, it is essential to have both appropriate planning and to implement
a training load monitoring and adjustment system that includes biofeedback [
1
]. Sport practitioners
are constantly looking for ways to most objectively, quickly, and cost-effectively design individualized
training programs. Such programs are based on the individual adaptation, as reflected by the
recuperation (restitution) and super-compensation of the body functions during the recovery period
after training sessions, to maximize long-term gains in performance while at the same time avoiding
excessive fatigue, overtraining and injuries. For a successful design of such programs, it is important
to use integrated training monitoring tools that allow recording variables representing changes in
whole-body functional state, rather than fluctuations of very specific/isolated markers. One marker of
the functional status of an organism, that gives an indication of the balance between the sympathetic
and parasympathetic nervous system, is heart rate variability (HRV). This indicator has recently
Int. J. Environ. Res. Public Health 2020,17, 2097; doi:10.3390/ijerph17062097 www.mdpi.com/journal/ijerph
Int. J. Environ. Res. Public Health 2020,17, 2097 2 of 12
become quite popular and has been associated with numerous conditions ranging from sleep quality
to sports performance [2–6].
HRV represents fluctuations in electrocardiogram (ECG) R–R time interval and reflects cardiac
regulation by the autonomic nervous system based on the instantaneous sum effects of sympathetic and
parasympathetic systems in response to both physical and psychological stimuli [
7
]. Exercise activates
the sympathetic nervous system, causing an increase in myocardial contractility and vasoconstriction
of peripheral blood vessels, which are moderated by the parasympathetic nervous system [
8
,
9
]. Recent
reviews suggest that HRV biofeedback is a method that is effective and safe, and is easy to learn
and apply to improve sport performance [
4
,
8
]. It has also been highlighted that HRV may reflect the
training-induced level of stress and recovery, which has encouraged regular HRV monitoring [
3
,
10
].
However, it has also been shown that overload training leading to overreaching has little effect on
resting HRV or increased postexercise HRV, and that day-to-day load variability was not related to
HRV (for review, see Bellinger et al., [
3
]). Thus, although HRV has been investigated extensively, its
practical use in everyday training remains controversial [2,3].
Handling individual training-induced responses is particularly relevant in such sports as
swimming, where the risk of overreaching and overtraining is high because of the very large
volume and monotonous training loads and early specialization by athletes [
11
]. As reviewed by
Koenig et al. [
12
], although HRV monitoring in swimming may have some beneficial outcomes, it is
also recognized that there is a lack of translational approaches to apply the current evidence to general
practice. Several recent studies demonstrated the relationships between the autonomic nervous system,
performance, and fatigue, showing that HRV responses appeared to depend on the training status,
age, and environmental factors of the athletes [
13
–
17
]. However, the vastly different populations and
contexts of these studies create uncertainty about the interpretation of their findings, which may partly
explain why sport practitioners are still reluctant to incorporate HRV monitoring into their arsenal of
training tools.
Because of the above considerations, we feel that the utility of HRV as a training load monitoring
tool requires further examination in young competitive swimmers. Adolescents were selected for
the investigation because they may be particularly vulnerable to overreaching because of their
structural, biomechanical, and, consequently, functional alterations related to the intrinsic effects
of rapid somatic growth and development [
18
,
19
]. Adolescence is also associated with increased
sensitivity to environmental conditions (stress related to school activities, relationships with parents,
friends, etc.) and therefore it is particularly important to control stress and recovery in competitive
athletes of this age. Better understanding of training-specific HRV responses may optimize athletic
activity and prevent the development of long-lasting fatigue. The main aim of this study was therefore
to analyze HRV associations with training load and sleep duration during the 11-week training
macrocycle of young swimmers. We hypothesized that HRV measurements would be feasible during
the preparatory training period of young swimmers, that total training volume and high-intensity (HI)
training volume would be inversely correlated with HRV, and that sleep duration would be directly
correlated with HRV.
