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Journal of Clinical Medicine logoLink to Journal of Clinical Medicine
. 2023 Jul 26;12(15):4915. doi: 10.3390/jcm12154915

Is Exercise during Pregnancy a Risk for Gestational Age and Preterm Delivery? Systematic Review and Meta-Analysis

Rubén Barakat 1, Dingfeng Zhang 1, Miguel Sánchez-Polán 1, Cristina Silva-José 1, Javier Gil-Ares 1,*, Evelia Franco 2
Editor: Eyal Sheiner
PMCID: PMC10419377  PMID: 37568315

Abstract

Traditionally, one of the primary concerns regarding exercise during pregnancy has been the potential of reducing gestational age and increasing the likelihood of preterm delivery. The aim of this study was to perform a systematic review about the effects of physical activity (PA) during pregnancy on gestational age and preterm delivery. A systematic review and two meta-analyses were performed (Registration No. CRD42022370770). Data sources from online databases were searched up to November 2022. The review exclusively included studies involving pregnant populations and interventions consisting of PA implemented during pregnancy. The primary outcomes analysed were gestational age, measured in weeks, and the occurrence of preterm deliveries. A total of 57 studies were analysed through two independent meta-analyses for the first one, no association was found between moderate exercise during pregnancy and gestational age (Z = 0.45, p = 0.65, ES = 0.08, 95% CI = −0.06−0.04, I2 = 42%, P heterogeneity = 0.001), showing the exercise group had a higher gestational age. In addition, no differences were found between groups in terms of number of preterm deliveries (RR = 0.96, (95% CI = 0.77–1.21, Z = 0.33, p = 0.74; ES = 0.07; I2 = 31%, P heterogeneity = 0.05)). The findings of this study indicate that there is no association between exercise during pregnancy and reduced gestational age or increased risk of preterm delivery in healthy pregnancies.

Keywords: pregnancy, exercise, gestational age, preterm delivery

1. Introduction

The intricate process of pregnancy and childbirth plays a crucial role in shaping the long-term health outcomes for both the mother and the child. Spanning over several months, it involves substantial modifications in nearly all of a woman’s bodily systems to support the growth and development of the foetus. Therefore, it is imperative to ensure the optimal functioning of all maternal physiological, mental, and emotional mechanisms that facilitate foetal growth and development. Any complications arising within these domains of health may contribute to pathologies and complications that adversely affect the well-being of both the mother and the newborn [1,2].

The numerous demands imposed by pregnancy transform the process of gestation and childbirth into a formidable challenge that women must navigate throughout the forty weeks of gestational age. Their goal is to avert pathologies and adverse outcomes, such as preterm delivery, which can give rise to significant associated complications [3,4].

Premature birth refers to the condition where a baby is born before the completion of a full-term pregnancy, which lasts approximately 40 weeks. Preterm birth, on the other hand, occurs when delivery takes place prior to the 37th week of pregnancy. Premature babies often encounter significant health challenges, particularly when born at earlier stages of gestation. The nature and severity of these problems can vary, with a higher risk of associated health complications observed as the gestational age decreases [5]. In this intricate scenario, it is crucial for pregnant women to prioritize the well-being of all aspects of their body, encompassing not only physiological factors but also mental and emotional aspects [6].

In light of scientific evidence, it is well-established that unhealthy lifestyles have negative implications for pregnancy outcomes. Engaging in an unhealthy lifestyle during pregnancy heightens the risk of chronic diseases [7]. Moreover, the escalating epidemic of obesity and sedentary habits significantly impacts pregnancy and childbirth, with enduring adverse consequences [8]. The scientific literature highlights the substantial benefits derived from various forms of physical activity (PA) in terms of pregnancy outcomes and overall health and well-being [9,10]. Nevertheless, the impact of PA during pregnancy on gestational age and preterm delivery has not been extensively investigated, leaving significant scientific gaps [11].

Achieving an optimal gestational age and preventing a preterm delivery are two crucial factors that significantly impact the well-being of both the mother and child during the pre-, peri-, and postnatal periods. Traditionally and historically, physical exercise during pregnancy has been inaccurately perceived as a challenging factor for both gestational age and preterm birth.

