Skip to main content
International Journal of Environmental Research and Public Health logoLink to International Journal of Environmental Research and Public Health
. 2020 Oct 29;17(21):7928. doi: 10.3390/ijerph17217928

Physical Activity Level during Pregnancy in South Africa: A Facility-Based Cross-Sectional Study

Uchenna Benedine Okafor 1,*, Daniel Ter Goon 2
PMCID: PMC7663401  PMID: 33137931

Abstract

Physical activity participation during pregnancy confers many maternal and foetal health benefits to the woman and her infant and is recommended by various health bodies and institutions. However, in South Africa, scant information exists about the physical activity status and its determinants among pregnant women. The aim of this study was to assess the physical activity level and associated factors among pregnant women. This cross-sectional study enrolled 1082 pregnant women attending public health facilities in Buffalo City Municipality, Eastern Cape, South Africa. Information on socio-demographic and maternal characteristics were obtained, and the Pregnancy Physical Activity Questionnaire was used to assess physical activity during pregnancy. Multiple logistic regression analyses were used to assess associations between physical activity and the predictor variables during pregnancy. Adjusted odds ratios with 95% confidence interval were applied to estimate factors associated with physical activity levels. Statistical significance was set at p < 0.05. Only 278 of the women (25.7%) met recommendations for prenatal activity (≥150 min moderate intensity exercise per week). The average time spent in moderate–vigorous physical activity was 151.6 min (95% CI: 147.2–156.0). Most of the women participated in light exercises with a mean of 65.9% (95% CI: 64.8–67.0), and 47.6% (95% CI: 46.3–48.9) participated in household activities. The majority of the women did not receive physical activity advice during prenatal care sessions (64.7%). Factors negatively associated with prenatal physical activity were lower age (<19 years) (adjusted odd ratio (AOR) = 0.3; CI: 0.16–0.76), semi-urban residence (AOR = 0.8; CI: 0.55–1.03), lower educational level (AOR = 0.5; CI: 0.20–0.71), unemployment (AOR = 0.5; CI: 0.29–0.77) and nulliparity (AOR = 0.6; CI: 0.28–1.31). However, prenatal physical activity was positively associated with starting physical activity in the first trimester (AOR = 1.9; CI: 1.06–3.31) compared to other trimesters. The findings of this study demonstrated low levels of physical activity during pregnancy in South Africa. The majority of women did not meet the recommendation of 150 min of moderate intensity activity per week. Light intensity and household activities were the most preferred form of activity. The factors affecting physical activity of women in this present study include lower age, semi-urban setting, low educational level, unemployment and nulliparity. In order to increase activity levels, future work should seek to improve knowledge, access and support for physical activity in pregnant women in South Africa. This should include education and advocacy regarding physical activity for professionals involved in maternal health provision.

Keywords: physical activity, pregnancy, determinants, South Africa

1. Introduction

The physical and psychological benefits of participation in regular physical activity during pregnancy are incontestably widely reported in the literature; they are also known to improve maternal health. As such, specialised bodies and institutions such as the American College of Obstetricians and Gynaecologists (ACOG) [1], the U.S. Department of Health and Human Services (US DHHS) [2], World Health Organization (WHO) [3], the Joint Canadian Society for Exercise Physiology (CSEP)/Society of Obstetricians and Gynaecologists of Canada (SOGC) [4], Royal Australian and New Zealand College of Obstetrics and Gynaecology (RANZCOG) [5], International Olympic Committee (IOC) [6], Department of Health & Social Care, UK [7], Sports Medicine Australia [8], and the American College of Sports Medicine (ACSM) [9] recommend and encourage women, without contraindication, to engage in moderate-intensity exercise for 150 min per week. Scientific evidence has proven the risks of physical activity during pregnancy are rare [1]. However, the rate of prenatal activity is reportedly low, both in developed [10,11,12] and developing countries [13,14,15,16,17,18]. Put differently, few women meet the authoritative guidelines of physical activity during pregnancy, perhaps, due to varying factors.

The reasons for participation in physical activity during pregnancy are multifactorial, linked to demographics, perceived risk, and obstetric care advice. For instance, studies have found older, married [13,19], lower socioeconomic status and with multiple children [16], low educational level [14], and higher income [14,20] women are less likely to be active during pregnancy. Maternal or clinical demographic variables positively associated with physical activity in pregnancy include parity [16,21], history of miscarriage [21,22], nausea [15], habitual exercise before pregnancy [23], and a higher body mass index (BMI) [24]. Despite no scientific evidence associated with adverse outcomes (e.g., preterm birth, low birth weight, miscarriage and perinatal mortality) during or following prenatal physical activity [25,26,27,28], seemingly, some pregnant women and obstetric care providers still hold doubts concerning the safety of prenatal physical activity. These findings from the literature suggest participation in physical activity during pregnancy is an interplay of multiple factors operating at different levels of the dichotomous pregnancy spectrum.

The reasons for non-participation and types of prenatal activity varied across studies and different geographical settings. Therefore, understanding the factors influencing physical activity participation in pregnancy is important to guide physical activity intervention programmes. However, unlike in other continents or regions, few data exist on prenatal physical activity in Africa, and more specifically, in South Africa. Relatedly, studies assessing the prevalence and factors associated with physical activity in South Africa have largely focused on specific subpopulations, such as children [29,30,31,32], rural populations [32,33], health professionals [34,35], and Black women [33,36], whilst few studies [37,38,39,40] are on a special population of pregnant women, with unique pregnancy-related physical, physiological, and psychosocial characteristics. Of the few studies, none utilise large samples, with heterogeneous populations, and these studies were confined to only two provinces. Notably, there have been hardly any studies undertaken to assess the level, types and intensity, and correlates of physical activity among pregnant women in the Eastern Cape Province, South Africa. This study was designed to assess the prevalence of physical activity among pregnant women attending primary health centres in Buffalo City Municipality, Eastern Cape, South Africa, and the associated factors of physical activity during pregnancy.

