Influence of maternal physical exercise on fetal and maternal heart rate responses
This study aims to determine if regular maternal physical exercise leads to measurable adaptations of the fetal autonomic nervous system (fANS) tested by fetal heart rate recovery time. A randomized controlled trial enrolled 131 pregnant women into two study groups, Exercise Group (EG) and Control Group (CG). All participants signed an informed consent, study was approved by the local Clinical Research Ethics Committee. Data was analyzed on 81 participants.
EG participants (n = 43) received a supervised physical exercise program (PEP) three times a week from 10–12 to 36–40 weeks gestation. CG participants (n = 38) did not receive any supervised PEP. All women were tested between 34–36 weeks gestation using two walking tests of three minutes each at 40% and 60% maternal heart rate reserve. Resting fetal heart rate (FHR), FHR post-maternal exercise, and fetal recovery time (FRT) in minutes/seconds (m/s) were recorded. Resting FHR was similar between groups 140.88 ± 9 EG vs 141.95 ± 7.35 CG (p > .05). Difference in resting to post-maternal exercise FHR was statistically significant in fetuses from the CG (p < .05), however was not statistically significant in fetuses from the EG (p > .05). FRT was different between groups after both tests: 40% test: 2m15s ± 3m19s EG vs 7m6s ± 5m28s CG (p < .001); 60% test: 3m ± 4m3s EG vs 9m25s ± 7m33s CG (p < .001). There were no significant differences in maternal variables (p > .05), except for maternal recovery time after 40% test (p < .05). Influence of maternal exercise in FHR response still remains unclear. Further research is needed to elicit a former conclusion on the effects of maternal exercise on fANS. Overall, exercise during pregnancy is safe and not harmful for the cardiovascular system of the fetus.
KeywordsPhysical activity Pregnancy Cardiovascular health Autonomic nervous system Antenatal training
Einfluss der mütterlichen sportlichen Aktivitäten auf die Reaktion der fetalen und mütterlichen Herzfrequenz
Die vorliegende Studie hat das Ziel zu untersuchen, ob regelmäßige sportliche Aktivität von werdenden Müttern messbare Veränderungen im fetalen autonomen Nervensystems (fANS) hervorruft. Dies wurde anhand der fetalen Herzratenerholungszeit getestet. In einer randomisiert kontrollierten Studie wurden 131 schwangere Frauen entweder einer Sportgruppe (SG) oder einer Kontrollgruppe (KG) zugeteilt. Alle Versuchspersonen unterschrieben eine Einverständniserklärung und die Studie wurde durch das lokale Ethikkommission für klinische Forschung genehmigt. Es wurden Daten von 81 Teilnehmerinnen analysiert. Die Teilnehmerinnen der SG (n = 43) erhielten jeweils in der 10.–12. und 36.–40. Schwangerschaftswoche drei betreute Sporteinheiten. Die Teilnehmerinnen der Kontrollgruppe (n = 38) blieben ohne betreutes Sportprogramm. Alle Frauen wurden während der 34. und 36. Schwangerschaftswoche getestet. Dazu wurden zwei Geh-Tests à 3 Minuten bei 40 % und 60 % Herzfrequenzreserve durchgeführt. Es wurde die fetale Ruhe-Herzfrequenz (FHF), die FHF nach sportlicher Aktivität der Mutter und die fetale Erholungszeit (FEZ) in Minuten/Sekunden (min/sek) gemessen. Die Gruppen zeigten eine ähnliche Ruhe-FHF: 140,88 ± 9 (SG) vs 141,95 ± 7,35 (KG) (p > .05). Föten in der KG, nicht aber in der SG, zeigten einen signifikanten Unterschied in ihrer Herzfrequenz nach sportlicher Aktivität der Mutter, verglichen mit der Ruhe-Herzfrequenz. Die FEZ der Gruppen unterschied sich in beiden Geh-Tests: 40 %-Test: 2 min 15 sek ± 3 min 19 sek (SG) vs. 7 min 6 sek ± 5 min 28 sek (KG) (p > .001); 60 %-Test: 3 min ± 4 min 3 sek (SG) vs. 9 min 25 sek ± 7 min 33 sek (KG) (p < .001). Für die Mütter ergaben sich außer in der Erholungszeit nach dem 40 %-Test (p < .05) in keiner der erhobenen Variablen signifikante Unterschiede (p > .05). Der Einfluss der sportlichen Aktivität von werdenden Müttern auf die fetale Herzrate bleibt unklar. Weitere Forschung ist erforderlich, um Schlussfolgerungen zu den Auswirkungen der sportlichen Aktivität von werdenden Müttern auf das fANS zu ziehen. Insgesamt betrachtet, ist sportliche Aktivität während der Schwangerschaft als sicher und nicht schädlich für das kardiovaskuläre System des Fötus einzustufen.