PA has become an integral component for diverse populations, including pregnant women. Many studies have confirmed the benefits of PA on different maternal, foetal, and newborn outcomes. Nevertheless, the impact of various types of PA on gestational age and preterm delivery has been inadequately examined through systematic reviews, resulting in a significant knowledge gap in this scientific domain. Through a rigorous analysis of the recent literature, it is evident that only a few studies with high reliability, such as systematic reviews with meta-analyses, have been conducted. Thus, studies with a rigorous scientific methodology and guaranteed reliability are essential to generate new evidence on this issue.

In this sense, in the recent scientific literature, only one systematic review study [12] has specifically investigated the effects of gestational PA on preterm delivery. The objective of this systematic review and meta-analysis is to examine the current scientific evidence concerning the effects of PA during pregnancy on gestational age and the occurrence of preterm delivery.

2. Materials and Methods

This study was developed following the Preferred Reporting Items for Systematic reviews (PRISMA) guidelines [13] and registered with the International Prospective Register of Systematics reviews (PROSPERO, registration No. CRD42022370770). Population, Intervention, Comparison, Outcomes and Study design framework (PICOS) was used to analyse the searching sources included in this research [14].

2.1. Population

Pregnant women without any obstetrical relative (e.g., gestational hypertension, malnutrition, or moderate cardiovascular disease) or absolute (e.g., premature labour, preeclampsia, or incompetent cervix) contraindications, participating in a PA programme during pregnancy were chosen.

2.2. Intervention

The intervention characteristics analysed were: (a) weekly frequency of PA sessions; (b) intensity: all studies included had a moderate intensity of load, using 55–65% of the maximum maternal heart rate or the perception of effort (range 12–14 of the Borg Scale); (c) duration of the PA program; (d) type of PA (e.g., yoga, Pilates, aerobic, strength, or pelvic floor training); (e) supervision or not of the PA program; (f) time duration of the sessions, as shown in Table 1.

2.3. Comparison

Women who engaged in an exercise or PA program during pregnancy were compared with those who did not participate in such a program. Intervention characteristics were retrieved and compared as shown in Table 1.

2.4. Outcomes

The gestational age (measured in weeks) and the preterm deliveries were the target outcome.

2.5. Study Design and Selection Process

The search for this study was done between September and November 2022, at Universidad Politécnica de Madrid (INEF). EBSCO (including Academic Search Premier, Education Resources Information Center, MEDLINE, SPORTDiscus, and OpenDissertations databases), Clinicaltrials.gov, Web of Science, Scopus, Cochrane Database of Systematic Reviews, and Physiotherapy Evidence Database (PEDro) were searched. More precisely, articles written in English or Spanish and published between 2010 and 2022 were searched.

The search terms were:

  • English: physical activity OR exercise OR physical exercise OR fitness OR strength training OR physical intervention OR cointervention AND pregnancy OR pregnant OR maternal OR antenatal AND randomized clinical trial OR RCT OR non-randomized clinical trial AND gestational age OR preterm birth OR preterm delivery.

  • Spanish: actividad física OR ejercicio OR ejercicio físico OR fitness OR entrenamiento de fuerza OR intervención física OR co-intervención AND embarazo OR embarazada OR maternal OR prenatal AND ensayo clínico aleatorizado OR ensayo clínico no aleatorizado AND edad gestacional OR nacimiento a pretérmino OR parto pretérmino.

Eligible articles for our review included studies that had a quantifiable PA or exercise intervention (excluding the articles with only advice to have an active pregnancy or those having a measurable PA questionnaire but without an exercise intervention), with gestational age or preterm delivery as outcomes, and with the characteristics of the PA or exercise program provided. This process is detailed in Figure 1.

Figure 1.

Figure 1

Flow diagram of the analysed articles.

The primary outcomes were gestational age and preterm birth. Studies reporting either of them were included in the review. Firstly, two reviewers (M.S.-P. and D.Z.) screened independently the studies retrieved in the search achieving a complete consensus in the decision about the eligible studies. In a second stage, two reviewers (M.S.-P. and C.S.) performed the data extraction from the included studies. In case of doubt at that stage, they consulted with the rest of the authors until an agreement on the appropriate manner to report the information from the study was reached. In cases where both gestational age and preterm delivery were reported in the same study, both measures were separately included in the meta-analysis. Additionally, to check the effects of each intervention on maternal health, other outcomes were examined (but not included in the meta-analyses) as secondary outcomes, such as physiologic, sociodemographic, and delivery outcomes. From each chosen study, we extracted the author(s), publication year, country in which the study was developed, type of study design, number of participants, characteristics of the intervention program, and variables analysed (primary and secondary) (Table 1).