2. Methods

2.1. Study Design, Setting, and Participants

This was a cross-sectional descriptive study conducted among pregnant women in 12 primary health centres in Buffalo City Municipality, in the Eastern Cape Province, South Africa. Buffalo City Municipality is situated on the East Coast of the Eastern Cape Province. The details of the study setting have been described in a recent publication [41]. Briefly, the municipality is economically, one of the poorest provinces among the nine provinces in South Africa. The Buffalo City Metropolitan Municipality accounts for a total population of 884,000, or 12.2% of the total population in the Eastern Cape Province. In total, 460,000 (51.99%) of the total population are females and 424,000 (48.01%) males [42]. Buffalo City Municipality has two provincial Hospitals (Frere and Cecilia Makhiwane hospitals), and two district hospitals (Bhisho and Grey hospitals). There are five community health centres, 72 primary health clinics, and 12 mobile health services [42]. In addition, all the community health centres and primary health clinics offer antenatal healthcare services freely to all pregnant women regardless of their geographical residence, ethnic, and socio-economic background. The community and primary health facilities deliver antenatal care services every working day. Personal communication with a health facility manager revealed that, on average, the clinics register 5–6 new pregnant women who visit the primary health centres per day. Therefore, annually, an estimated 17,000 pregnant women visit the 12 selected primary health clinics for antenatal services.

2.2. Sample Size Determination and Sampling Procedure

We applied the Sarmah et al. [43] formulae for an infinite population to calculate the sample size at a confidence level of 95%, with the precision level of ±3%, and at a prevalence of physical activity or exercise during pregnancy of 50% (p = 0.5) as follows:

p = 0.5 and hence q = 1 − 0.5 = 0.5; e = 0.03; z = 1.96

So, n0 = (1.96)2 (0.5)(0.5)(0.3)2=1067=1067.

However, adding 10% non-response, the final sample size was 1215 women, to account for possible attrition and to protect against possible data loss.

We applied a two-stage sampling technique to select pregnant women, regardless of the gestation period. Firstly, using a simple random procedure, 12 antenatal primary health centres were selected to participate in the study and, secondly, participants who meet the inclusion criteria were conveniently selected because of cost and easy accessibility, since the study was conducted at the health facilities. Pregnant women were included in the study if 18 years or older, receiving antenatal care, having a single pregnancy (not multiple ones), and could read or understand the IsiXhosa, Afrikaans or English languages. Women with disabilities or reasons to cease exercise at the time of recruitment, such as “persistent excessive shortness of breath that does not resolve on rest, severe chest pain, regular and painful uterine contractions, vaginal bleeding, persistent loss of fluid from the vagina indicating rupture of the membranes, and persistent dizziness or faintness that does not resolve on rest” [44], were excluded. Detailed information about the recruitment of the participants is shown in Figure 1.

Figure 1.

Figure 1

Flow diagram of sample selection and participation.

2.3. Ethics

The University of Fort Hare Health Research Ethics Committee approved the study protocol (Ref#2019 = 06 = 009 = OkaforUB). In addition, permission was obtained from the Eastern Cape Department of Health and all the selected health facilities. Informed consent was obtained from the pregnant women prior to data collection.

2.4. Data Collection

Data collection was conducted between July to October 2019. To ensure the required sample size, data collection was carried out at each antenatal health clinic on pre-specified days, in a designated room allocated to the primary researcher by the health facility manager. All eligible pregnant women attending their antenatal care visits at selected health facilities during the study period were randomly approached to participate in the study, after signing an informed consent form.

2.5. Main Outcome Measure: Physical Activity

The Pregnant Physical Activity Questionnaire (PPAQ) [45] was used to assess the level, type and intensity of prenatal activity. The primary outcome measure was active and inactive participation of pregnant women in physical activity during pregnancy. The PPAQ is a validated and reliable tool, widely used across countries to measure prenatal physical activity [45,46,47]. The PPAQ is comprised of 32 physical activities, which include household and care-giving (13 activities), occupational (five activities), sports and exercise (eight activities), transportation (three activities), and inactivity (three activities). We solicited participants’ participation on these different activities, and the type, intensity, duration and frequency of physical activity recorded as hours and minutes per day. To maximise the accuracy and ensure completeness of information, the PPAQ was interviewer-administered to the participants at 12 selected primary health centres during their antenatal visit and took approximately 20 to 25 min. The Metabolic Equivalent Task (MET) of each activity was categorised as sedentary (<1.5 METs), low or light (1.5– ≤3.0 METs), moderate (3.0–6.0 METs), and vigorous intensity (>6.0 METs) [45].

2.6. Covariates and Other Measurements

We developed a structured questionnaire to solicit information on socio-demographic, obstetrics and lifestyle behaviours of the participants. As with the PPAQ, this aspect of the questionnaire was interviewer-administered to obtain information on age, residence, ethnicity, marital status, level of education, employment status, religion, family support, and behavioural and lifestyle characteristics, which include, current exposure to alcohol and smoking. We categorised women as ‘smokers’, if they reported smoking any number of cigarettes during pregnancy, ‘non-smokers’ (reported not smoking), ‘drinkers’, as those who reported any use of alcohol during pregnancy, and ‘non-drinkers’ (reported no-drinking). Other information included whether participants had had antepartum haemorrhage in their first trimester, perceived health condition in pregnancy (women were asked how they perceive their general health: very good, good, or bad), whether participants received prenatal physical activity advice from health professionals, and had engaged in physical activity before and during pregnancy.

We obtained information on parity, mode of pregnancy delivery, and pregravid body mass index from the antenatal records of the participants.

We adopted the Institute of Medicine (IOM) recommended BMI cut-off values to classify underweight (<18.5 kg/m2), normal weight (18.5–24.9 kg/m2), overweight (25.0–29.9 kg/m2), and obese (>30.0 kg/m2) [48].

2.7. Data Analysis

Descriptive statistics, including mean and standard deviation (SD), median and inter-quartile range (IQR) or as proportions was applied. The Centers for Disease Control and Prevention (CDC) recommendations was used to classify women as ‘inactive’ (reporting 0–149 min of exercise per week), and ‘active’ (reported 150 min or more of physical activity) based on the combined moderate–vigorous minutes per week [49]. We applied bivariate and multivariate analyses to assess the factors affecting physical activity behaviour during pregnancy. The Chi-square was used to determine the associations between the physical activity levels and socio-demographic, lifestyle and obstetric characteristics. All the covariates associated with physical activity (that is, age, area of residence, marital status, educational level, employment status, parity, family support, mode of pregnancy delivery, antepartum haemorrhage, pre-pregnancy BMI, employment status, lifestyle behaviours, and physical activity before and during pregnancy) were included in the models. The odds ratio (OR) and corresponding confidence interval (CI) of 95% were calculated. A multiple logistic regression, using automatic variable selection procedure was applied to determine the factors that predict physical activity levels. Automatic variable selection procedures are statistical tools for choosing the best subset of predictor variables for a given response variable. The significance level was set at p = 0.05. The Statistical Package for Social Sciences (SPSS) (Version 24.0, IBM SPSS, Chicago, IL, USA) was used to perform all statistical analyses.