SchlüsselwörterKörperliche Aktivität Schwangerschaft Kardiovaskuläre Gesundheit Autonomes Nervensystem Pränatales Training
Though exercise during pregnancy is becoming an increasingly common activity, many pregnant women are not aware of the benefits for themselves and their fetus. There is growing evidence to support the safety of exercise during pregnancy, yet universal guidelines and recommendations from healthcare professionals lag behind the research (ACOG, 2015; Evenson, Barakat, & Brown, 2014; Mottola et al., 2018; Zavorsky & Longo, 2011). For example, between 2002 and 2015 there were no updates to the American College of Obstetricians and Gynecologists (ACOG) guidelines (ACOG, 2002, 2015). Although research supports the efficacy and safety of exercise during pregnancy (ACOG, 2015; Bø et al., 2016; Evenson et al., 2014; Mottola et al., 2018), there are few randomized controlled trials during gestation to evaluate fetal and maternal heart rate response during and following exercise. By monitoring fetal heart rate (FHR) during and after exercise, it is possible to determine the influence of maternal physical activity on key markers of fetal health, such as autonomic nervous system (ANS) functioning (May, Glaros, Yeh, Clapp, & Gustafson, 2010).
Based on the Barker theory, maternal behaviors influence intrauterine environment which thus influence the fetus after birth and into adulthood. Therefore, if maternal harmful habits during pregnancy influence fetal development to lead to disease in adult life (Barker, 2007), then healthy maternal habits may promote health of the fetus into adulthood as well (Bahls et al., 2014).
Chronic cardiovascular exercise in adults leads to adaptations of the ANS evidenced by lower heart rate (HR) at rest, exercise and recovery (Barbosa, Valente, Sobral, & Barbosa, 2015; Ostojic et al., 2010). Based on Barker’s theory, similar adaptations should occur to the fetus in utero in response to chronic maternal exercise. Research performed in 2010 showed lower HR and increased HR variability at rest, an indicator of improved ANS control, in fetuses from pregnant exercisers compared to fetuses of non-exercisers (May et al., 2010). These findings are similar to the adaptations of an exercise-trained adult (Roldan, Perales, Mateos, & Barakat, 2015) and suggest an improved functioning of fetal ANS (May, Allen, & Gustafson, 2016; May et al., 2010).
Other indicators of this beneficial adaptations of the fetal ANS as a consequence of maternal physical activity would further support the Barker theory and the possibility of a fetal training effect from chronic maternal exercise exposure (Roldan et al., 2015). Recovery time after maternal exercise is a feasible variable to measure in the fetus and is known to improve in adults in response to exercise training (Barbosa et al., 2015; Heffernan, Fahs, Shinsako, Jae, & Fernhall, 2007; Ostojic et al., 2010; Ostojic, Stojanovic, & Calleja-Gonzalez, 2011). Although fetal heart rate (FHR) recovery time will offer novel insights to adaptations of fetal ANS as a consequence of maternal exercise, this variable has not been evaluated in fetuses as a primary aim.
Thus, the objective of this study is to determine if regular maternal physical activity leads to measurable adaptations of the fetal ANS measured by FHR response recovery time. We hypothesized the FHR recovery would be shorter (quicker) in those exposed to maternal exercise relative to those not exposed to maternal exercise.
The present study is part of a randomized controlled trial (ID: RCT, NCT01723293) that was conducted between 2010 and 2015. It was a collaborative effort between the Faculty of Sport Science and Physical Activity of the Technical University of Madrid (Spain) and three local hospitals in Madrid. The study was conducted following the principles of the Declaration of Helsinki.
We recruited pregnant women for this study between September 2011 and January 2015. The study was approved by the Clinical Research Ethics Committee of the University Hospital of Fuenlabrada, Severo Ochoa University Hospital and the University Hospital of Puerta del Hierro. All participants were recruited from obstetrical consulting at these three local hospitals. All women signed written informed consent for inclusion in the study; they also completed the participant’s information sheet with the study characteristics.