2.6. Statistical Analysis, Quality of Evidence Assessment, and Risk of Bias

As mentioned earlier, two separate meta-analyses were performed. For the first meta-analysis including the studies reporting gestational age as a continuous variable, the overall confidence interval (CI) was calculated using the standardized mean difference [15]. For the second meta-analysis, the dependent variable was the ratio of preterm deliveries in each study, and it was expressed as a categorical variable (yes/no). In that case, the number of events present in each study group and its relative risk (RR) were recorded, and the total sum of the RR was calculated using a random-effects model [16]. In both analyses, each study had a relative weight assignment corresponding to its sample size number, which contributed to the entire analysis, establishing the compensated average. The I2 statistic was used to quantify the heterogeneity present in the results due to the different interventions and designs of each article, indicating the variability of the effect of each intervention, and whether it was random or not. The following considerations were used: low heterogeneity = 25%; moderate heterogeneity = 50%; and high heterogeneity = 75% [17]. Ferreira-González et al. [18] demonstrated that in the case of a high heterogeneity, one solution could be to divide the studies into subgroups performed with different characteristics explaining that variability. However, for our article with limited results, we understood that presenting all articles in each analysis would provide a better approach for the study.

For the assessment of the quality of evidence for the main outcome and each study, the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework was used, including studies rated as having a moderate or high quality [19]. To determine the potential risk of bias (with these sources: selection, performance, attrition, detection, and reporting bias), the Cochrane Handbook was followed [20]. Randomised clinical trials’ evidence initially started with a “low” risk of bias (due to the theoretical study design and intervention), compared to nonrandomised interventions, and both increased or decreased its risk of bias in function of having any “high” or “low” score across bias sources. Both the quality of the study and the risk of bias analyses were performed by three of the reviewers (M.S.-P., C.S., and E.F.).

Table 1.

Characteristics of the studies included in the review.