2. Materials and Methods
2.1. Participants
Twenty-five adolescent swimmers at national level from the same swimming school were initially
recruited to the study. The inclusion criteria were: (1) healthy, (2) absence of any clinical history of
neuromuscular disorders within preceding year, (3) regular swimming training of at least 5 years;
(4) competitive at least at national level, and (5) early or middle adolescence (13–16 years). However,
three athletes were excluded because of inconsistent R–R interval measurements. The characteristics
of the participants for whom data were analyzed (n =22) are shown in Table 1. Athletes were
following periodized training programs that were individually developed and prescribed by their
Int. J. Environ. Res. Public Health 2020,17, 2097 3 of 12
swimming coach with the main intention of preparing them for the national swimming championships.
This period of training had been preceded by a nonathletic period of passive rest during the summer
holiday and a transition period from rest to regular training that comprised light training 4–5 times per
week for two weeks. A standard training week comprised 5–7 swimming sessions, most of which
were held in the afternoons on Mondays to Fridays (the days they all attended lessons in the school
during the morning hours), and some sessions in the mornings during the week. Just before each
afternoon swimming session, participants performed dry-land mobility and strength exercises of
30–45 min in duration. Training required a minimum of 8 hours per week. There was a substantial
variation in training compliance (76.0
±
17.2%), but the athletes with low compliance (two below
50%) were not excluded from the analyses because load variability was considered as a factor in HRV.
Swimmers specialized in events of different strokes at short to middle distances and had at least 5 years
of swimming training experience. All participants and their parents signed an informed consent form
prior to participation. The study was approved by the relevant bioethics committee of the Lithuanian
Sports University (No. BEK-KIN(B)-2019-184). The study was conducted in accordance with the
Declaration of Helsinki.
Table 1. Characteristics of the participants (mean and standard deviation).
Variable Male (n =7) Female (n =15) Total (n =22)
Age, years 15.4 (0.7) 13.8 (0.6) ˆ 14.3 (1.0)
Height, cm 179.5 (6.0) 165.1 (6.7) ˆ 169.7 (9.3)
Weight, kg 65.5 (6.7) 56.5 (6.1) ˆ 59.4 (7.5)
Body fat, % 10.8 (3.9) 21.5 (3.8) ˆ 18.1 (6.3)
Knee extension peak torque, Nm/s
197.3 (20.7) 141.4 (27.5) ˆ 159.2 (36.6)
Vertical jump height, cm 40.2 (2.1) 31.2 (3.3) ˆ 33.8 (5.1)
VO2peak, mL/min/kg 47.8 (5.0) 38.8 (6.8) ˆ 41.6 (7.5)
Maturity
Tanner II, n (%) 1 (14.3 %) 2 (13.3 %) 3 (13.6 %)
Tanner III, n (%) 5 (71.4 %) 11 (73.4 %) 16 (72.8 %)
Tanner IV, n (%) 1 (14.3 %) 2 (13.3 %) 3 (13.6 %)
Note: ˆ p<0.05 vs. male.
2.2. Study Design
The swimmers were followed for 77 days of the preseason training period (September to November)
of which 11 days were preplanned to be without training sessions. HRV and sleep duration were
measured daily by the athletes themselves. The intensity and volume of the training load of each
swimmer were recorded daily by the swimming coaches in the athlete’s training log and then provided
to the researchers. The training loads were not adjusted or corrected as a result of the data collected in
the framework of the current study, and decisions to select training loads, modalities, intensities etc.,
were completely at the discretion of the athletes’ coaches. During the period of the study, the swimmers
took part in 2–3 local competitions. One week before the experimental period, participants were
familiarized with the use and proper fitting of heart rate and sleep monitoring devices, their somatic
maturational status was verified by experienced medical staffusing the Tanner scale [
20
]. We evaluated
participants’ body height (Anthropometry Martin, GPM Siber-Hegner, Geneva, Switzerland), body
weight and fat percentage (Tanita, model TBF 300; Tokyo, Japan), jump height (Power Timer Testing
System, Newest, Finland), dominant leg knee extension strength at angular speed 30
◦·
s
−1
(System 3;
Biodex Medical Systems, Shirley, NY, USA), and VO
2peak
on a stationary cycling ergometer (Ergoline,
Windhagen, Germany) using a portable breath-by-breath analyzer (Oxygen Mobile; Jaeger/VIASYS
Healthcare, Hoechberg, Germany).