3. Results

3.1. Socio-Demographic, Obstetrics and Lifestyle Characteristics of Participants

Of the 1215 pregnant women recruited, 42 participants did not meet the eligibility criteria, 26 declined to participate, and 65 had incomplete information on medical records data so were excluded. Finally, 1082 participants were included in the analysis.

The mean age of study participants was 27.0 ± 6.2 years. The majority of the participants were aged 19–34 years (812; 75.1%), residing in an urban setting (48.3%), black (86.4%), never married (66.3%), and had attained Grade 7–12 educational (74.2%). In addition, the majority of the participants were unemployed (67.7%), Christian (89.1) and received family support (77.4%) (Table 1).

Table 1.

Socio-demographic, obstetrics and lifestyle characteristics of participants.

Variables Frequency Percentage
Age (years)
<19 118 10.9
19–34 812 75.1
>34 152 14.0
Residential area
Rural 118 10.9
Semi-urban 441 40.8
Urban 523 48.3
Race
Black 935 86.4
Coloured 147 13.6
Marital status
Married 236 21.8
Never married 717 66.3
Cohabiting 129 11.9
Educational level
Primary 84 7.8
Secondary 803 74.2
Tertiary 195 18.0
Employment status
Unemployed 733 67.7
Employed 349 32.3
Religion
Christian 964 89.1
Other 118 10.9
Family support
Adequate 837 77.4
Moderate 223 20.6
No support 22 2.0
Parity
Nulliparous 517 47.8
Primiparous 322 29.8
Multiparous 243 22.4
Delivery mode
Vaginal 457 42.2
Caesarean section 87 8.1
Both 538 49.7
Antepartum haemorrhage
Yes 69 6.4
No 1013 93.6
Perceived health condition
Very Good 440 40.7
Good 631 58.3
Bad 11 1.0
Smoking status
Yes 90 8.3
No 992 91.7
Alcohol use
Yes 147 13.6
No 935 86.4
Pregravid body mass index (kg/m2)
Underweight (<18.5) 22 2.0
Normal weight (18.5–24.9) 917 84.8
Overweight (25.0–29.9) 143 13.2
Planned pregnancy
Yes 351 32.4
No 731 67.6
Physical activity advice
Yes 382 35.3
No 700 64.7
Physical activity before pregnancy
Yes 378 34.9
No 704 65.1
Physical activity timing
1st trimester 188 17.4
2nd trimester 114 10.5
3rd trimester 27 2.5
Never 753 69.6

Concerning the maternal-obstetric and lifestyle characteristics, most of the participants were nulliparous (47.8%), had no antepartum haemorrhage (93.6%); and had vaginal (42.2%) and both vaginal and Caesarean section (49.7%) deliveries. The majority of the participants perceived their health as being in good condition (59.3%); an overwhelming majority had no chronic illness (93.5%), did not smoke (91.7%), nor drink alcohol (86.4%), and had normal pregravid BMI (84.8%). Of the 1082 women, 731 (67.7%) affirmed their pregnancy was not planned. The majority of the women had not received physical activity advice (700; 64.7%). In addition, 704 (65.1%) did not participate in physical activity before pregnancy, and the majority of the women (753; 69.6%) never participated in physical activity in any of the trimesters.

3.2. Physical Type and Intensity Levels

The women’s physical activities were compared according to type and intensity of exercise (Table 2). Descriptive analysis of physical activity scores, as derived from the PPAQ scoring regarding the level of physical activity, showed the average time spent in moderate–vigorous physical activity was 151.6 min (95% CI: 147.2–156.0). The majority of the women did not engage in moderate–vigorous intensity physical activity (i.e., sport/exercise score from PPAQ), but were physically active in light activities including household/caregiving, occupational and transportation activities.

Table 2.

Physical activity levels during pregnancy (minutes).

Activity Category Mean LCL UCL Minimum Quartile 1 Median Quartile 3 Maximum
Total energy expenditure 151.6 147.2 156.0 22.3 100.0 138.9 191.1 546.2
Total light 128.7 124.3 133.1 8.2 74.2 114.0 166.3 541.8
Subdivision by intensity
Sedentary 22.9 21.9 24.0 0.0 7.4 18.9 31.9 88.2
Light 99.6 96.5 102.7 7.1 61.3 89.6 131.8 314.5
Moderate 28.3 25.9 30.7 0.0 2.5 12.2 37.6 378.0
Vigorous 0.8 0.6 1.0 0.0 0.0 0.0 0.8 40.5
Subdivision by type of activity
Household/caregiving 73.8 70.6 77.0 0.0 35.0 65.3 92.8 413.0
Occupational 25.1 23.2 27.1 0.0 1.8 10.5 44.8 308.0
Sport/exercise 2.6 2.3 2.9 0.0 0.0 0.8 3.2 65.7
Transportation 23.1 21.5 24.6 0.0 3.4 14.0 35.0 157.5
Inactivity 27.0 25.8 28.2 0.0 14.0 18.9 41.5 98.0

LCL = Lower confidence level; UCL = Upper confidence level.

Likewise, Table 3 presents the summary of the contribution of each physical activity level to the total score. The results show that, on average, light physical activity contributed most to the total activity. The participants rarely performed vigorous-intensity activities. Besides levels of activity, the contribution was also determined according to type of physical activity, namely, household, occupational, sport/exercise and transportation. Household activity contributed most to the total activity followed by occupational and transportation, while sport/exercise had the lowest contribution level. The rest is accounted for by physical inactivity.

Table 3.

Contribution of each type activity to the total activity score.

