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Journal of Clinical Medicine logoLink to Journal of Clinical Medicine
. 2023 Aug 21;12(16):5421. doi: 10.3390/jcm12165421

Influence of Physical Activity during Pregnancy on Birth Weight: Systematic Review and Meta-Analysis of Randomized Controlled Trials

Dingfeng Zhang 1, Taniya S Nagpal 2, Cristina Silva-José 1, Miguel Sánchez-Polán 1, Javier Gil-Ares 1,*, Rubén Barakat 1
Editor: Eyal Sheiner
PMCID: PMC10455907  PMID: 37629463

Abstract

Birth weight is a marker that is often referred to determine newborn health, potential growth trajectories and risk of future disease. Accordingly, interventions to promote appropriate and healthy birth weight have been extensively studied and implemented in pregnancy. In particular, physical activity in pregnancy is recommended to promote appropriate fetal development and newborn birth weight. This systematic review and meta-analyses aimed to summarize the effect of physical activity during pregnancy specifically from randomized controlled trials on the following outcomes: birth weight, macrosomia, low birth weight, being large for the gestational age, and being small for the gestational age (Registration No.: CRD42022370729). 63 studies (16,524 pregnant women) were included. There was a significant negative relationship between physical activity during pregnancy and macrosomia (z = 2.16; p = 0.03; RR = 0.79, 95% CI = 0.63, 0.98, I2 = 29%, Pheterogeneity = 0.09). No other significant relationships were found. Promoting physical activity during pregnancy may be an opportune time to reduce the risk of future chronic disease, such as obesity, through the prevention of macrosomia and the promotion of appropriate birth weights.

Keywords: birth weight, macrosomia, low birth weight, gestational age, pregnancy, physical activity

1. Introduction

Birth weight is an important and accessible factor to evaluate newborn health and predict growth trajectories and downstream risk of potential chronic disease such as obesity [1]. The World Health Organization defines low birth weight as the weight of a newborn below 2500 g, typically representing the 10th percentile for its gestational age [2]. Newborns that are small for their gestational age (less than the 10th percentile based on gestational age) are at greater risk of having a low birth weight, and associations have also been found with long-term cognitive deficits in childhood and adolescence [3,4]. On the opposite end of the weight spectrum, macrosomia is defined arbitrarily as a birth weight exceeding 4000 g [5]. Babies born with macrosomia have a higher likelihood of encountering adverse delivery outcomes, including shoulder dystocia, brachial plexus injury, clavicular fracture, birth asphyxia, and neonatal mortality [6,7,8]. Moreover, macrosomia increases the risk of undergoing cesarean section and experiencing vaginal and perineal trauma, as well as postpartum hemorrhage [9,10]. Similar complications are associated with newborns that are large for their gestational age (within the 90th percentile based on their gestational age), including prolonged delivery and the risk of injury at birth. Given the risk of complications at either end of the birth weight spectrum, interventions to promote appropriate birth weight are integral.

Physical activity during pregnancy has been described as a modifiable and accessible health behavior to facilitate maternal and newborn health, including the promotion of an appropriate birth weight [11]. International guidelines for prenatal physical activity suggest that all pregnant individuals without contraindications for being active should aim to accumulate 150 min of moderate-intensity activity per week [12]. Contrary to popular social beliefs that physical activity in pregnancy could result in reduced fetal growth and development, no associations have been found with such factors [13]. In fact, being active throughout pregnancy has been shown to advance placenta blood perfusion [14], which can improve nutrient transport and overall placental function and therefore facilitate fetal development [15]. Furthermore, previous reviews have consistently advised that physical activity in pregnancy does not have adverse effects on fetal development [14,16,17].

However, associations between physical activity in pregnancy and birth weight have been inconclusive. For example, a recent systematic review of 32 studies on prenatal physical activity concluded that there is no association between engagement in physical activity throughout pregnancy and newborn body composition markers [18]. Another study that included objective measures of prenatal physical activity via accelerometry suggested that physical activity was correlated with birth weight, and specifically, that aerobic activity reduced birth weight and increased the number of newborns weighing within the appropriate range [19]. Contrarily, a recent meta-analysis of randomized controlled trials that included studies that had assessed gestational weight gain found no associations between prenatal physical activity and large- or small-for-gestational-age newborns [20]. Despite the inconsistencies in the literature regarding birth weight, prenatal physical activity is still recommended, given the several health benefits for both the pregnant person and future child [16]. In fact, a recent expert review emphasized that physical activity in pregnancy should be integrated into standard care, especially given the high quality and strong evidence base supporting its contribution to reduced perinatal complications and improved labor and delivery outcomes [16].