Int. J. Environ. Res. Public Health 2020,17, 2097 4 of 12
2.3. Training Load Monitoring
The specific swimming training was performed in a 25-m standard swimming pool and was
stratified according to heart rate (HR) into intensity zones 1 to 4: <139 beats/min (bpm) for Zone 1,
150
±
10 bpm for Zone 2, 170
±
10 bpm for Zone 3, and >181 bpm for Zone 4; sprints with maximal
exertion level were classified as Zone 5. The intensity control was based on criterion speed individually
directed by coach in conjunction with pulse count using a chronometer “Alpha” (Sport-Thieme,
Grasleben, Germany) for 15 s after distinct swimming tasks. All swimmers were experienced in
manually measuring pulse. Swimming at Zones 4 and 5 was considered HI training. Total swimming
volume and HI swimming volume were analyzed as distance covered during the training period.
2.4. HRV Measurement
Over the 11 consecutive weeks of their preparatory training period, swimmers daily measured
their HRV in the supine position for 2 min immediately after awakening in the morning by positioning
an H10 Bluetooth HR strap (Polar Electro, Kempele, Finland) paired with a freely available smartphone
application (Elite HRV, Ashville, NC, USA) on their chest. This system has been used previously
for daily measurement of HRV [
21
]. We analyzed the square root of the mean sum of the squared
differences between R–R intervals (RMSSD), which was converted by logarithmic transformation
(lnRMSSD) to avoid outliers and simplify the analyses, as suggested by Nakamura et al. [
22
]. Data
files were visually inspected for artefacts, and corrections made manually if necessary. Both RMSSD
and lnRMSSD are recognized markers of parasympathetic activity and are the preferred HRV markers
for field-based monitoring [2].
2.5. Sleep Monitoring
During the study, all participants slept in their homes and went to bed at around 11 pm. Participants
wore an activity monitoring bracelet on the wrist of their nondominant hand every night. Daily sleep
duration was monitored by a commercially available wrist-worn sleep/activity tracker, Mi band 2 [
23
].
Moderate intraclass correlation coefficients (ICC) of 0.62–0.75 have been reported for the Mi Band 2
sleep duration assessment [24].
2.6. Statistical Analyses
All variables are expressed in terms of mean
±
standard deviation (SD). Levene’s test was used to
test the homogeneity of variances. The Kolmogorov–Smirnov test was used for checking distribution
normality. A one-way analysis of variance (ANOVA) was used to determine the effects of time on
dependent values (load, HI load, sleep, RMSSD and lmRMSSD) across weeks or days during the
training period. If a significant main effect was found, the significance of the difference between means
was estimated by applying paired t-tests. Statistical power (observed power, OP) was calculated and
presented where appropriate. During the monitoring period, there were 23 cases when individual
swimmers had 3–5 consecutive days of high total training volume (>6 km/day), and 24 cases of 3–5
consecutive days of passive rest not related to injuries or illnesses (on several occasions for some
individuals). These cases were analyzed separately by comparing HRV at the beginning and end of
each period using paired t-tests. An independent t-test was used for comparisons of baseline values
between females and males. The level of significance was set at 5% (p<0.05). Pearson’s correlation (r)
was used to quantify the relationship between each daily RMSSD or lnRMSSD and the previous day’s
training variables. The correlation was considered strong if r>0.5; moderate if r=0.3–0.5; and weak if
r=0.1–0.3 [
25
]. All data analyses were performed using IBM SPSS Statistics software (v.22; IBM Corp.,
Armonk, NY, USA).