Activity Category Mean LCL UCL Minimum Quartile 1 Median Quartile 3 Maximum
Subdivision by intensity
Light 65.9 64.8 67.0 8.5 53.1 65.9 80.2 100.0
Moderate 15.8 14.8 16.7 0.0 1.6 10.9 27.0 74.2
Vigorous 0.5 0.4 0.6 0.0 0.0 0.0 0.4 19.9
Subdivision by type of activity
Household/caregiving 47.6 46.3 48.9 0.0 31.0 47.3 63.7 97.7
Occupational 16.0 15.0 17.0 0.0 1.2 9.2 28.5 78.7
Sport/exercise 1.7 1.5 1.9 0.0 0.0 0.6 2.1 31.2
Transportation 14.0 13.2 14.8 0.0 3.3 10.2 20.9 77.9
Inactivity 20.8 19.8 21.7 0.0 8.0 17.4 30.5 98.0

LCL = Lower confidence level; UCL = Upper confidence level.

3.3. Level of Physical Activity

Shown in Table 4 is the multivariate logistics regression analysis showing sociodemographic correlates of physical activity during pregnancy. The prevalence of moderate-intensity physical activity was 25.7% (278 out of 1082). The odds of exercise among women under 19 years of age was significantly lower than the odds of exercise among the over 34 years age group. Women aged 20–34 years were significantly less likely to exercise compared to women over 34 years age (Crude Odds Ratio (COR) = 0.1; CI: 0.07–0.21). Pregnant women who resided in semi-urban (COR = 0.5; CI: 0.41.0–0.69), were black (COR = 1.9; CI: 1.34–2.83), and married (COR = 2.5; CI: 1.63–3.81) were significantly more likely to be physically active. Unemployed women (COR = 0.3; CI: 0.26–0.45) had smaller odds of participating in physical activity during pregnancy.

Table 4.

Multivariate logistics regression model of physical activity on sociodemographic characteristics.

Variables Total
(n = 1082)
Active
(n = 278)
Inactive
(n = 804)
COR (95% CI) AOR (95% CI)
n (%) n (%) n (%)
Age (years)
<19 118 (10.9) 14 (11.9) 104 (88.1) 0.1 (0.07–0.21) * 0.3 (0.16–0.76) *
19–34 812 (75.1) 168 (20.7) 644 (79.3) 0.3 (0.22–0.42) * 0.9 (0.57–1.40)
>34 152 (14.0) 96 (63.2) 56 (36.8) 1
Residential area
Rural 118 (10.9) 60 (50.8) 58 (49.2) 1.4 (0.97–1.88) 1.2 (0.78–2.00)
Semi-urban 441 (40.8) 111 (25.2) 330 (74.8) 0.5 (0.41–0.69) * 0.8 (0.55–1.03) *
Urban 523 (48.3) 107 (20.5) 416 (79.5) 1
Race
Black 935 (86.4) 233 (24.9) 702 (75.1) 1.9 (1.34–2.83) * 1.2 (0.71–2.12)
Other 147 (13.6) 45 (30.6) 102 (69.4) 1
Marital status
Married 236 (21.8) 75 (31.8) 161 (68.2) 2.5 (1.63–3.81) * 1.4 (0.84–2.49)
Never married 717 (66.3) 160 (22.3) 557 (77.7) 1.0 (0.74–1.38) 1.3 (0.79–2.12)
Cohabiting 129 (11.9) 43 (33.3) 86 (66.7) 1
Educational level
Primary 84 (7.8) 29 (34.5) 55 (65.5) 0.5 (0.28–0.72) * 0.4 (0.20–0.71) *
Secondary 803 (74.2) 181 (22.5) 622 (77.5) 0.4 (0.31–0.57) * 0.7 (0.45–0.95) *
Tertiary 195 (18.0) 68 (34.9) 127 (65.1) 1
Unemployment status
Unemployed 733 (67.7) 171 (23.3) 562 (76.7) 0.3 (0.26–0.45) * 0.5 (0.29–0.77) *
Employed 349 (32.3) 107 (30.7) 242 (69.3) 1
Religion
Christian 964 (89.1) 234 (24.3) 730 (75.7) 1.4 (0.93–2.04) 0.9 (0.53–1.39)
Other 118 (10.9) 44 (37.3) 74 (62.7) 1
Family support
Adequate 837 (77.4) 212 (25.3) 625 (74.7) 0.4 (0.28–0.59) * 1.0 (0.37–2.71)
Moderate 223 (20.6) 57 (25.6) 166 (74.4) 0.2 (0.09–0.28) * 0.7 (0.25–1.92)
No support 22 (2.0) 9 (40.9) 13 (59.1) 1

COR = Crude Odds Ratio, AOR = Adjusted Odds Ratio, CI = Confidence Interval; * Statistically significant.

The obstetric and lifestyle correlates of physical activity during pregnancy (Table 5) indicate that nulliparous women who had vaginal and caesarean section, planned pregnancy, physical activity advice, physical activity before pregnancy, and practiced physical activity during first and second trimester, were significantly more likely to be active in moderate-intensity activity during pregnancy.

Table 5.

Multivariate logistics regression model of physical activity on obstetric and lifestyle characteristics.