Rather than negating or minimizing the potential benefits of prenatal physical activity on birth weight due to inconsistent results, they indicate that it may be necessary to further examine this relationship via high-quality randomized controlled trials that specifically target these outcomes. Accordingly, the purpose of this systematic review and meta-analysis was to assess the effect of prenatal physical activity on markers of birth weight (i.e., total birth weight and incidences of being large for the gestational age, being small for the gestational age, low birth weight, and macrosomia) from randomized controlled trials. We hypothesized that the amalgamated findings from randomized controlled trials would be in favor of physical activity in pregnancy for reduced risk of being large for the gestational age, being small for the gestational age, having a low birth weight, and macrosomia, along with showing a significant association with reduced total birth weight.

2. Methods

A systematic review was developed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) [21]. The protocol was registered in the International Prospective Registry of Systematic Reviews (PROSPERO), Registration No. CRD42022370729.

2.1. Eligibility Criteria

The eligibility criteria for this systematic review and meta-analysis was guided by the PICOS framework: participants, interventions, comparisons, outcomes, and study design [20]. The participants included pregnant women, the intervention was physical activity, the comparison was no physical activity/control, and the outcomes were birth weight, being small for the gestational age, being large for the gestational age, and macrosomia.

2.2. Population

The population of interest was pregnant individuals without contraindication to exercise or physical activity (following the most recent international clinical guideline about physical activity during pregnancy) [22,23]. Absolute contraindications were characterized by conditions such as ruptured membranes, premature labor, persistent second- or third-trimester bleeding, and other similar factors. On the other hand, relative contraindications were characterized by a history of spontaneous abortion, mild/moderate cardiovascular or respiratory disease, etc. [22,23].

2.3. Intervention (Exposure)

We conducted a search to identify physical activity interventions during pregnancy that involved quantifiable forms of physical activity. The focus was on extracting information regarding the program’s reporting of duration, intensity, type of activities, weekly frequency, session duration, participant adherence, and whether supervision was provided.

2.4. Comparison

The comparator was no exercise or physical activity (i.e., the control group of the selected studies), normally involving pregnant participants who followed a regular obstetrical follow-up in their health centers.

3. Outcome

The main outcomes of the study were birth weight, macrosomia, and low birth weight. Secondary outcomes were being large for the gestational age and being small for the gestational age.

4. Data Sources

A comprehensive search was carried out through the Universidad Politécnica de Madrid software in the following databases: Academic Search Premier, ERIC, MEDLINE, SPORTDiscus, OpenDissertations, Clinicaltrials.gov, Web of Science, Scopus, the Cochrane Database of Systematic Reviews, and the Physiotherapy Evidence Database (PEDro). To ensure equality in the selection process, the same article selection criteria were used for all databases, considering differences in controlled vocabulary and rules of selection syntax. The search terms used were:

  • English: (physical activity OR exercise OR training OR physical exercise OR fitness OR (strength training) OR physical intervention OR Pilates OR Yoga OR strengthening OR aerobic OR resistance training OR pelvic floor muscle training) AND (pregnancy OR maternal OR antenatal OR pregnant AND (birth weight OR macrosomia OR low birth weight OR large gestational age OR small gestational age) AND (randomized clinical trial OR randomized controlled trial OR RCT).

  • Spanish: (actividad física O ejercicio O entrenamiento O ejercicio físico O fitness O entrenamiento de fuerza O intervención de actividad física O Pilates O Yoga O fortalecimiento O aeróbico O entrenamiento de resistencia O fortalecimiento del suelo pélvico) Y (embarazo O materno O antenatal O embarazada Y peso de nacimiento O macrosomía O bajo peso al nacer O gran edad gestacional O pequeña edad gestacional) Y (ensayo clínico aleatorizado O ensayo controlado aleatorizado O ECA).

5. Study Selection and Data Extraction

Only randomized controlled trials (RCTs) were selected. Also, systematic reviews previously published in the same field were searched to compare our results. Articles published between 2010 and 2023 written in English and Spanish were considered for the search. Reference lists of selected studies were retrieved to identify other studies that might have been missed by the electronic keyword search.

To ensure compliance with the inclusion criteria, two reviewers (MS and CS) conducted an independent screening of the titles and abstracts retrieved from the electronic searches. The abstracts that met the initial screening were subjected to further analysis. The full texts were screened independently by two reviewers (JG and RB) to identify outcomes of interest for data extraction.

To identify any potential additional studies that were not captured by the electronic searches, the list of references from selected articles was screened. In cases where a study had multiple publications, the most recent or comprehensive publication was chosen as the primary source. However, relevant data from all the publications were extracted to ensure that no valuable information was overlooked.