All participants had no absolute obstetric contraindications to exercise (ACOG, 2015). Women were 25–40 years old and all were living within the community of Madrid. All participants were carrying a single fetus and had no history of alcohol or drug use. Participants were instructed not to participate in other physical activity programs. They were required to give birth at one of the three participating hospitals and were required to understand and speak Spanish fluently. Participants in the exercise group needed to maintain an 75% adherence to the exercise protocol.
Participants were randomized into two groups: an exercise group (EG) and a control group (CG). EG participants received an intervention based on a physical activity program. CG participants did not receive the intervention and were not encouraged to exercise. All participants had normal obstetric appointments and received the same standard health care.
Physical activity program
A physical activity program was designed following ACOG guidelines (ACOG, 2002) and the Blooming Exercise Program (Pelaez, 2011), an exercise program developed in Spain specifically for pregnant women. The EG began the program at 10–12 weeks gestation until 36–40 weeks gestation, three days per week. Each session lasted 60 min and included the following: warm up for 5–7 min, aerobic dance for 25–30 min, strength training for 8–10 min, pelvic floor muscle training for 8–10 min, stretching for 3–5 min.
The intensity was measured using heart rate (HR) target zones from 40 to 60% reserve heart rate (Zavorsky & Longo, 2011) for moderate intensity. Participants in EG wore a HR monitor (FT7 Polar Electro Oy, Finland) to ensure training within their target HR zone.
Fetal heart rate assessment protocol
All participants performed two walking tests, the first one at 40% maternal heart rate reserve (HRR), and the second one at 60% maternal HRR, between 34 and 36 weeks in one of three participating hospitals. These intensity targets were selected because they are the recommended intensity for exercise during pregnancy (Barakat, Ruiz, Rodríguez-Romo, Montejo-Rodríguez, & Lucia, 2010; Barakat, Stirling, Zakynthinaki, & Lucía, 2008; Szymanski & Satin, 2012; Zavorsky & Longo, 2011). This target HR zone is safe and is not associated with harmful effects for mother and fetus. Each walking test began with a three minute warm up for safety and to ensure target HR, immediately afterwards the walking test was performed and lasted three minutes. Test length is short enough for all participants to complete, but long enough to produce maternal and fetal physiological responses (Brenner, Wolfe, Monga, & McGrath, 1999; Rafla & Cook, 1999). At 34–36 weeks of gestation, the fetal heart and circulatory system have completed structural changes making heartbeat recordings easier (Sadler, 2010). This period also provides 20 weeks of exercise exposure for the fetus in the exercise group and thus long enough to elicit fetal adaptations (May et al., 2010).
The day of the test women were instructed to eat a snack 90 min before the test. During the first 20 min, resting maternal and FHR were recorded using a HR monitor (FT7 Polar Electro Oy, Finland) and a wireless FHR monitor (Wireless Telemetry T800 Hispania Hospital S.L Spain) respectively (Roldan et al., 2015). Maternal HR at rest was established as the lowest value recorded on the HR monitor during the 20 min resting period. Target HR for each test was obtained using the Karvonen Formula (target heart rate = (HRR × intensity of the exercise) + RHR). Where HRR is heart rate reserve and RHR is resting heart rate. HRR was obtained using the following formula (maximal HR − resting HR). Maximal HR was calculated with the equation 220 − age; and resting HR was obtained from the resting period at the beginning of the testing protocol. Intensity of the exercise was 40 or 60% of the HRR; the fraction of the intensity, 0.4 and 0.6 respectively, were included in the equation for each walking test.
Resting FHR or baseline FHR was estimated following Royal College of Obstetricians and Gynaecologists and the National Institute for Clinical Excellence (RCOG/NICE) guidelines for cardiotocography (CTG) interpretation (Ayres-de-Campos & Bernardes, 2010; RCOG, 2001).
Once resting maternal HR and baseline FHR were recorded, each participant performed a three-minute warm-up followed immediately by the three-minute walking test at 40% HRR intensity. During the three minutes walking test, maternal HR was continuously recorded and checked to validate the participant was within the target HR for the given intensity. A range of ±2 bpm was allowed. With the use of wireless sensors, FHR was continuously monitored during this time.
Once the first walking test was finished, FHR was labelled as FHR after maternal exercise. Maternal and fetal HR recovery time were recorded as well. Since it is not recommended to sit immediately after exercise, participants remained standing during the first 5 min of recovery (ACSM, 2014). After 5 min, participants were able to sit in a comfortable chair. The maximum time for recovery was set at 20 min.