Variables Total
(n = 1082)
Active
(n = 278)
Inactive
(n = 804)
COR (95% CI) AOR (95% CI)
n (%) n (%) n (%)
Parity
Nulliparous 517 (47.8) 98 (19.0) 419 (81.0) 0.3 (0.24–0.44) * 0.6 (0.28–1.31) *
Primiparous 322 (29.8) 102 (37.3) 220 (68.3) 0.8 (0.54–1.06) 0.7 (0.45–1.03)
Multiparous 243 (22.4) 78 (32.1) 165 (67.9) 1
Previous mode of delivery
Vaginal 457 (42.2) 127 (27.8) 330 (72.2) 2.4 (1.89–3.16) * 1.7 (0.86–3.54)
Caesarean section 87 (8.1) 52 (59.8) 35 (40.2) 3.3 (2.31–4.69) * 1.7 (0.72–3.82)
Both 538 (49.7) 99 (18.4) 439 (81.6) 1
Antepartum haemorrhage
Yes 69 (6.4) 33 (47.8) 36 (52.2) 1.2 (0.72–1.91) 1.2 (0.66–2.05)
No 1013 (93.6) 245 (24.2) 768 (75.8) 1
Perceived health condition
Very Good 440 (40.7) 87 (19.8) 353 (80.2) 0.3 (0.21–0.48) * 0.2 (0.05–0.91)
Good 631 (58.3) 185 (29.3) 446 (70.7) 0.6 (0.39–0.81) * 0.4 (0.09–1.63)
Bad 11 (1.0) 6 (54.6) 5 (45.4) 1
Chronic illness
Yes 70 (6.5) 35 (50.0) 35 (50.0) 1.3 (0.79–2.09) 1.0 (0.54–1.68)
No 1012 (93.5) 243 (24.0) 769 (76.0) 1
Smoking status
Yes 90 (8.3) 26 (28.9) 64 (71.1) 0.5 (0.3–0.79) * 1.1 (0.55–2.14)
No 992 (91.7) 252 (25.4) 740 (74.6) 1
Alcohol use
Yes 147 (13.6) 48 (32.6) 99 (67.4) 0.6 (0.39–0.82) * 0.8 (0.53–1.27)
No 935 (86.4) 230 (24.6) 705 (75.4) 1
Pregravid body mass index (kg/m2)
Underweight (<18.5) 22 (2.0) 4 (18.2) 18 (81.8) 0.1 (0.05–0.35) * 0.2 (1.07–1.11)
Normal weight (18.5–24.9) 917 (84.8) 200 (21.8) 717 (78.2) 0.9 (0.62–1.14) 0.9 (0.69–1.34)
Overweight (25.0–29.9) 143 (13.2) 74 (51.7) 69 (48.3) 1
Planned pregnancy
Yes 351 (32.4) 101 (28.8) 250 (71.2) 1.9 (1.48–2.47) * 1.2 (0.81–1.64)
No 731 (67.6) 177 (24.2) 554 (75.8)
Physical activity advice
Yes 382 (35.3) 116 (30.4) 266 (69.6) 2.1 (1.66–2.76) * 1.3 (0.92–1.72)
No 700 (64.7) 162 (23.1) 538 (76.9) 1
Physical activity before pregnancy
Yes 378 (34.9) 123 (32.5) 255 (67.5) 2.7 (2.1–3.51) * 1.3 (0.77–2.05)
No 704 (65.1) 155 (22.0) 549 (78.0) 1
Physical activity gestational period
1st trimester 188 (17.4) 62 (33.0) 126 (67.0) 3.2 (2.34–4.47) * 1.9 (1.06–3.31) *
2nd trimester 114 (10.5) 45 (39.5) 69 (60.5) 3.0 (2.03–4.37) * 2.0 (1.10–3.70) *
3rd trimester 27 (10.5) 15 (55.6) 12 (44.4) 1.3 (0.79–2.07) 1.0 (0.38–2.57)
Never 753 (69.6) 156 (20.7) 597 (79.3) 1

COR = Crude Odds Ratio, AOR = Adjusted Odds Ratio, CI = Confidence Interval; * Statistically significant.

In order to determine the best fitting model, an automatic variable selection procedure was used. Automatic variable selection procedures are statistical tools for choosing the best subset of predictor variables for a given response variable. The estimated logistic regression model identified age, residential area, education, employment status, parity and timing of exercise as significant predictors of physical activity during pregnancy (Table 4 and Table 5). The effects of these variables on physical activity indicated that women <19 years (AOR = 0.3; CI: 0.16–0.76), from a semi-urban area (AOR = 0.8; CI: 0.55–1.03), with primary level education (AOR = 0.5; CI: 0.20–0.71), unemployed (AOR = 0.5; CI: 0.29–0.77) and nulliparous (AOR = 0.6; CI: 0.28–1.31) were significantly less likely to participate in physical activity during pregnancy compared to older women, those from urban and rural areas, with at least a secondary school education, employed and who were primiparous or multiparous, respectively. Conversely, women who started physical activity in their first trimester (AOR = 1.9; CI: 1.06–3.31) were significantly more likely to be physically active during pregnancy compared to women commencing physical activity in the second trimester. All other variables such as race, marital status, religion, family support, previous mode of delivery, antepartum haemorrhage, smoking and consuming alcohol during pregnancy, pregravid body mass index (kg/m2), physical activity advice and physical activity before pregnancy were not associated with physical activity during pregnancy.

4. Discussion

To our knowledge, this is the first study to determine the prevalence of leisure-time physical activity participation during pregnancy and associated factors among pregnant women in the Eastern Cape Province of South Africa. Exploring the socio-demographic, behavioural, maternal and clinical factors affecting prenatal physical activity in this setting, where no previous information exist, might help in formulating policies that are key to improving maternal prenatal healthcare to this special population. From a clinical and health standpoint, physical activity participation during pregnancy confers many benefits and should be promoted, encouraged and sustained during, and even beyond pregnancy to avoid sedentary—and obesity—associated risks [16]. The interplay of socio-demographic, behavioural, maternal and clinical factors affecting physical activity during pregnancy warrant contextual understanding of the dimensionality of the factors at play to detect possible deficits and inform context-specific interventions. Contextual knowledge of factors influencing prenatal activity is a key component of the provision of quality antenatal and obstetric healthcare services for pregnant women. The findings of this study show few (25.7%) women engage in moderate-intensity physical activity. Conversely, 74.3% women do not meet the international physical activity recommendation of 150 min per week during pregnancy. The factors driving prenatal physical activity varies from one geographic setting to another.

A comparison of the rates of physical activity participation during pregnancy in this study with rates of physical activity in South Africa indicates a lower physical activity rate of 17.0% in Gauteng [39], whilst in Western province it was reported 44% and 12% women participated in light physical activity and moderate physical activity, respectively [40]. In the Watson longitudinal study of pregnant women in Gauteng province, 50.6% women were inactive in the second trimester and their physical activity decreased as pregnancy progressed [17]. Expectedly, it is thought that pregnant women in Africa and other low-income settings would exhibit relatively high physical activity, presumably because of the traditional gender-household role prescription for women, where women are to perform virtually all the household activities; however, this seems not be the case in our results. Notably, the low prenatal activity observed among women in this current study resonates with the global physical inactivity reported among pregnant women in both developed and developing countries. In addition, low prenatal physical activity have been reported in Nigeria (13.6%, 10.2%) [18,46], Ethiopia (21.9%, 8.4%) [13,21], Norway (14.6%) [50], China (11.1%) [23], and Brazil (20.1%) [16]. The lesser participation of women in moderate-intensity physical activity during pregnancy in this present study reflects the pattern of prenatal physical activity reported in low-income countries. Some studies have shown that low resources and lack of social support affect the level of physical activity practice among pregnant women in South Africa [37,40]. Clearly, the majority of the women (67.7%) in our study were unemployed, however received social support, but engage less in moderate-intensity physical activities. The issues of non-availability of facilities, resources, and lack of knowledge on physical activity and advice from healthcare providers are possible reasons for this low participation in moderate-intensity physical activity during pregnancy among women in this study. About 64.7% of the women reported receiving no physical activity advice from the healthcare providers. In addition, the wave of industrialisation and modernisation taking place in South Africa, particularly in urban areas, could serve as facilitators of physical inactivity. This partly explains the results of our finding. Since the post-apartheid era, the lifestyle behaviour of most South Africans has changed dramatically as a result of the effects of modernisation and urbanisation which promote physical inactivity and associated health risks. Generally, there is low physical activity participation among the South African populations. The South Africa National Health and Nutrition Examination Survey reported that 46% of South Africans are physically inactive [51], and pregnant women are most at high risk of being inactive and sedentary [17].