For studies where one reviewer (DZ) recommended exclusion, both reviewers (CS and MS) tried to reach a consensus to make a final decision for exclusion or inclusion. In situations of absolute discrepancy, a third reviewer (RB) provided their expert opinion on whether the study should be included or excluded. The study selection process is detailed in Figure 1.

Figure 1.

Figure 1

Flow chart of the retrieved and analyzed articles.

Data extraction tables were created in an Excel sheet. One researcher extracted the data, and then data extraction was independently verified by a content expert to facilitate further analysis. Extracted data were study characteristics (i.e., author last name, year and country), type of article (RCT), total sample size and group sample size, intervention/exposure (exercise prescribed and/or measured), including: frequency, intensity, time and type, supervision of intervention, duration of intervention and adherence of intervention, primary and secondary outcomes (Table 1).

Table 1.

Characteristics of the studies analyzed.

Author Year Country Type N EG CG Intervention Physical Exercise Program Main Variables Analyzed Secondary Variables Analyzed
Freq Intensity Duration of Program Type of Exercise Superv. Class Duration of Class Adh.
Aktan [24] 2021 Turkey RCT 43 21 22 2 Mod 8 w Clinical Pilates exercise Yes 60 min - General anxiety, gestational weight gain Type of delivery, birth weight
Atkinson [25] 2022 Canada RTC 241 119 122 3–4 Mod 22 w Walking No 25–40 min 80% Gestational weight gain Depression, type of delivery, and birth weight
Babbar [26] 2016 USA RCT 46 23 23 3 Mod 8 w Yoga Yes 60 min 80% Umbilical artery, type of delivery, birth weight Gestational weight gain
Bacchi [27] 2018 Argentina RTC 111 49 62 3 Low–Mod 28 w Aquatic activities Yes 55–60 min 80% Gestational weight gain and birth weight -
Backhausen [28] 2017 Denmark RCT 516 258 258 2 Low 12 w Water exercise No 70 min 76% Low back pain, birth weight Type of delivery
Barakat [29] 2012 Spain RCT 290 138 152 3 Mod 28 w Aerobic exercise Yes 40–45 min - Type of delivery Gestational weight gain and birth weight
Barakat [30] 2013 Spain RCT 510 255 255 3 Mod 28 w Aerobic, strength, and flexibility exercise Yes 50–55 min 95% Gestational diabetes Gestational weight gain and birth weight
Barakat [31] 2016 Spain RCT 765 382 383 3 Mod 28 w Aerobic, strength, and flexibility exercise Yes 50–55 min 80% Hypertension Type of delivery, gestational weight gain, birth weight
Barakat [32] 2018a Spain RCT 429 227 202 3 Mod 28 w Aerobic exercise Yes 55–60 min 80% Duration of labor Type of delivery,
use of epidural, birth weight
Barakat [33] 2018b Spain RCT 65 33 32 3 Mod 28 w Aerobic, pelvic floor strength, and flexibility exercise Yes 55–60 min 85% Placenta weight Gestational age, type of delivery, birth weight
Barakat [34] 2018c Spain RCT 456 234 222 3 Mod 28 w Aerobic exercise Yes 50–55 min 80% Gestational weight gain Gestational age, type of delivery, birth weight
Bhartia [35] 2019 India RCT 78 38 40 1 Mod 12 w Yoga Yes 50 min - Maternal stress, type of delivery, birth weight -
2 No
Bjøntegaard [36] 2021 Norway RCT 281 164 117 1 Mod 12 w Aerobic, strength, and balance exercise Yes 60 min - Type of delivery, birth weight Physical activity of children at age of seven
2 No 45 min
Brik [37] 2019 Spain RTC 85 42 43 3 55–60% Max HR 29 w Aerobic, strength, coordination and balance, and pelvic floor exercise Yes 60 min 70% Gestational weight gain, fetal cardiac function Type of delivery, birth weight, gestational age
Bruno [38] 2016 Italy RTC 131 69 62 3 Mod 16 w Walking, dietary counselling No 30 min - Gestational diabetes Gestational weight gain, type of delivery, birth weight
Clark [39] 2018 USA RTC 36 14 22 3 Mod 20 w Aerobic Yes 60 min - Gestational weight gain Type of delivery, birth weight