Author Year Country N EG CG Intervention Features Main Variables Analysed Secondary Variables Analysed
Freq Intensity PT Type Superv. Class Duration Adh.
Babbar [21] 2016 US 46 23 23 3 Mod 8 w Yoga Yes 60 min - Gestational age, type of delivery, birth weight Gestational weight gain
Bacchi [22] 2018 Argentina 111 49 62 3 Low–mod 26 w Aquatic activities Yes 55–60 min 80% Gestational weight gain, gestational age Birth weight
Backhausen [23] 2017 Denmark 516 258 258 2 Low 12 w Aerobic No 70 min - Low back pain, birth weight Gestational age, type of delivery
Barakat [24] 2011 Spain 80 40 40 3 Low–mod 28 w Aerobic and light strength training Yes 35–45 min Maternal health status Gestational age, type of delivery
Barakat [25] 2012 a Spain 290 138 152 3 Mod 28 w Aerobic exercise Yes 40–45 min - Type of delivery Gestational age and birth weight
Barakat [26] 2012 b Spain 83 40 43 3 Low–mod 28–33 w Land aerobic and aquatic activity Yes 35–45 min - Gestational weight
gain and gestational diabetes
Gestational age, type of delivery, birth weight
Barakat [27] 2013 Spain 510 255 255 3 Mod 28 w Aerobic, strength, and flexibility exercise Yes 50–55 min - Gestational diabetes, gestational age Gestational weight gain and birth weight
Barakat [28] 2014 a Spain 290 138 152 3 60–75% Max HR 28–31 w Aerobic exercise Yes 55–60 min 80% Gestational age Gestational diabetes, gestational weight gain
Barakat [29] 2014 b Spain 200 107 93 3 Mod 26–31 w Aerobic exercise Yes 55–60 min 80% Gestational age, gestational weight gain, type of delivery, gestational diabetes Birth weight, head circumference
Barakat [30] 2016 Spain 765 382 383 3 Mod 28 w Aerobic, strength, and flexibility exercise Yes 50–55 min 80% Hypertension Type of delivery, gestational age, birth weight
Barakat [31] 2018 a Spain 429 227 202 3 Mod 28 w Aerobic exercise Yes 55–60 min 80% Duration of labour, gestational age Type of delivery,
use of epidural, birth weight
Barakat [32] 2018 b Spain 65 33 32 3 Mod 28 w Aerobic, pelvic floor strength, and flexibility exercises Yes 55–60 min - Placenta’s weight Gestational age, type of delivery, birth weight
Barakat [33] 2019 Spain 456 234 222 3 Mod 28 w Aerobic exercise Yes 50–55 min - Gestational weight gain Gestational age, type of delivery, birth weight
Bhartia [34] 2019 India 78 38 40 1
2
Mod 12 w Yoga Yes
No
50 min - Maternal stress, type of delivery, birth weight Gestational age
Bjøntegaard [35] 2021 Norway 281 164 117 1–2 Mod–high 12 w Endurance, strength training and balance exercises Yes
No
60 min
45 min
- Type of delivery, birth weight, gestational age PA of children at age of seven
Brik [36] 2019 Spain 85 42 43 3 Light–mod 29 w Aerobic, strength, and pelvic floor exercises Yes 60 min 70% Gestational weight gain Type of delivery, birth weight, gestational age
Carrascosa [37] 2021 Spain 286 145 141 3–5 55–65% Max HR 20 w Water aerobic exercise Yes 45 min - Use of epidural analgesia during labour Type of delivery, time of active labour, episiotomy, gestational age
Clark [38] 2018 USA 36 14 22 3 Mod 20 w Aerobic Yes 60 min - Gestational weight gain, gestational age Type of delivery, birth weight
Cordero [39] 2012 Spain 55 25 30 3 50–55% Max HR 28–33 w Aerobic and strength training Yes 50 min 80% Gestational weight gain, gestational diabetes, Gestational age
Cordero [40] 2015 Spain 342 122 220 3 Mod 24 w Aerobics in a gym hall and aquatic activity Yes 50–60 min 80% Gestational diabetes, gestational age Gestational weight gain, type of delivery, birth weight
Da Silva [41] 2017 Brazil 639 213 426 3 Mod 16+ w Aerobic, strength and stretching training Yes 60 min 70% Gestational age, preterm birth, and pre-eclampsia Gestational weight gain, birth weight
Daly [42] 2017 Ireland 88 44 44 3 Mod 8 w Aerobic pelvic floor exercises Yes 50–60 min - Maternal fasting plasma glucose, gestational age Type of delivery
and birth weight
de Barros [43] 2010 Brazil 64 32 32 1–2 Mod 12 w Resistance exercise Yes
No
30 min - Gestational diabetes, gestational age -
Dias [44] 2011 Norway 42 21 21 1 Low 16 w Pelvic floor muscle training Yes 30 min 75% Type of delivery, birth weight, gestational age Pelvic floor muscle strength
Ellingsen [45] 2020 Norway 279 164 115 1–2 Mod 12 w Aerobic activity and strength exercises Yes
No
60 min
45 min
- Neurodevelopmental in 7-year-old children Gestational age, birth weight, type of delivery
Fernández-Buhigas [46] 2020 Spain 92 41 51 3 50–60% Max HR 23–27 w Aerobic, strength, coordination and balance, pelvic floor exercises Yes 60 min 80% Blood pressure, gestational weight gain Gestational age
Ghodsi [47] 2014 Iran 80 40 40 3 50–60% Max HR 12–18 w Stationary cycling No 15 min - Gestational age, type of delivery, perineal tear -