From the clinical and public health perspective, there is a need to formulate policies and programmes regarding physical activity participation during pregnancy. In the South African context, a plausible strategy to promote women’s awareness and knowledge on prenatal physical activity during pregnancy, and further encourage them to increase leisure-time physical activity, and engage in moderate-intensity physical activities is to utilise and promote the Ward-Based Outreach Teams in the community or women’s groups to promote awareness regarding the health benefits of physical activity on maternal health. This is particularly very relevant and important because the Ward-Based Outreach Teams primary focus is to promote community health by providing door-to-door health screening services and to sensitise or create awareness on various health issues in the community and schools. Community beliefs could have considerable influence on physical activity during pregnancy; therefore, efforts to enhance leisure-time, and moderate-intensity physical activity during pregnancy should be intensified. Healthcare providers (nurses, midwives, gynaecologists, physicians) should encourage women to practice moderate physical activity during pregnancy, also reinforcing the contribution of maintaining daily activities to maternal health. Pregnancy is a phase in which women are willing to alter their lifestyle behaviour, if motivated to do so.

The finding of this study shows that household activities contributed most to the total activity performed by the women. The most activities performed were of light intensity, as only a few of the pregnant women participate in moderate-to-vigorous intensity physical activity. This finding mirrors an earlier nationally representative population-based survey of 26,339 individuals, in which less than half of South Africans were moderately or vigorously physically active [52]. Our finding is consistent with other previous studies in South Africa [17,39], which reported 76.9% and 80.0% prevalence rates of household chores and walking, respectively. Similarly, household and occupational activities were reported as the most preferred physical activity performed by women during pregnancy in China [53,54], Ethiopia [13,21], Taiwan [55], Nigeria [56], Portugal [57], Serbia [14], and Brazil [16]. Pregnant women often state that family and household obligations or fear of injuries prevent them from initiating and participating in physical activity [58]; as such, it is possible that most of the pregnant women will feel more comfortable and safer doing household activities than engaging in occupational or sporting activities during pregnancy [21]. This perhaps explains the reason for the highest amount of energy being expended on household, occupational and transportation activities among pregnant women currently. In a previous study of pregnant women in South Africa, women considered physical activity as an activity of daily living, such as occupational and household tasks. They, however, perceived certain occupational, household and recreational tasks as too vigorous and consequently unsafe; the safety or otherwise of vigorous activity during pregnancy was informed by advice from family and friends, or listening to their own bodies [37]. It might be possible that the women lack access, education and support for other physical activities, which explains why majority of the women are engaged in household activities. There is need for context-specific interventions to educate and encourage pregnant women to participate in moderate-intensity physical activity to achieve optimal maternal health outcomes.

The advocacy philosophy imbibed by the UK guidelines with a dictum ‘every activity counts’ emphasising the need for inactive pregnant women to make an effort to accumulate physical activity throughout the week [59], is something to learn from and apply in the South African context. In this regard, periodic workshops on prenatal physical activity, involving a multidisciplinary team (exercise physiologists, physiotherapists, gynaecologists, obstetricians) to provide talks on the importance of engaging in, and types of moderate-intensity activities for their health and the baby is advocated. Another possible intervention strategy is to involve other exercise specialists such as exercise physiologists, physiotherapists and biokineticists (who practice exclusively in South Africa) to provide prenatal physical activity programmes, and social support within the community. By way of definition, biokineticists are exercise therapists that prescribe individualised exercise and physical activity for rehabilitation and promotion of health and quality of life [60]. In addition, utilising mHealth technology—MomConnect to promote awareness on prenatal physical activity and to encourage women to participate actively in household physical activities during pregnancy is a feasible option in South African context. The ‘MomConnect’ is a phone-based technological maternal health programme by the South African National Department of Health to support and encourage women to maintain and live healthy lifestyles during and after pregnancy, as well promote child health. The ‘MomConnect’ health promotion messages are freely available to the user. Research on exploring contextually relevant interventions to encourage pregnant women to increase leisure-time physical activity and promote moderate-intensity activities during pregnancy in this setting is desirable.

In the estimated multivariate logistic regression model, women whose age was <19 years (AOR = 0.3; CI: 0.16–0.76) were less likely to be actively engage in moderate physical activity during pregnancy compared to women 19–34 years. Conversely, in Hailemariam et al. [13] study in Ethiopia it was reported that women who were 26–35 years were 2.69 times more likely to be sedentary (AOR: 2.69, 95% CI: 1.07–6.78) compared with those in the age category of 16–25 years. Similar studies have reported age as a predictor of prenatal active practice [21,61].

Strangely, the finding of this study show that women residing in a semi-urban area (AOR = 0.8; CI: 0.55–1.03) are significantly less likely to engage in moderate physical activity compared to those who are in urban and rural settings. A recent study in Poland indicated that more pregnant women in urban than in rural areas performed physical activity during pregnancy [62]. The place of residence may have a relative influence on the extent of physical activity during pregnancy, based on safety issues, information, and infrastructural opportunities. However, these variables are out of the scope of the paper. Research exploring the factors influencing physical activity and place of residence during pregnancy would provide an insight on how best to tailor interventions to address environmental and cultural variables operating at the spectrum of prenatal activity promotion.