Cordero [40] 2015 Spain RCT 257 101 156 2 50–55% Max HR 26 w Aerobics in gym hall Yes 50–60 min 80% Gestational diabetes Gestational weight gain, type of delivery, birth weight
1 Aquatic activity
Da Silva [41] 2017 Brazil RTC 639 213 426 3 Mod 16 w Aerobic, strength training Yes 60 min 70% Preterm birth and pre-eclampsia Gestational weight gain, birth weight
Daly [42] 2017 Ireland RCT 88 44 44 3 Mod 26 w Aerobic, pelvic floor exercise Yes 50–60 min 80% Maternal fasting plasma glucose Type of delivery
and birth weight
De Oliveria [43] 2012 Brazil RTC 111 54 57 3 60–80% Max HR 25 w Walking Yes 15–40 min 85% VO2max, birth weight and gestational age -
Ellingsen [44] 2020 Norway RTC 279 164 115 1 Mod 12 w Aerobic activity and strength exercise Yes 60 min - Neurodevelopment in 7-year-old children Gestational age, birth
weight, type of delivery
2 No 45 min
Fritel [45] 2015 France RCT 282 140 142 1 Low 8 w Pelvic floor training Yes 20–30 min - Urinary incontinence Type of delivery and birth weight
Garnaes [46] 2017 Norway RCT 74 38 36 3 Mod 20 w Aerobic, strength training Yes 60 min - Birth weight Type of delivery, perineal tears, gestational age
2 - No 50 min
7 Pelvic floor training No 1 min
Guelfi [47] 2016 Australia
RCT 172 85 87 3 Mod 14 w Home-based stationary cycling program Yes 20–60 min - Gestational diabetes Type of delivery, birth weight
Haakstad [48] 2011 Norway RCT 105 52 53 2 Mod 12 w Aerobic dance and strength training Yes 60 min 80% Birth weight Gestational age, type of delivery
1 No 30 min
Hellenes [49] 2015 Norway RCT 336 188 148 1 Mod 16 w Aerobic activity Yes 30 + min - Cognitive, language and motor domains of children Gestational age, birth weight, and type of delivery
2 No
Hopkins [50] 2010 New Zealand RCT 84 47 37 5 65%
VO2max
16 w Stationary cycling program No 40 min - Birth weight, gestational age -
Johannessen [51] 2021 Norway RCT 722 383 339 1 Mod 12 w Aerobic, strength and pelvic floor exercise Yes 55–70 min - Urinary incontinence at 3 months postpartum Type of delivery, episiotomy, epidural, duration of labor, birth weight
2 No 45 min
Karthiga [52] 2022 India RCT 234 121 113 7 Mod 20 w Yoga
5 sessions of Yoga techniques
No 60 min - Gestational hypertension Type of delivery, duration of labor, birth weight
Labonte-Leymoyne [53] 2017 Canada RCT 18 10 8 3 55%
VO2max
24 w Aerobic exercise Yes 20 + min - Neuroelectric response of the neonatal brain Maternal weight gain, birth weight
Leon-Larios [54] 2017 Spain RCT 466 254 212 5 Low 6 w Perineal massage and pelvic floor exercise No 18–23 min - Perineal tear and episiotomy Type of delivery, duration of labor, birth weight, and epidural analgesia
McDonald [55] 2018 USA RCT 90 49 41 5 55–69% Max HR 20 w Walking program No 40 min - Preeclampsia and pathophysiological progress of preeclampsia Gestational weight gain and birth weight
McDonald [56] 2022 USA RCT 192 131 61 3 Mod 24 w Aerobic and resistance training Yes 50 min 80% Gestational weight gain, type of delivery and birth weight -
Murtezani [57] 2014 Republic of Kosovo RCT 63 30 33 3 Mod 20 w Aerobic and strength exercise Yes 40–45 min 85% Birth weight and gestational age -
Nagpal [58] 2020 Canada RCT 40 23 17 3 Mild 11 w Walking program + nutrition Yes 25–40 min 80.2% Scoring women on meeting the intervention goals Gestational weight gain, birth weight, macrosomia, and low birth weight
Nascimento [59] 2011 Brazil RCT 80 39 41 5 Low–Mod 17 w Aerobic exercise
Walking
No 40 min 62.5% Gestational weight gain Birth weight
Navas [60] 2021 Spain RCT 294 148 146 3 55–65% Max HR 20 w Aquatic exercise Yes 45 min - Postpartum depression, quality of life, and quality of sleep Gestational age, birth weight
Pais [61] 2021 India RCT 124 61 63 7 Low 20 w Yoga
One-to-one Yoga session for 7 days
No 45 min - Preeclampsia and gestational diabetes Gestational age, duration of labor, type of delivery, birth weight
Perales [62] 2014 Spain RCT 167 90 77 3 55–60% Max HR 29 w Aerobic activity Yes 55–60 min - Prenatal depression Gestational weight gain, birth weight, and type of delivery