Int. J. Environ. Res. Public Health 2020,17, 2097 5 of 12
3. Results
Body weight, height, and dry-land performance were higher in males than in females and fat
percentage was lower in males than in females (both p<0.05) (Table 1). Because HRV and maturation
level were not gender dependent, all the data were pooled for the analysis.
3.1. Training Volume
Total swimming training volume was 232.1
±
81.7 km during the 11 weeks, with training at HI
(combined zones 4 and 5) comprising 6.7
±
4% of total swimming volume. There was a significant
week-by-week variation in total swimming volume, with the highest peak at week 6 (>6.0 km/per day,
p<0.05, OP =0.99) (Figure 1). Peaks of the swimming volume that reached HI zones were evident
in weeks 4, 8, and 9 (about 0.5 km/per day, p<0.05, OP =0.65). Total training volume was reduced
on Wednesdays (p<0.05 compared with Mondays and Tuesdays, OP =0.95) and Saturdays (p<0.05
compared with any other day, OP =0.99), with usually no load on Sundays. HI swimming volume did
not vary significantly between days within a week.
Int. J. Environ. Res. Public Health 2020, 17, x FOR PEER REVIEW 5 of 12
day, p < 0.05, OP = 0.99) (Figure 1). Peaks of the swimming volume that reached HI zones were
evident in weeks 4, 8, and 9 (about 0.5 km/per day, p < 0.05, OP = 0.65). Total training volume was
reduced on Wednesdays (p < 0.05 compared with Mondays and Tuesdays, OP = 0.95) and Saturdays
(p < 0.05 compared with any other day, OP = 0.99), with usually no load on Sundays. HI swimming
volume did not vary significantly between days within a week.
Figure 1. Total (a, b) and high-intensity (c, d) training volume, sleep (e, f) and lnRMSSD (g, h) in
swimmers across the training period (average ± SD). Note: # p < 0.05 vs. previous value.
3.2. Sleep
Average duration of sleep ranged from 7.32 ± 1.04 to 8.73 ± 0.69 h per day between subjects,
with no change in weekly sleep duration over the training period (Figure 1). Within a week,
swimmers were getting less sleep on Mondays compared with any other day (p < 0.05 in all cases, OP
= 0.99) and particularly compared with Sundays (>1 h, p < 0.05).
3.3. Resting HRV (lnRMSSD)
During the training period, the group average values of HR, RMSSD, and lnRMSSD were 68.6 ±
6.9 bpm, 73.0 ± 24.7 ms, and 4.23 ± 0.35 ms, respectively. Weekly variation in resting lnRMSSD
reached significance in weeks 5 and 6 (p < 0.05 compared with the previous week) (Figure 1) but was
generally minimal and usually did not coincide with training volume peaks. Interestingly, morning
lnRMSSD showed a progressive decrease within each week from a peak on Sundays and Mondays
to the lowest values on Fridays (p < 0.05, OP = 0.98). In addition, lnRMSSD decreased from 4.52 ± 1.91
to 4.32 ± 1.73 ms after 3–5 days of high total training volume (> 6 km/day), and increased from 4.09 ±
1.63 to 4.29 ± 1.54 ms after 3–5 days of rest (p < 0.05 in both cases).
Figure 1.
Total (
a
,
b
) and high-intensity (
c
,
d
) training volume, sleep (
e
,
f
) and lnRMSSD (
g
,
h
) in
swimmers across the training period (average ±SD). Note: # p<0.05 vs. previous value.
3.2. Sleep
Average duration of sleep ranged from 7.32
±
1.04 to 8.73
±
0.69 h per day between subjects, with
no change in weekly sleep duration over the training period (Figure 1). Within a week, swimmers
were getting less sleep on Mondays compared with any other day (p<0.05 in all cases, OP =0.99) and
particularly compared with Sundays (>1 h, p<0.05).