In this study, women with a low level of education were less likely to engage in moderate physical activity during pregnancy compared to women with a secondary level of education. This finding is similar to studies conducted in Ethiopia [13,21], Brazil [16], Serbia [14], Netherlands [63], and Nigeria [46]. In contrast, other studies found positive associations between high educational and physical activity levels [64,65,66,67]. We recognised lower levels of education in the present study. The majority of the participants have completed secondary education or have less than secondary level education (74.2%). This suggests that women with higher educational levels are better informed or have more access to knowledge about physical activity during pregnancy [21,23]. Women with lower education should be well-informed with the benefits of physical activity, and prenatal healthcare programmes should focus on prenatal physical activity to encourage women to engage in moderate-intensity physical activity for better maternal and foetal health outcomes. Providing such information to women during antenatal visits might change their attitude to prenatal physical activity and motivate them to, at least, participate in household physical activities. Women should be provided with pamphlets and possibly DVD’s that contain information on prenatal physical activities, and posters displayed at the antenatal clinics, as these will help create awareness on prenatal physical activity. We postulate that non-formal prenatal physical activity advice that may be provided to the women at the antenatal clinics in South Africa may not be sufficient, lacking in content, because not all health providers possess adequate scientific knowledge on prenatal physical activity. Therefore, adopting a systematic or formalized clinic-based prenatal physical activity intervention guide is advocated and, in this context, the training of health providers on the types, intensity, duration and physical activity recommendations during pregnancy is important, in order to bridge their knowledge gap on the subject matter.

Our findings demonstrated that being unemployed was significantly associated with a lower likelihood of prenatal physical activity compared with those who are employed. Maternal employment influences physical activity participation during pregnancy. In this study, consistent with studies conducted in Ethiopia [13], Nigeria [46] and Netherlands [63], unemployed women were more likely to be physically active than employed women. It is plausible that unemployed women have enough time to stay at home, not having the economic power to hire a domestic helper; therefore, they themselves then perform most of the household/caring activities. This is not surprising because most of the women in this present study participate in light intensity and household activities. A combination of a lower education level and household income, in this case, unemployment, entails less chance of engagement in leisure-time physical activity because the women may be lacking the social and environmental resources and information as impetus to initiate and practice physical activity [68,69]. Therefore, addressing the social and environmental factors affecting their prenatal physical activity practice would help facilitate other efforts to encourage women to participate in prenatal physical activity of moderate-intensity to improve their health and that of the unborn baby.

Our study indicated that nulliparous women are significantly less likely to be physically active during pregnancy compared to those who are primiparous or multiparous, respectively. Similar to other studies, multiparous women exhibit more physical activeness than their nulliparous peers [13,70,71], whilst previous studies have found no statistically significant association between parity and physical activity during pregnancy [72,73]. In this regard, childcare interventions are necessary to encourage women to engage in physical activity together with their children to promote the uptake of moderate-intensity physical activity during pregnancy.

However, our finding demonstrated from the predictive model that pregnant women who commence physical activity in the first trimester are significantly more likely to be physically active during pregnancy compared to those who start later than the second trimester. This is concordant with a study in Poland [61], and USA [15] which found the odds of meeting physical activity recommendations, including both moderate and vigorous activities, to be higher among women in the first trimester compared to the third trimester. However, our finding is inconsistent with the findings from other previous studies, which indicated that women in the third trimester were more likely to meet the physical activity guideline compared to those in the first trimester [17,54,65,74,75]. Although the present study did not probe for the cessation of physical activity, notably, the decrease in physical activity in the second and the third trimesters of pregnancy can be attributed to women’s mood changes and the unborn baby’s foetal growth, which result in weight gain and discomforts such as fatigue, back pain, and sleeplessness [76,77]. Women should be encouraged to engage and sustain their prenatal activity throughout pregnancy, and beyond. This is particularly important and relevant to women with no pregnancy complications and contraindications; pregnant women, therefore, should be advised to undertake moderate-intensity physical activity, accumulating at least 150 min per week, as stipulated by international bodies.

5. Implications

Our findings have emphasised the need to tailor health promotion interventions in the promotion of moderate-intensity physical activity in the antenatal healthcare as part of the primary healthcare agenda. Healthcare providers should regard physical activity as a prescription, rather than an option to be observed. The findings highlight several factors associated with low level of prenatal physical activity among pregnant women in this setting, which call for a context-specific and multidisciplinary approach to the promotion of prenatal activity, particularly focusing on household and moderate-intensity activities. Understandably, the demographic correlates of prenatal physical activity provide useful information on the variables affecting prenatal physical activity; such information is relevant to inform interventions and to identify those who need intervention. For example, as in this case, interventions focusing on women with a low level of education and without employment are imperative. Stakeholders, such as the Eastern Cape Department of Health, research organizations, local NGOs working with pregnant women, and faith-based organisations or societies should provide relevant and appropriate strategies that include educational interventions to address barriers to moderate physical activity during pregnancy. Notably, programs or pamphlets, posters showing information and instructions on physical activity during pregnancy are absent in the routine of the pregnant population in South Africa. As such, it is desirable that health policy makers, health providers, and stakeholders working with pregnant population prioritise physical activity for all pregnant women.

6. Limitations

One obvious limitation of the study is the use of a self-reported questionnaire, which could have inherent bias in the manner of responses, and the PPAQ questionnaire was not validated locally against objective methods; as such, we cannot draw conclusion on its measurement properties (reliability, criterion validity, construct validity, responsiveness) in the South African context. Therefore, future studies on the validity of the PPAQ in this population are warranted, and studies using objective measure, such as an accelerometer to evaluate physical activity during pregnancy. Furthermore, the PPAQ is reported to have insufficient construct validity in assessing total and vigorous physical activity scores in pregnancy, however, with low-to-moderate quality evidence [78]. In addition, the participants were pregnant women attending public health facilities in Buffalo City Municipality of the Eastern Cape; as such, this limited the generalisability of the findings to the entire Eastern Cape Province. Despite these limitations, our study provides useful information for future comparative studies on the factors, types and intensity of physical activity participation during pregnancy in the Eastern Cape Province of South Africa. We believe such information would be relevant in shaping maternal health interventions in the context of promotion of leisure-time physical activity, at least in this setting. Again, the prospective evaluation of physical activity using the PPAQ, a simple and short, reliable and valid tool, which has been used in several countries [47,79,80,81,82,83,84], and the large sample of pregnant women serve as unique strengths of the study. To the best of the author’s knowledge, previous studies examining physical activity during pregnancy in South Africa have not utilised such a large population as ours. In addition, contrary to other previous published studies, our study involved all racial groups in the South African context with varying sociodemographic characteristics.