Perales [63] 2015 Spain RCT 63 38 25 3 55–60% Max HR 28 w Aerobic dance, pelvic floor muscle training Yes 55–60 min 80% Fetal and maternal heart rate Gestational weight gain, birth weight, type of delivery
Perales [64] 2020 Spain RCT 1348 688 660 3 Light–Mod 30 w Aerobic, pelvic floor exercise Yes 50–55 min 95% Gestational weight gain, hypertension, and gestational diabetes Type of delivery, birth weight, gestational age
Pereira [65] 2022 Portugal RCT 126 63 63 3 55–69% Max HR 3 w Walking Yes 30 min - Rate of labor induction Type of delivery, birth weight
Phelan [66] 2011 USA RCT 363 179 184 7 Low 26 w Walking No 30 min - Gestational weight gain Gestational hypertension, birth weight, and type of delivery
Price [67] 2012 USA RCT 62 31 31 4 Mod 23 w Aerobic exercise Yes 45–60 min - Birth weight Duration of labor, type of delivery
Prabhu [68] 2015 India RCT 105 52 53 2 Mod 12 w Aerobic dance Yes 45 min 80% Birth weight -
1 No 30 min
Raper [69] 2021 USA RCT 125 58 67 3 Mod 24 w Aerobic Yes 50 min 80% Gestational diabetes, type of delivery, and birth weight -
Rodriguez-Blanque [70] 2019 Spain RTC 129 65 64 3 Mod 17 w Aquatic physical exercise Yes 60 min - Laceration and episiotomy rates Type of delivery, birth weight, and anesthesia
Rodriguez-Diaz [71] 2017 Spain RCT 100 50 50 2 Mod 8 w Pilates Yes 40–45 min 90% Gestational weight gain, blood pressure, strength, flexibility, and spinal curvature Type of delivery, episiotomy, analgesia, and birth weight
Ruchat [72] 2012 Canada RCT 71 26 45 1 Mod 22 w Walking Yes 25–40 min - Gestational weight gain, birth weight -
2–3 No
Ruiz [73] 2013 Spain RCT 962 481 481 3 Light–Mod 28 w Aerobic and resistance exercise Yes 50–55 min 97% Gestational weight gain Birth weight, type of delivery
Sagedal [74] 2017 Norway RCT 591 296 295 2 Mod 24 w Aerobic, strength training. Dietary counselling Yes 60 min - Gestational weight gain, birth weight Gestational age, perineal tear
Seneviratne [75] 2015 New Zealand RCT 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 [76] 2022 Spain RCT 139 69 70 3 55–65% Max HR 30 w Aerobic exercise Yes 55–60 min 80% Gestational
weight gain
Birth weight, type of delivery
Sobhgol [77] 2022 Australia RCT 200 100 100 7 Low 16 w Pelvic floor muscle exercise No 30 min 50% Female sexual function Type of delivery, perineal tear, episiotomy, duration of labor, and birth weight
Stafne [78] 2012 Norway RCT 761 396 365 2 Mod–High 12 w Aerobic, strength, pelvic floor training Yes 60 min 55% Urinary and anal
incontinence
Type of delivery, birth weight
1 No 45 min
Szumilewicz [79] 2020 Poland RCT 260 133 127 3 Low–Mod 24 w Aerobic, resistance, pelvic floor muscle training Yes 60 min - Urinary incontinence 2 months and 1 year postpartum Type of delivery, birth weight, duration of labor, analgesia
Taniguchi [80] 2016 Japan RCT 118 60 58 3 Mod 6 + w Walk briskly Yes 30 min 80% Type of delivery, birth weight -
Tomic [81] 2013 Croatia RCT 334 166 168 3 60–75% Max HR 28 w Aerobic exercise Yes 50 min 80% Macrosomia, birth weight, type of delivery, gestational weight gain -
Uria-Minguito [82] 2022 Spain RCT 203 102 101 3 65–70% Max HR 28 w Aerobic exercise Yes 50–60 min - Gestational diabetes Gestational weight gain, type of delivery, birth weight
Ussher [83] 2015 UK RCT 789 394 395 3–4 Low 6 w Exercise on
a treadmill
Yes 20 min 88.8% Continuous smoking abstinence Type of delivery, birth weight
Vinter [84] 2011 Denmark RCT 304 150 154 7 Mod 24 w Aerobic exercise, dietary counselling No 30–60 min - Gestational weight gain Birth weight
Wang [85] 2017 China RCT 226 112 114 3 55–65% Max HR 24 w Stationary cycling program Yes 45–60 min 75% Gestational diabetes Birth weight, macrosomia
Yekefallah [86] 2021 Iran RCT 70 35 35 2 Low–Mod 11 w Yoga Yes 75 min - Episiotomy, perineal tear, type of delivery Birth weight, gestational age, duration of labor