Recovery was defined as the return to resting (baseline) maternal and fetal HR. Maternal HR recovery time was defined as the time required to return to the resting (baseline) HR measured during the initial 20-minute resting period. FHR recovery time was defined as the time elapsed from the end of the walking test to the time that FHR returned to the baseline value. Maternal and fetal recovery time were recorded for 20 min. If FHR did not return to baseline within 20 min after the 40% test, then we waited until FHR was at baseline levels or ±5 bpm of baseline before proceeding to the 60% test. Once this recovery period was completed, the second test at 60% HRR intensity was performed. The three-minute walking test at 60% HRR intensity was performed following the same procedure as the first walking test.
Our primary outcome variable was FHR recovery time. The secondary outcome variables were FHR at rest, FHR after exercise, and difference between these timepoints; as well as, percentage of fetuses recovered by 20 min, maternal HR at rest, maternal HR at after exercise, and maternal HR recovery time.
All statistical analyses were performed using the Statistical program SPSS 20.0 version for PC with α level <0.05 a priori. Shapiro–Wilk test was performed in all variables to test normality of the data. Results from this test showed a non-normal distribution of the data in the following variables: baseline FHR at rest, FHR recovery time in both tests, maternal HR at rest, maternal HR at the end of both tests and maternal HR recovery time. Therefore, non-parametric Mann–Whitney U test was performed to analyze differences in variables with non-normal distributions. Spearman correlations were used to evaluate correlations in maternal and fetal recovery time. T‑tests for unpaired samples were performed to analyze mean differences in FHR after exercise between groups. All data are presented as mean ± standard deviation (SD). Due to signal loos of the FHR during maternal exercise, we were aunable to analyze this variable.
In all, 199 pregnant women were recruited for the study. All women met inclusion criteria to participate in the study. From the 199 assessed for eligibility, 68 were excluded (Fig. 1). Of those remaining, 131 were randomized into EG, n = 64, and CG, n = 67, (Fig. 1) following a Simple Random Sampling protocol (Armitage & Berry, 2002).
From the 131 pregnant women randomized, only 81 were included in data analysis (Fig. 1). All 81 women had healthy, uncomplicated pregnancies (43 EG, 38 CG). Baseline characteristics (mean ± SD) were similar between groups: age (32.6 ± 4 years in EG; 32.6 ± 3.5 years in CG), prepregnancy weight (60.9 ± 9.1 kg in the EG; 62.9 ± 10 kg in the CG), and prepregnancy BMI (22.3 ± 3.2 in the EG; 23.4 ± 3.4 in CG). All participants delivered healthy babies (41 male vs 40 female): birth weight (g) (3139.00 ± 476.86 EG vs 3222.41 ± 416.62 CG; p > 0.05); height (cm) (49.62 ± 2.61 EG vs 49.51 ± 2.41 CG; p > 0.05); head circumference (cm) (34.34 ± 1.29 EG vs 34.60 ± 1.46 CG; p > 0.05); Apgar score 1 min (8.93 ± 1.18 EG vs 9.09 ± 0.77 CG; p > 0.05); Apgar score 5 min (9.67 ± 1.21 EG vs 9.88 ± 0.42 CG; p > 0.05). Two offspring from EG and one from CG had low birth weight (<2.5 kg); two offspring from EG were macrosomic (>4 kg), none from the CG.
Fetal heart rate (FHR) responses
CG (n = 38)
EG (n = 43)
Resting FHR (beats/min)
141.9 ± 7.3
140.8 ± 9.4
FHR after maternal exercise 40% (beats/min)
147.8 ± 12.5
139.9 ± 13.4
FHR recovery time 40% (min/s)
7 min 6 s ± 5 min 28 s
2 min 15 s ± 3 min 19 s
FHR after maternal exercise 60% (beats/min)
148.0 ± 15
143.7 ± 10.4
FHR recovery time 60% (min/s)
9 min 25s ± 7 min 33 s
3 min 0 s ± 4 min 3 s
Comparison of fetal heart rate (FHR) at rest and FHR post-exercise within groups
CG (n = 38)
FHR at rest (beats/min)
FHR post-exercise (beats/min)
Walking test at 40%
141.9 ± 7.3
147.8 ± 12.5
Walking test at 60%
141.9 ± 7.3
148.0 ± 15
EG (n = 41)
FHR at rest (beats/min)
FHR post-exercise (beats/min)
Walking test at 40%
140.8 ± 9.4
139.93 ± 13.48
Walking test at 60%
140.8 ± 9.4
143.7 ± 10.4
The percentage of fetuses that recovered within 20 min after maternal exercise was analyzed for both three-minute walking tests between groups. Of the fetuses in EG, 100% (43/43) recovered within 20 min after both walking test. Of the fetuses in CG, 94.7% (36/38) and 81.6% (31/38) recovered within 20 min after the 40% intensity and 60% walking test, respectively. We did not observe any episodes of bradycardia or tachycardia within CTG recordings from those fetuses. However, significantly fewer fetuses from the CG achieved recovery to resting FHR within 20 min following the 60% intensity test (p <0.05).