Guelfi [48] 2016 Australia 169 84 85 3 65–75% Max HR 14 w Home-based stationary cycling program Yes 60 min - Gestational diabetes Gestational age, type of delivery, birth weight
Haakstad [49] 2011 Norway 105 52 53 2–1 Mod 12 w Aerobic dance and strength training Yes
No
60 min
30 min
- Birth weight Gestational age, type of delivery
Halse [50] 2015 Australia 40 20 20 3 55–65% Max HR 6 w Stationary cycling No 45 min - Maternal attitude and intentions of exercise Gestational age, gestational weight gain
Hellenes [51] 2015 Norway 336 188 148 1–3 Mod 16 w Aerobic activity Yes
No
30+ min - Cognitive, language and motor domains of children Gestational age, birth weight, and type of delivery
Kong [52] 2014 USA 37 18 19 5 Mod 20 w Treadmill walking No 30 min - Postpartum weight retention Gestational weight gain, gestational age, birth weight
Leão [53] 2022 Brazil 424 141 283 3 Mod 16 w Aerobic and strength training Yes 60 min 70% Childhood neurodevelopment Gestational age
McDonald [54] 2021 USA 192 131 61 3 Mod 24+ w Aerobic and resistance training Yes 50 min - Infant Morphometry Gestational age
McMillan [55] 2019 USA 60 33 27 3 Mod 20 w Aerobic activity Yes 50 min Infant neuromotor skills Gestational weight gain, gestational age
Murtezani [56] 2014 Repub. of Kosovo 63 30 33 3 Mod 20 w Aerobic and strength exercises Yes 40–45 min - Birth weight, gestational age -
Nascimento [57] 2011 Brazil 82 40 42 1–5 Low–mod 22 w Aerobic exercise,
walking
Yes
No
40 min - Gestational weight gain, gestational age Birth weight
Nobles [58] 2015 USA 251 124 127 5 Mod 12 w Aerobic activity No 30 min - Gestational diabetes Birth weight, gestational age
Pais [59] 2021 India 132 66 66 7 Low 14–18 w Yoga No 45 min - Preeclampsia and gestational diabetes Gestational age, analgesia, duration of labour, type of delivery, birth weight
Perales [60] 2015 Spain 63 38 25 3 55–60% Max HR 26–31 w Aerobic dance, pelvic floor muscle training Yes 55–60 min - Foetal and maternal heart rate Gestational weight gain, gestational age, birth weight, type of delivery
Perales [61] 2016 Spain 166 83 83 3 55–60% Max HR 28–31 w Aerobic and strength exercises Yes 55–60 min - Duration of labour, gestational age, type of delivery, birth weight -
Perales [62] 2020 Spain 1348 668 660 3 Light–mod 30 w Aerobic, pelvic floor exercises Yes 50–55 min - Gestational weight gain, hypertension and gestational diabetes Type of delivery, birth weight, gestational age, preterm delivery
Raper [63] 2021 USA 125 58 67 3 Mod 22 w Aerobic Yes 50 min 80% Gestational diabetes, type of delivery and birth weight Gestational age
Renault [64] 2014 Denmark 283 142 141 7 Low 22–26 w 11,000 daily steps No 60+ min - Gestational weight gain, miscarriage Gestational age
Ruchat [65] 2012 Canada 71 26 45 2–3 Mod 22 w Walking Yes
No
25–40 min - Gestational weight gain, birth weight, gestational age -
Ruiz [66] 2013 Spain 96 48 48 3 Light–mod 29–30 w Aerobic and resistance exercises Yes 50–55 min - Gestational weight gain, gestational age Birth weight, type of delivery
Sagedal [67] 2017 Norway 591 296 295 2 Mod 24 w Strength training and cardiovascular exercise Yes 60 min - Gestational weight gain, birth weight Gestational age
Sanda [68] 2018 Norway 589 295 294 2–3 Mod 22 w Aerobic exercises Yes
No
60 min
30 min
- Gestational age, duration of labour, type of delivery -
Seneviratne [69] 2015 New Zealand 75 38 37 3–5 Mod 16 w Stationary cycling program No 15–30 min - Birth weight, type of delivery Gestational weight gain, gestational age
Silva-Jose [70] 2022 Spain 157 78 79 3 Mod 28–31 w Aerobic exercise Yes 55–60 min 80% Gestational weight gain, gestational age Type of delivery, birth weight
Stafne [71] 2012 Norway 761 396 365 1–3 Mod 12 w Aerobics, strength, pelvic floor exercises Yes
No
60 min
45 min
- Urinary and anal
incontinence
Type of delivery, birth weight, gestational age
Taniguchi [72] 2016 Japan 118 60 58 3 Mod 6+ w Walk briskly Yes 30 min 80% Type of delivery, birth weight Gestational age
Tomic [73] 2013 Croatia 334 166 168 3 60–75% Max HR 28–30 w Aerobic exercise Yes 50 min 80% Macrosomia, birth weight, type of delivery, gestational weight gain Gestational age
Uria-Minguito [74] 2022 Spain 203 102 101 3 65–70% Max HR 28–31 w Aerobic exercise Yes 50–60 min - Gestational diabetes, gestational age Gestational weight gain, type of delivery, birth weight
Ussher [75] 2015 UK 789 394 395 3–4 Low 6 w Exercise on
treadmill
Yes 20 min - Continuous smoking abstinence Type of delivery, birth weight
Wang [76] 2017 China 300 150 150 3 55–65% Max HR 18 w Stationary cycling program Yes 60 min 75% Gestational diabetes Birth weight, macrosomia, gestational age
Yekefallah [77] 2021 Iran 70 35 35 2 Low–mod 11 w Yoga Yes 75 min - Episiotomy, type of delivery Birth weight, gestational age, duration of labour