Author: first author last name; Year: year of study; Country: country where the article was developed (usually in the method part); Type: type of article, if it is a randomized clinical (or controlled) trial, RCT is indicated. N: total number of women analyzed. Those of the GI and those of the CG have to coincide. EG: Number of women analyzed in the intervention group. CG: number of women analyzed in the control group. Freq: weekly frequency of exercise sessions (3 days a week, 2, etc.). Intensity: moderate, high...; Duration of program: program time. If the program lasted 10 weeks, or if it started in week 12 and ended in week 28, it is described as being 16 weeks long. Type of exercise: aerobic, muscle strengthening, etc. Superv. Classes: whether or not there was supervision. Duration of class: minutes of each session. Adh.: adherence of the participants to the intervention (%). This indicates how many women attended. Main variables analyzed: lists all the main variables of the study. This is usually in the method section in “outcomes”, and they appear as “main outcomes”. If main does not appear, they are the first. You will find it in several places. Secondary variables: the same as before, but secondary. In the same study, this may involve different types of exercises, varying durations for each exercise, and both supervised and unsupervised exercises.

6. Quality of Evidence and Risk of Bias Assessments

To evaluate the quality of evidence for each study design and outcome, the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework was used. This framework provides a standardized and comprehensive approach to assess the strength of the evidence across multiple studies [87].

To evaluate the risk of bias, the Cochrane Handbook was utilized. The potential sources of bias evaluated are selection bias (inadequate randomization procedures for RCTs), performances bias (compliance with the intervention for RCTs), detection bias (flawed outcome measurement), attrition bias (incomplete follow-up and high loss to follow-up), and reporting bias (selective or incomplete outcome reporting) [88].

7. Statistical Analysis

Statistical analyses were performed with the software RevMan in its 5.3 version. For continuous variables, birth weight (grams), mean, and standard deviations were recorded. The overall confidence interval (CI) was calculated using the mean difference (MD) [89]. All dichotomous outcomes, macrosomia, low birth weight, being large for the gestational age, and being small for the gestational age were expressed as categorical variables (Yes/No) to calculate the relative risk (RR) [90]. Random effect models were applied. To establish the compensated average in both dichotomous and continuous analyses, a weight system was used that considered the sample size per group, and, generally, these were contributed by each study. To assess the variation in study results between studies (i.e., the degree of heterogeneity), the I2 statistic was interpreted using established thresholds: 25% for low heterogeneity, 50% for moderate heterogeneity, and >75% for high heterogeneity [91].

8. Results

8.1. Study Characteristics

In total, 63 studies that met the inclusion criteria were identified, involving 16,524 pregnant women across 23 countries on five continents. All of the studies were randomized control trials, including 59 exercise interventions only and 4 of exercise and dietary counselling. Studies varied in frequency from 2 to 7 days per week, with low to moderate intensities lasting 15 to 75 min per session. These interventions were carried out during the first, second, and third trimesters, and lasted from 3 to 30 weeks. The types of exercise included walking, stationary cycling, water aerobics, swimming, resistance training, stretching, Pilates, Yoga, pelvic floor muscle training, and combinations of various exercise types. Additional details about the studies can be found in the Table 1. The results of mean birth weight, macrosomia, low birth weights, being large for the gestational age, and being small for the gestational age are presented below.

8.2. Risk of Bias Assessment

Collectively, the quality of evidence varied from low to high. In some situations, the blinding of participants to the group (intervention or control group) was not feasible, and it is typically impossible to achieve due to the intervention characteristics (physical activity intervention), resulting in unclear or high risk of bias (performance bias), depending on how it was recorded. Other sources of bias in some cases were the impossibility of finding the published article protocol (to compare the planned and measured outcomes), but also a lack of reporting (or having an uncertain definition) of the randomization process. Overall, the majority of the studies presented a low risk of bias within the five types of bias assessed. The risk of bias analysis is reported in Figure 2.

Figure 2.

Figure 2

Risk of bias of the included studies [24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86].

8.3. Effect of Physical Activity during Pregnancy on Birth weight

There were a total of 61 studies that were incorporated in this analysis [24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,85,86]. Regular exercise or physical activity during pregnancy did not have a significant relationship with birth weight (z = 0.11; p = 0.91) (Std. Mean Dif., Random, 95% CI = 0.00 (−0.04, 0.05) I2 = 43%, Pheterogeneity = 0.0003). The forest plot corresponding to the current meta-analysis is illustrated in Figure 3.

Figure 3.

Figure 3

Effect of exercise during pregnancy on birth weight [24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86].

8.4. Effect of Physical Activity during Pregnancy on Macrosomia

This analysis included a total of 25 studies [27,30,31,32,33,34,38,40,41,42,43,46,48,55,57,58,66,67,72,73,75,76,78,84,85]. There was a significant relationship (z = 2.16; p = 0.03) between physical activity during pregnancy and macrosomia (RR = 0.79, 95% CI = 0.63, 0.98, I2 = 29%, Pheterogeneity = 0.09) such that macrosomia occurred less frequently in the exercise group. In Figure 4, the forest plot pertaining to the current meta-analysis is depicted. In addition, we tested only the studies that reported on macrosomia for differences in birth weight, and none were observed (z = 0.86; p = 0.39) (Figure 5).