Int. J. Environ. Res. Public Health 2020,17, 2097 6 of 12
3.3. Resting HRV (lnRMSSD)
During the training period, the group average values of HR, RMSSD, and lnRMSSD were
68.6 ±6.9 bpm
, 73.0
±
24.7 ms, and 4.23
±
0.35 ms, respectively. Weekly variation in resting lnRMSSD
reached significance in weeks 5 and 6 (p<0.05 compared with the previous week) (Figure 1) but was
generally minimal and usually did not coincide with training volume peaks. Interestingly, morning
lnRMSSD showed a progressive decrease within each week from a peak on Sundays and Mondays to
the lowest values on Fridays (p<0.05, OP =0.98). In addition, lnRMSSD decreased from
4.52 ±1.91
to
4.32
±
1.73 ms after 3–5 days of high total training volume (>6 km/day), and increased from
4.09 ±1.63
to 4.29 ±1.54 ms after 3–5 days of rest (p<0.05 in both cases).
3.4. Correlations between Daily HRV, Training Volume, and Sleep Quantity
Individual day-to-day lnRMSSD values varied up to 50% across the training period (p<0.05)
(Table 2). There was a weak inverse correlation (r>
−
0.10) of lnRMSSD with total swimming volume
for 14 of the 22 subjects, which reached significance in only five swimmers (r>
−
0.27, p<0.05).
The correlations of lnRMSSD day-to-day variability with HI training volume or sleep volume were even
more trivial and unpredictably shifted from positive to inverse depending on the subject. A moderate
inverse relationship was detected between lnRMSSD and large shifts in total training volume (r=
−
0.35,
p<0.05 in cases of a >7.0 km/day swimming volume increase/decrease) (Figure 2). No significant
correlations were detected between lnRMSSD and small or moderate fluctuations (increase/decrease
by >3.0 or >5.0 km/day) in total volume or HI training volume.
Table 2.
Individual values of R–R intervals (RMSSD) converted by logarithmic transformation
(lnRMSSD) across the training period and correlations (Correl) with total and high-intensity (HI)
training and sleep duration.
LnRMSDD, ms Correl LnRMSDD
No Gender Average Max Min SD CV% Training Volume HI Volume Sleep
1 M 4.30 4.91 3.61 0.29 6.7 −0.05 −0.02 −0.01
2 M 4.25 4.88 2.20 0.36 8.5 −0.22 −0.24 −0.13
3 M 4.53 4.99 4.04 0.21 4.6 −0.07 −0.03 −0.13
4 M 3.90 5.19 3.18 0.44 11.3 −0.05 0.28 −0.03
5 M 4.61 5.08 4.13 0.20 4.3 −0.31 #0.11 −0.02
6 M 4.47 5.24 3.71 0.35 7.8 −0.18 0.05 −0.08
7 M 4.18 4.92 3.78 0.25 6.0 −0.09 0.11 −0.22
8 F 4.62 5.05 3.91 0.24 5.2 −0.08 0.30 −0.17
9 F 4.12 4.85 3.00 0.37 9.0 −0.28 #0.04 −0.06
10 F 3.60 4.43 2.30 0.44 12.2 −0.20 −0.01 0.00
11 F 3.38 4.29 2.40 0.41 12.1 −0.22 −0.12 0.06
12 F 3.65 3.99 3.22 0.18 4.9 −0.20 −0.06 −0.08
13 F 4.26 5.00 3.26 0.31 7.3 −0.05 0.25 −0.27
14 F 3.80 5.06 2.48 0.59 15.5 −0.17 0.23 0.41 #
15 F 4.84 5.32 4.20 0.23 4.8 −0.03 −0.21 −0.04
16 F 4.21 4.69 3.56 0.23 5.5 −0.06 −0.10 −0.16
17 F 4.59 5.13 3.71 0.36 7.8 −0.16 0.15 −0.05
18 F 4.03 5.00 3.26 0.38 9.4 −0.27 #0.02 −0.08
19 F 4.19 4.68 3.09 0.29 6.9 −0.29 #0.26 0.30 #
20 F 3.95 4.89 2.83 0.55 13.9 −0.45 #0.03 −0.26
21 F 4.23 4.90 3.4 0.35 8.3 −0.16 0.21 −0.04
22 F 4.01 5.32 3.18 0.37 9.2 −0.17 −0.03 0.21
Mean 4.17 4.90 3.29 0.34 8.1 −0.17 0.06 −0.04
SD 0.37 0.33 0.59 0.11 3.1
Note: M, male; F, female; SD, standard deviation; CV, coefficient of variation; HI, high-intensity training volume;
#p<0.05.