Author last name (Ref). Year: year of study. Country: country where the article has been developed (usually in the method part). Type: type of article; if it is a randomized clinical (or controlled) trial, put RCT; if not, please specify the item. N: total number of women analysed. Those of the GI and those of the CG have to coincide. GI: number of women analysed in the intervention group. GC: number of women analysed in the control group. Freq: weekly frequency of exercise sessions (3 days a week, 2, etc.). Intens: type of intensity, e.g., moderate, high… Tp: program time; if the program has lasted 10 weeks, or if it has started in week 12 and ends in week 28, put it as 16 weeks long. Type: type of exercise performed, e.g., aerobic, muscle strengthening, etc. Superv. classes: whether or not there was supervision. Duration: minutes of each session. Adh.: adherence of the participants to the intervention (%); it is how and how many sessions women have attended. Main variables analysed: lists all the main variables of the study. It is usually in the method section in “outcomes”, and they appear as “main outcomes”. If main variables do not appear, they are the first. One can find it in several places. Secondary variables: the same as before but secondary.

3. Results

In total, 276 articles were retrieved in the first stage of the search, 184 of which were excluded because they did not meet the inclusion criteria (Figure 1). Then, 35 articles were excluded since they were a narrative review (n = 8), a pilot study (n = 5), they did not describe the intervention protocol (n = 12), or they did not provide information regarding gestational age (n = 10). Finally, 57 studies were included in the analysis.

For the first meta-analysis, all the selected studies were included that reported gestational age (Figure 2). On the other hand, 34 of them were represented in the second meta-analysis (Figure 3). In this group, studies reporting whether the women had had a preterm delivery were included.

Figure 2.

Figure 2

Effect of PA during pregnancy on gestational age [21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,44,45,46,48,49,50,51,53,55,56,57,58,59,60,61,62,63,65,66,68,69,70,71,72,73,74,75,76,77].

Figure 3.

Figure 3

Effect of PA during pregnancy on the ratio of preterm deliveries [22,23,26,28,29,30,32,34,35,36,41,42,43,47,48,49,50,52,53,54,58,59,62,64,66,67,68,69,70,72,73,75,76,77].

Regarding the type of intervention reported in the included studies (as shown in Table 1), most of them described PA sessions conducted by professionals in the field. The intervention consisted of aerobic exercise, strength exercises, or aquatic activities among others. The sessions in the studies included in the review were designed for moderate intensity and performed with a frequency of one to seven days per week, with a time duration between 15 and 75 min. The duration of each intervention oscillated between 2 and 24 weeks.

In terms of the quality of evidence assessed using the GRADE (Grading of Recommendations Assessment, Development, and Evaluation) approach, a total of 52 randomized controlled trials (RCTs) were analysed for the assessment of gestational age. The findings of these trials resulted in a classification of a “moderate” certainty and “critical” importance. Similarly, for the analysis of preterm delivery, 34 RCTs were evaluated, which provided a classification of a “high” certainty and “critical” importance.

3.1. Effect of PA on Gestational Age

Fifty-two different studies were included in this analysis, comparing gestational age between women in the experimental and control groups. The results revealed there was no significant association between exercise practice during pregnancy and gestational age (Z = 0.45, p = 0.65; ES = 0.08; 95% CI = −0.01 [−0.06–0.04]; and the values for heterogeneity analysis were Chi250 = 86.04 (p = 0.001), I2 = 42%). Figure 2 shows the forest plot corresponding to the present meta-analysis.