Figure 4.

Figure 4

Effect of exercise during pregnancy on macrosomia [27,30,31,32,33,34,38,40,41,42,43,46,48,55,57,58,66,67,72,73,75,76,78,84,85].

Figure 5.

Figure 5

Effect of exercise during pregnancy on birth weight in studies reporting on macrosomia [27,30,31,32,33,38,40,41,42,43,46,48,55,57,58,66,72,73,75,78,84,85].

8.5. Effect of Physical Activity during Pregnancy on Low Birth Weight

This analysis comprised a total of 16 studies [27,31,33,40,41,42,48,52,57,66,69,72,73,75,76,83]. There was no statistically significant association (z = 1.25; p = 0.21) between physical activity during pregnancy and the likelihood of low birth weight (RR = 0.84, 95% CI = 0.65, 1.10, I2 = 9%, Pheterogeneity = 0.35). Figure 6 displays the forest plot for the present meta-analysis.

Figure 6.

Figure 6

Effect of exercise during pregnancy on low birth weight [27,31,33,40,41,42,48,52,57,66,69,72,73,75,76,83].

8.6. Effect of Physical Activity during Pregnancy on Large for Gestational Age

There was a total of 10 studies that were incorporated into this analysis [25,38,41,43,47,59,74,75,84,85]. There was no difference (z = 0.31; p = 0.76) between intervention and control for being large for the gestational age (RR = 0.95, 95% CI = 0.71, 1.29, I2 = 30%, Pheterogeneity = 0.17). Figure 7 visually presents the results of the meta-analysis through a forest plot.

Figure 7.

Figure 7

Effect of exercise during pregnancy on being large for gestational age [25,38,41,43,47,59,74,75,84,85].

8.7. Effect of Physical Activity during Pregnancy on Small for Gestational Age

There was a total of 10 studies that were incorporated into this analysis [25,35,38,41,43,47,59,74,75,85]. Incorporating regular exercise during pregnancy did not cause a significant difference (z = 0.11; p = 0.91) for being small for the gestational age (RR = 1.02, 95% CI = 0.73, 1.41, I2 = 0%, Pheterogeneity = 0.76). The meta-analysis results are visually presented in Figure 8 through a forest plot.

Figure 8.

Figure 8

Effect of exercise during pregnancy on being small for gestational age [25,35,38,41,43,47,59,74,75,85].

9. Discussion

This systematic review and meta-analysis demonstrated the positive effect of physical activity in pregnancy in reducing the risk of macrosomia by referring specifically to evidence from randomized controlled trials. No other significant associations were found with indices of birth weight, including birth weight as a continuous variable, risk of being small for the gestational age, and having a low birth weight. Birth weight is often used as an accessible marker of newborn health and as an assessment of potential growth trajectories and downstream risk of chronic disease [1,92]. Physical activity during pregnancy may be a key factor in promoting appropriate birth weight, especially contributing to the prevention of macrosomia, and therefore is an important behavior that will facilitate both maternal and child health.

The only significant finding in relation to prenatal physical activity and birth weight was the reduced odds of developing macrosomia. This finding is consistent with previous reviews that have shown reduced odds of macrosomia with physical activity in pregnancy [13,93]. In fact, one systematic review that conducted a sub-analysis of randomized controlled trials only found a 39% reduced risk of macrosomia [13], and our findings further underscored this, thus supporting the effectiveness of prenatal physical activity in the prevention of macrosomia. Macrosomia has shown strong associations with the risk of downstream childhood obesity, and there have been both physiological and environmental mechanisms that have been proposed [94,95]. For example, it is theorized that macrosomia can be a proxy measure for potential adipose tissue function, including overactivity and therefore excess energy storage that can increase the risk for later-life obesity [96]. Moreover, early food restriction practices have been associated with infants who are larger, potentially as an effort to bring their weight into expected trajectories; however, this may be a detriment to appetite regulation [97,98] later on in life. In line with the Developmental Origins of Health and Disease, uterine and early life environments can program downstream childhood obesity, and perhaps prenatal physical activity is a viable factor that can prevent this by reducing the risk of macrosomia [99]. Notably, we also tested if birth weight was different only amongst the studies that reported on macrosomia, and this was not significant. We postulate that this may be due to the fact that macrosomia is defined in absolute values as >4000 g, whereas birth weight is continuous. It may also be due to the heterogeneity amongst included studies in the measurement of weight, as well as the types of exercises performed. Similar findings have been noted about nutrition and exercise interventions in pregnancy, where favorable prevalence outcomes have been found, such as the prevention of excessive gestational weight gain and macrosomia, but no differences were found when weight was measured continuously between intervention and control groups [24,57,70].