Int. J. Environ. Res. Public Health 2020,17, 2097 7 of 12
Int. J. Environ. Res. Public Health 2020, 17, x FOR PEER REVIEW 7 of 12
Figure 2. Correlations between individual values of RMSSD shifts and total (a, b, c) or high-intensity
(HI, d) training volume shifts. Note: * p < 0.05.
4. Discussion
The main finding of the study was a quite consistent reduction in HRV in response to markedly
increased training load such as a sharp increase in training volume or maintenance of high training
volume for 3–5 consecutive days. By contrast, day-to-day HRV in general reflected poorly
swimming training volume or sleep quantity, although this was also highly individual. These
findings suggest that measurement of morning HRV under home-based conditions could be
included as an indicator of the balance between the magnitude of the physical load and the young
athlete’s tolerance capacity within the intensified training periods.
The data obtained in the present study support the current understanding that HRV monitoring
does not allow the separation and classification of different subcategories of stress, but may be
useful in helping the practitioner to recognize the overall fatigue level [26,27]. It is quite well
established that one of the most popular HRV indexes, lnRMSSD, decreases considerably in
response to extreme loading, reflecting decreased vagal (parasympathetic) heart control, and this is
often associated with athlete fatigue and impaired performance [2,7,16,28–31]. Our study found that
during the days when training volume was high, lnRMSSD on the following morning was lower
than weekend values. Bearing in mind that our subjects were young but otherwise well-trained
swimmers who were expected to cope well with individual programs adapted to their age, gender,
training history, and ability level, the data suggest that observed fluctuations in HRV are of practical
value in sports training. Similar results have been observed in a number of studies that required
extended cardiac demands in response to endurance exercise training [16,29,32]. For instance,
alterations in resting autonomic function as reflected by changed HRV have been associated with
functional overreaching in triathletes [33] or injury incidence in swimmers [15].
In the setting of the current study, it was expected that day-to-day HRV monitoring would help
detect stress and recovery levels in young swimmers over the preparatory training period of 11
weeks. With this information in hand, coaches would be able to more precisely prescribe the training
loads for each workout according to the athlete’s condition in a given timeframe and hence better
prevent young athletes from excessive fatigue and insufficient recovery, leading to overloading,
overreaching, overtraining, and associated negative outcomes such as staleness, injuries, or lack of
progress. There was no significant instability of resting HRV in any of the subjects during the whole
Figure 2.
Correlations between individual values of RMSSD shifts and total (
a
,
b
,
c
) or high-intensity
(HI, d) training volume shifts. Note: * p<0.05.
4. Discussion
The main finding of the study was a quite consistent reduction in HRV in response to markedly
increased training load such as a sharp increase in training volume or maintenance of high training
volume for 3–5 consecutive days. By contrast, day-to-day HRV in general reflected poorly swimming
training volume or sleep quantity, although this was also highly individual. These findings suggest
that measurement of morning HRV under home-based conditions could be included as an indicator of
the balance between the magnitude of the physical load and the young athlete’s tolerance capacity
within the intensified training periods.