3.2. Effect of PA on the Risk of Preterm Delivery

Thirty-four studies were included in this analysis comparing the difference in the ratio of preterm deliveries between the experimental and control groups. The results revealed that there was no association between PA practice during pregnancy and preterm delivery risk. Specifically, the total compensated RR was 0.96 (95% CI = 0.77–1.21, Z = 0.33, p = 0.74: ES = 0.07), and the values for heterogeneity analysis were Chi233 = 47.49 (p = 0.05), I2 = 31%). These outcomes indicate that women who exercised during pregnancy did not present a significantly greater probability of experiencing preterm delivery. Figure 3 shows the forest plot corresponding to the present meta-analysis.

3.3. Risk of Bias Assessment

Overall, the risk of bias of each article was rated as low, unclear, or as a high potential risk (Figure 4). Reviewing the sources of bias, the articles showed mostly a low risk of bias on selection, detection, and attrition bias. Nearly a half of the studies (n = 27) presented an unclear performance risk. In this type of research (controlled trials), blinding participants is practically impossible. On the other hand, a high (n = 5) or unclear (n = 12) selection bias was reported for some studies due to the difficulty to access each protocol. Despite the high percentage of unclear risk of bias findings in the performance source, we followed Cochrane’s tool considering the difficulty in these types of studies when it comes to blinding participants [20]. Despite the high risk of bias scored in the reporting source, the outcomes of interest of each article (even the inaccessibility of their protocols) could not be related to gestational age or preterm delivery. The summary of the risk of bias assessment per study is included as Supplementary Materials (File S1).

Figure 4.

Figure 4

Risk of bias.

4. Discussion

The objective of the present systematic review and meta-analysis was to investigate the impact of PA during pregnancy on gestational age and the occurrence of preterm delivery. By assessing the potential risks to maternal and foetal well-being associated with an integral component of a pregnant woman’s daily life, namely PA, we aimed to enhance our understanding of its influence.

Our findings indicated that there were no adverse effects observed on both gestational age and the occurrence of preterm delivery. In fact, the exercise groups demonstrated a lengthened gestational age compared to the control groups, which is consistent with findings from other studies [11]. This is particularly significant because traditionally, a major concern surrounding exercise during pregnancy has been the potential for a decreased gestational age and increased risk of preterm delivery. However, our results support the recommendation of moderate PA throughout pregnancy for pregnant women without obstetric contraindications, aligning with a substantial body of literature [78,79,80].

From an epidemiological standpoint, when examining the underlying causes of the beneficial impact of physical exercise on gestational age, we encountered ample evidence to support a causal association between unhealthy lifestyles—such as excessive maternal weight gain, obesity, and smoking—and the occurrence of preterm delivery [81,82,83].

These findings lead us to propose the concept of a comprehensive preventive effect of PA throughout pregnancy, mitigating the risk factors associated with reduced gestational age and preterm birth. This notion is supported by other studies demonstrating the potential of PA to positively impact not only physiological aspects but also mental and emotional aspects, and the overall quality of life in pregnant women [84,85].

The results of this study further validate the current recommendations of engaging in 150 min of moderate PA per week throughout pregnancy for women without obstetric contraindications [79].

While no significant limitations of the evidence or the review processes used in the current study were identified, there are two minor limitations worthy of note. The first one refers to the diversity of interventions involving PA across the included studies; the absence of standardized protocols hampers the potential of meta-analyses to their fullest extent. On the other hand, the review included both women who exercised before and women who started exercising during pregnancy. However, we believe that this variability is inherent in the nature of the intervention itself.

5. Conclusions

PA during pregnancy does not contribute to adverse outcomes in terms of gestational age or increase the risk of preterm delivery among healthy pregnant women.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcm12154915/s1, File S1. Risk of bias; File S2. PRISMA 2020 Checklist.

Author Contributions

R.B. and E.F.; methodology, D.Z.; software, M.S.-P.; validation, D.Z., M.S.-P. and C.S.-J.; formal analysis, J.G.-A.; data curation, R.B. and E.F.; writing—original draft preparation, writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This research received no external funding.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

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