Maternal HR during FHR assessment protocol
Maternal heart rate (HR) during fetal HR assessment protocol
CG (n = 38)
EG (n = 43)
Maternal HR at rest (beats/min)
88.2 ± 12.2
87.4 ± 11.3
Maternal HR at 40% (beats/min)
127.9 ± 7.6
127.2 ± 7.3
Maternal HR recovery at 40% (min/s)
8 min 31 s ± 4 min 37 s
6 min 49s ± 4 min 14 s
Maternal HR at 60% (beats/min)
147.8 ± 5.5
147.1 ± 5.5
Maternal HR recovery at 60% (min/s)
14 min 3s ± 5 min 32 s
11 min 49s ± 5 min 16 s
Correlation between maternal heart rate (MHR) recovery time and fetal heart rate (FHR) recovery time for both tests
CG (n = 38)
EG (n = 43)
MHR recovery time at 40%
FHR recovery time at 40%
FHR recovery time at 40%
MHR recovery time at 60%
FHR recovery time at 60%
FHR recovery time at 60%
We hypothesized that FHR recovery would be shorter (quicker) in fetuses exposed to maternal exercise relative to those not exposed to maternal exercise. We found significantly quicker FHR recovery times in the exercise group relative to the control group at both intensities. Similarly, we found significantly more exercise exposed fetuses recovered by 20 min compared to fetuses of controls. Interestingly, control fetuses had significant increases in FHR response to exercise, whereas fetuses of exercisers did not. Participants in the EG had significantly quicker maternal HR recovery time after the three-minute walking test at 40% intensity. Furthermore, there are trends towards significant differences in the maternal HR recovery time after the walking test at 60% intensity.
These findings are the first to demonstrate 100% of fetuses exposed to exercise at recommended levels have a quicker recovery to baseline after maternal exercise compared to fetuses not exposed to exercise in utero. The significant difference in fetal recovery time of approximately 5–6 min between groups is similar to previous study findings (Roldan et al., 2015), which shows reproducibility of this result.
Post-exercise recovery time between 5 to 7 min in CG foetuses is similar to previous research (Barakat et al., 2008). Similar to our EG, Rafla and Cook (1999) reported lower FHR immediately after maternal exercise in fetuses from active women relative to fetuses of sedentary women. However, Rafla and Cook did not measure recovery time of FHR.
A decreased HR recovery time after exercise is an indicator of ANS adaptation in adults exposed to chronic aerobic exercise training (Barak et al., 2011; Barbosa et al., 2015; Carter, Banister, & Blaber, 2003; Danieli et al., 2014; Wilmore & Costill, 2007). Therefore, a faster recovery time in fetuses from EG supports the idea of fetal ANS adaptation to chronic maternal exercise exposure. This finding is aligned with previous findings from May et al. (2010) which also found measures indicative of a more mature ANS function in fetuses from women who exercised during pregnancy. The finding that all EG fetuses recovered more quickly than CG fetuses after maternal exercise supports the positive influence of maternal exercise on fetal cardiac ANS development and thus the Barker hypothesis related to health outcomes and not just disease outcomes of offspring (Barker, 2007). This faster recovery could have occurred in EG fetuses due to a significantly lower FHR after maternal exercise in comparison with CG fetuses, as it can be seen after the 40% walking test. Although, after 60% walking test the between group difference in FHR after maternal effort is not statistically significant, showing a similar fetal cardiovascular response to the 60% walking test. Moreover, as it has been discussed above, FHR recovery after this test was significantly faster in fetuses exposed to chronic exercise. This fact also supports the positive influence of maternal exercise on fetal cardiac response.
Resting baseline FHR was lower in the EG compared to CG group, although this was not significant, most likely due to not controlling for fetal activity state (May et al., 2010; Schneider et al., 2009). Fetal state can influence baseline FHR, either increasing baseline FHR in active states or decreasing baseline FHR in the quiet states (Schneider et al., 2009). Therefore, analysing baseline FHR without controlling fetal state could have confounded this result.