The data obtained in the present study support the current understanding that HRV monitoring
does not allow the separation and classification of different subcategories of stress, but may be useful in
helping the practitioner to recognize the overall fatigue level [
26
,
27
]. It is quite well established that one
of the most popular HRV indexes, lnRMSSD, decreases considerably in response to extreme loading,
reflecting decreased vagal (parasympathetic) heart control, and this is often associated with athlete
fatigue and impaired performance [
2
,
7
,
16
,
28
–
31
]. Our study found that during the days when training
volume was high, lnRMSSD on the following morning was lower than weekend values. Bearing
in mind that our subjects were young but otherwise well-trained swimmers who were expected to
cope well with individual programs adapted to their age, gender, training history, and ability level,
the data suggest that observed fluctuations in HRV are of practical value in sports training. Similar
results have been observed in a number of studies that required extended cardiac demands in response
to endurance exercise training [
16
,
29
,
32
]. For instance, alterations in resting autonomic function as
reflected by changed HRV have been associated with functional overreaching in triathletes [
33
] or
injury incidence in swimmers [15].
In the setting of the current study, it was expected that day-to-day HRV monitoring would help
detect stress and recovery levels in young swimmers over the preparatory training period of 11 weeks.
With this information in hand, coaches would be able to more precisely prescribe the training loads
for each workout according to the athlete’s condition in a given timeframe and hence better prevent
young athletes from excessive fatigue and insufficient recovery, leading to overloading, overreaching,
overtraining, and associated negative outcomes such as staleness, injuries, or lack of progress. There
was no significant instability of resting HRV in any of the subjects during the whole monitoring period,
Int. J. Environ. Res. Public Health 2020,17, 2097 8 of 12
indicating that excessive training loads had been avoided. However, for the optimization of progress
in performance, sufficient training loads are required during at least some of the weekly training
sessions (as after several consecutive days of intensified training, or HI training), and thus it could
be speculated that some degree of the change in resting HRV should be desirable as indicating the
triggering of beneficial adaptations. On a group level, daily lnRMSSD variations did not correlate
well with the previous day’s load and there was frequently inconsistent shifting of lnRMSSD in the
direction opposite to that expected. Individual changes were more predictable, but still the change
was significant in only five of the 22 subjects (<25%). Possible reasons for such discrepancies between
the individual and group level analyses have been described comprehensively elsewhere [
34
,
35
],
and include large interindividual differences between athletes in HRV parameters at baseline, HRV
changes during training, age, gender, perceived efforts, and anxiety. Of interest, we noted a tendency
of daily HRV variability to better reflect training load in the adolescents with low adherence to training
and low total swimming load in general; in addition, greater vagal activity was associated with smaller
fluctuations lnRMSSD across training days.
It was rather unexpected that values of day-to-day HRV (lnRMSSD) did not correlate with the
duration of night sleep. Sleep is indispensable for recovery and performance progress in athletes [
36
,
37
].
It is well established that the autonomic nervous system plays an important role in the modulation
of cardiovascular functions during the onset of sleep and in transition between sleep phases [
38
].
However, variation in the duration of sleep did not emerge as a significant influence on regulation
of the autonomic nervous system in the current study, which included no external manipulation of
sleeping patterns. However, it could hypothetically be that the association was masked because of the
timing of HRV measurement, which occurred not during the night sleep but only for 2 min after the
morning awakening. It is also possible that HRV is more sensitive to sleep quality and consistency
rather than the total duration of sleep [
6
], but analysis of this was outside the scope of the current study.
For the sake of simplicity, we used easily accessible devices and limited HRV analyses to the single
parameter of RMSSD, which was transformed to lnRMSSD. Measuring RMSSD alone might not give
a full picture of the mechanisms underlying changes in cardiac autonomic regulation [
8
,
27
,
39
]. However,
we consider that simplicity of monitoring and its interpretation are essential to encourage usage of
HRV measurement as a valid tool in sports practice. HRV recording is relatively straightforward
because numerous free applications have been developed for regular smartphones [
4
]. In addition,
although the recorded HRV data could be available almost instantaneously to the coach or other staff
of the sports team for inspection, analysis, and feedback, the interpretation of HRV and its changes is
not simple because response magnitude and timing are individually determined by multiple factors
including biological variation, emotions, and training context [2,27,40–42].