This review did not find any significant relationship with prenatal physical activity and birth weight, large- or small-for-gestational-age newborns, and low birth weight. These null findings are consistent with previous systematic reviews, meta-analyses, and observational studies [13,17,93,100]. Previous research has suggested that the relationship between physical activity during pregnancy and birth weight may have an inverted U-shape, such that higher frequencies and intensities of activity may be associated with being small for the gestational age or low birth weight, whereas lower frequencies and intensities of activity could increase risk of being large for the gestational age or macrosomia [101]. Notably, though, engagement in regular moderate levels of physical activity does not increase the risk for small-for-gestational-age and low-birth-weight newborns [13]. Therefore, although our results found no relationship with the lower end of the weight spectrum, it should be highlighted that engagement in physical activity throughout pregnancy does not increase the risk for smaller newborns. A common misconception is that physical activity in pregnancy could be unsafe for fetal development, as energy reserves would be diverted from the placenta, or there is a risk of physical harm [102]. In order to improve knowledge on the safety of maternal physical activity, it is essential that public health messaging should debunk stereotypes or myths that suggest physical activity in pregnancy can deplete or divert energy reserves for fetal growth and development.

Physical activity throughout pregnancy elicits several benefits for maternal and newborn health, including the prevention of perinatal complications such as excessive gestational weight gain and gestational diabetes [103,104]. In the present review, we assessed the direct relationship between engagement in a physical activity intervention and markers of birth weight; however, it should be acknowledged that benefits pertaining to birth weight could be moderated by improvements in other markers of perinatal health. For example, gestational weight gain and birth weight are positively correlated, and therefore, preventing excessive gestational weight gain may also affect the reduction in birth weight [105]. Similarly, gestational diabetes increases the risk for large-for-gestational-age newborns [106]. Physical activity in pregnancy reduces the risk for excessive gestational weight gain by 32% and gestational diabetes by 38% [102,103], and accordingly, may be attributed to also improving newborn birth weight. Physical activity also improves labor and delivery outcomes, including the reduced risk of cesarean section, thus preventing potential complications associated with higher-birth-weight newborns [107]. Taken together, the benefits of physical activity extend beyond indices of weight and affect both the pregnant person and newborn.

Strengths of this review include the inclusion of both English and Spanish articles, expanding the scope of our search in comparison to previous reviews that were restricted to one language, and the inclusion specifically of randomized controlled trials, allowing for the assessment of the features of physical activity interventions that may not be captured through observational studies (e.g., frequency and type of activity). Moreover, randomized controlled trials are deemed to provide more high-quality evidence. However, these results should be interpreted with caution due to the inclusion of studies deemed to be of low quality, as well as the heterogeneity in the contents of the included interventions. Future research should aim to further extrapolate findings based on the intensity of the intervention and types of physical activity. Future comprehensive research should also expand on the inclusion of additional languages.

10. Conclusions

By referring to evidence from randomized controlled trials, this review identified that prenatal physical activity could reduce the risk for macrosomia. Prenatal physical activity did not have a significant effect on mean birth weight, small- or large-for-gestational-age newborns, or low birth weight. Importantly, though, prenatal physical activity does not also increase the risk for smaller newborns, and this is an important message that should be widely disseminated to debunk myths associated with reduced or diverted energy reserves for fetal growth and development with active pregnancies. Further research is needed to examine the effect of prenatal physical activity on birth weight, including specific recommended intensity and types of activity, and whether birth weight is moderated through the prevention of other perinatal complications by physical activity, such as excessive gestational weight gain and gestational diabetes.

Acknowledgments

The authors would like to thank Ane Uría-Minguito and Alejandro Barrera for their collaboration in the preparation of this study.

Author Contributions

Conceptualization R.B., J.G.-A. and M.S.-P.; methodology, T.S.N., C.S.-J., R.B. and M.S.-P.; software, J.G.-A.; validation, D.Z. and C.S.-J.; formal analysis, D.Z., T.S.N., C.S.-J., R.B. and M.S.-P.; investigation, D.Z., T.S.N. and M.S.-P.; resources, R.B.; data curation, J.G.-A.; writing—original draft preparation, D.Z., T.S.N. and M.S.-P.; writing—review and editing, D.Z., R.B. and M.S.-P.; visualization, J.G.-A.; supervision, M.S.-P.; project administration, R.B. and M.S.-P.; funding acquisition, R.B. 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. The APC was funded by Project UPM C2311580017. Instituto de las Mujeres. Ministerio de Igualdad de España.

Footnotes

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