There were significant differences between resting to post-maternal exercise FHR in fetuses of controls and not in fetuses of exercisers (Table 2). Lower HR after submaximal exercise is one of the main cardiovascular adaptations to aerobic exercise in young adults (Calderón, 2001; Carter et al., 2003; Cornelissen, Verheyden, Aubert, & Fagard, 2010; Wilmore & Costill, 2007). Although it is not completely understood, this adaptation is generally attributed to a reduction in the sympathetic activation during submaximal exercise (Carter et al., 2003). Therefore, a potential explanation for our finding is that it may demonstrate a fetal heart adaptation to chronic maternal exercise exposure similar to the one occurring in young adults. The fact that FHR in EG fetuses did not increase significantly from resting to post-exercise period could be due to the FHR responding closely to baseline levels and not being affected by a maternal effort as a consequence of the chronic exposure to exercise. Nevertheless, this FHR response could be also due to a flat or reduce response to the FHR. One research has been found with a similar exercise intervention to the one presented in our study (Brenner et al., 1999), which ease results comparison. Authors in this research found that FHR at rest and post maternal effort was not different in fetuses of women who exercise. Furthermore, this research shows an increase in FHR during maternal exercise, voiding the possibility of a flat response of FHR in these fetuses. To confirm an approximate response of FHR in our study to the FHR response found by Brenner et al. (1999) FHR during maternal exercise should have been evaluated. Nevertheless, we have been unable to provide that analysis due to recurrent signal loss in FHR recordings during both walking tests. Hence, the mechanisms through which fetuses in the EG had a lower FHR after maternal exercise still remains unclear.
A recent meta-analysis (Skow et al., 2018) studying FHR responses to maternal exercise concludes there is insufficient research to support a relevant response of FHR associated with chronic exercise. However, the studies included in the meta-analysis have different methods of exercise training (i. e. frequency, intensity, duration, type of exercise), which make a strong conclusion regarding FHR response to chronic maternal exercise difficult.
The maternal HR changes in the current study are similar to the results reported by others, showing a slightly lower, but not significant, resting HR in the EG (Perales et al., 2016; May et al., 2016) with improved HR variability (May et al., 2016). However, it seems that HR adaptations due to aerobic exercise are more difficult to detect during pregnancy most likely due to the naturally increasing resting HR, a sign of altered maternal ANS, as gestation progresses.
In relation to maternal HR recovery time, this result reached significance in the walking test at 40% showing a faster recovery in participants in the EG and, hence, an adaptation to aerobic exercise. This is the first study to demonstrate maternal HR recovery time in women who participated in an exercise program throughout gestation. However, studies evaluating cardiorespiratory physical fitness (CRF) reported higher CRF values in active pregnant women compared controls (Halse, Wallman, Dimmock, Newnham, & Guelfi, 2015; Ramírez-Vélez et al., 2011). The current study also a found similar trend towards improved HR recovery in the EG compared to the CG. These findings also serve to confirm an exercise adaptation on maternal physiology.
One study limitation was the recurrent FHR signal loss during maternal exercise, which made the FHR response during maternal exercise data unusable. Another limitation of the CTG is the difficulty evaluating FHR variability through the paper traces obtained from the recordings.
Despite of the limitations, novelty of this equipment comes from the possibility of testing FHR in a wireless environment. Using a wireless CTG equipment allows testing FHR responses in a realistic situation, as walking is, vs a laboratory situation. Hence, results obtained from this test could have been easily transferred to a situation more approximate to a daily activity. Although as it has been already mentioned, recurrent signal loss occurred during the walking section of the protocol.
Although we did not control for physical activities outside of the study protocol, the positive exercise response of women in the intervention group support their compliance with the study protocol. Though our study had positive findings, all participants were in the healthy range for body mass index (BMI); this makes the results difficult to generalize to the average pregnant population. Further research is needed to determine if similar results are seen in overweight and obese pregnant women.
These results support that supervised moderate intensity exercise during pregnancy at levels recommended by ACOG are associated with quicker FHR recovery time, which can be related to an improved fetal ANS function. Further research needs to be done to determine if these findings are also observed after birth.
The authors acknowledge to committee of the three local hospitals for their help and support during the study.
Compliance with ethical guidelines
Conflict of interest
O. Roldan-Reoyo, M. Pelaez, L. May and R. Barakat declare that they have no conflict of interests.
All procedures performed in studies involving human participants or on human tissue were in accordance with the ethical standards of the institutional and/or national research committee and with the 2013 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.
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