4.1. Limitations
Several limitations of the current study should be acknowledged. Although the subjects
participated in several sessions devoted to learning the HRV recording procedure and a one-week
familiarization period, the data from which were not included in the analysis, it was not possible
to monitor the HRV measurement procedure during the study to ensure that it had always been
conducted correctly. However, the familiar home environment and absence of the researchers allowed
the procedure to be at least well standardized and to obtain data not affected by additional stressors.
It could well be that timing of the HRV measurements did not allow estimation of the real impact
of the training loads on HRV, because the training sessions were typically half a day apart from the
HRV recordings; i.e., subjects might have either fully or partially recovered from the most recent
training session after the night’s rest (with additional recuperation until the next workout), or they had
accumulated additional stress during the day up to training. These aspects might have diminished the
reported associations between training loads and HRV.
Circadian rhythms have also been linked to HRV [
43
,
44
]. The subjects in the current study, all
schoolchildren, were waking up and measuring HRV in the morning at quite consistent times during
Int. J. Environ. Res. Public Health 2020,17, 2097 9 of 12
the week (except in some rare cases when they had training sessions early in the morning) but later
on weekends. Both of these factors possibly contributed to variability or bias of the recorded data,
with the longer sleep duration during weekends affecting HRV not only because of the longer rest, but
also because of the later time of the measurement, and the more relaxed approach when there were no
school activities or training sessions planned.
We neither controlled nor recorded the subjects’ diet, fluid, and food supplementation but the HRV
measurements were always conducted in the fasted state just after awakening, which mitigates the
possible effects of fluctuations in dietary intake during the previous day. Finally, biochemical measures
of stress such as cortisol to testosterone ratios would possibly have been useful in the interpretation of
the relationship of HRV with training loads and recovery [45].
4.2. Practical Application and Recommendations
Morning HRV could be consistently and reliably recorded on a daily basis by young (teenage
schoolchildren) competitive athletes in their home environment by means of commercially available
monitors and without supervision from parents, coaches or researchers. Morning HRV appears to be
a potential marker of the internal training load during the intensified training of young swimmers.
However, morning HRV weakly reflected the day-to-day fluctuations of training volume or intensity.
Therefore, simultaneous collection of additional subjective self-reported data such as perceived exertion
of each of the training sessions, as well as perceived sleep quality, amount of stress, muscle fatigue
and soreness by using customized questionnaires on a daily basis could be recommended for the
more thorough evaluation of the changes in athletes’ wellness [
46
] which could be of use in making
decisions for the adjustments in training loads. More demanding training load monitoring tools, such
as biochemical markers [47–49], could be considered to be included into the training monitoring.
5. Conclusions
This study showed a quite consistent reduction in HRV in response to markedly increased training
loads for several consecutive days. Although highly individual, day-to-day fluctuations in the morning
HRV was not consistently associated with swimming training volume or sleep quantity. Taken together,
these findings suggest that HRV fluctuations have limited value to quantify the balance between
the magnitude of the physical load and young athletes’ tolerance capacity, although under sharply
increased training load or extended periods of high volume training conditions, it may play a relatively
important role.
Author Contributions:
Conceptualization, S.K., T.V; methodology, A.S., M.M., N.E., J.S.; investigation, A.J., A.B.,
J.S., A.S., I.J.Z., M.M; formal analysis, A.J., M.M, A.B., N.E; writing—original draft preparation, S.K., B.H.O. and
T.V.; writing—review and editing, S.K., B.H.O. and TV.; All authors have read and agreed to the published version
of the manuscript.
Funding: This research received no external funding.
Acknowledgments:
Authors wish to thank Justas Achramaviˇcius, Žaneta Tautvyd
˙
e, Rasa Duškinien
˙
e, Aušra
Jureviˇcien
˙
e, Dita Kareckien
˙
e, Ram
¯
unas Leonas, Dainius Mažutaitis, J
¯
urat
˙
e Povilaitien
˙
e, Rimvydas Šalˇcius for their
assistance with data collection. We also are very thankful to the athletes for their active participation, and we also
would like to express our sincere thanks to the administrative staffof Kaunas Swimming School.
Conflicts of Interest: The authors declare no conflict of interest.
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