7. Conclusions

The findings of this study demonstrated low participation of women in moderate-intensity physical activity during pregnancy. The majority of the women did not meet the 150 min per week recommendations. Light intensity and household activities were the predominant forms of physical activity among pregnant women. The factors affecting physical activity of women in this present study included age, residential area, lower educational level, unemployment, nulliparity and trimester timing of exercise as significant predictors of physical activity during pregnancy. There exists a need to provide basic education to mothers, and a general advocacy campaign on the health benefits of moderate-intensity physical activity during pregnancy for optimal participation in prenatal activity should also be launched.

Acknowledgments

This work is based on the research supported wholly by the National Research Foundation of South Africa. We thank the participants for participating in the study; the Eastern Cape Department of Heath for granting permission to conduct the study in selected health facilities in Buffalo City Metro Municipality District; and the Research Assistants for their assistance in data collection.

Author Contributions

Conceptualization and drafting of manuscript, U.B.O. and D.T.G. Data collection, U.B.O. Review and editing, D.T.G. Supervision, D.T.G. All authors have read and agreed to the published version of the manuscript.

Funding

UBO received a Doctoral Research Grant from National Research Foundation of South Africa.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.American College of Obstetricians and Gynaecologists Physical Activity and Exercise During Pregnancy and the Postpartum Period: ACOG Committee Opinion, Number 804. Obstet. Gynaecol. 2020;135:e178–e188. doi: 10.1097/AOG.0000000000003772. [DOI] [PubMed] [Google Scholar]
  • 2.U.S. Department of Health and Human Services . Physical Activity Guidelines for Americans. U.S. Department of Health and Human Services; Washington, DC, USA: 2018. [Google Scholar]
  • 3.World Health Organization WHO Homepage. [(accessed on 16 December 2019)]; Available online: www.who.int.
  • 4.Mottola M.F., Davenport M.H., Ruchat S.M., Davies G.A., Poitras V., Gray C., Jaramillo Garcia A., Barrowman N., Adamo K.B., Duggan M., et al. No. 367-2019 Canadian Guideline for Physical Activity throughout Pregnancy. J. Obstet Gynaecol Can. 2018;40:1528–1537. doi: 10.1016/j.jogc.2018.07.001. [DOI] [PubMed] [Google Scholar]
  • 5.The Royal Australian New Zealand College of Obstetricians and Gynaecologists (RANZCOG) Exercise during Pregnancy. [(accessed on 17 October 2020)];2016 Available online: https://ranzcog.edu.au/womens-health/patient-information-resources/exercise-during-pregnancy.
  • 6.Bø K., Artal R., Barakat R., Brown W.J., Davies G.A.L., Dooley M., Evenson K.R., Haakstad L.A.H., Kayser B., Kinnunen T.I., et al. Exercise and pregnancy in recreational and elite athletes: 2016/2017 evidence summary from the IOC expert group meeting, Lausanne. Part 5. Recommendations for health professionals and active women. Br. J. Sports Med. 2018;52:1080–1085. doi: 10.1136/bjsports-2018-099351. [DOI] [PubMed] [Google Scholar]
  • 7.Department of Health & Social Care UK Chief Medical Officer’s physical activity guidelines. [(accessed on 17 October 2020)];2019 Available online: https://assestts.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/832868/ukchief-medical-officersphysical-activity-guidelines.pdf.
  • 8.Sports Medicine Australia Sports Medicine Australia statement: The benefits and risks of exercise during pregnancy. J. Sci. Med. Sport. 2002;5:11–19. doi: 10.1016/S1440-2440(02)80293-6. [DOI] [PubMed] [Google Scholar]
  • 9.Pescatello L.S., Arena R., Riebe D., Thompson P.D. ACSM’s Guidelines for Exercise Testing and Prescription. 9th ed. American College of Sports Medicine; Baltimore, MD, USA: 2014. [DOI] [PubMed] [Google Scholar]
  • 10.Di Fabio D.R., Blomme C.K., Smith K.M., Welk G.J., Campbell C.G. Adherence to physical activity guidelines in mid-pregnancy does not reduce sedentary time: An observational study. Int. J. Behav. Nutr. Phys. Act. 2015;12:27. doi: 10.1186/s12966-015-0191-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Bauer C., Graf C., Platschek A.M., Struder H.K., Ferrari N. Reasons, motivational factors, and perceived personal barriers to engagement in physical activity during pregnancy vary within the BMI classes: The Prenatal Prevention Project Germany. J. Phys. Act. Health. 2018;15:204–211. doi: 10.1123/jpah.2016-0563. [DOI] [PubMed] [Google Scholar]
  • 12.Schmidt T., Heilmann T., Savelsberg L., Maass N., Weisser B., Eckmann-Scholz C. Physical exercise during pregnancy—How active are pregnant women in Germany and how well informed? Geburtshilfe Frauenheilkd. 2017;77:508–515. doi: 10.1055/s-0043-107785. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Hailemariam T.T., Gebregiorgis Y.S., Gebremeskel B.F., Haile T.G., Spitznagle T.M. Physical activity and associated factors among pregnant women in Ethiopia: Facility-based cross-sectional study. BMC Preg. Childbirth. 2020;20:92. doi: 10.1186/s12884-020-2777-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Todorovic J., Terzic-Supic Z., Bjegovic-Mikanovic V., Piperac P., Dugalic S., Gojnic-Dugalic M. Factors associated with the leisure-time physical activity (LTPA) during the first trimester of the pregnancy: The cross-sectional study among pregnant women in Serbia. Int. J. Environ. Res. Public Health. 2020;17:1366. doi: 10.3390/ijerph17041366. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Padmapriya N., Shen L., Soh S.E., Shen Z., Kwek K., Godfrey K.M., Gluckman P.D., Chong Y.S., Saw S.M., Müller-Riemenschneide F. Physical activity and sedentary behaviour patterns before and during pregnancy in a multi-ethnic sample of Asian women in Singapore. Matern. Child. Health J. 2015;19:2523–2535. doi: 10.1007/s10995-015-1773-3. [DOI] [PubMed] [Google Scholar]
  • 16.Nascimento S.L., Surita F.G., Godoy A.C., Kasawara K.T., Morais S.S. Physical activity patterns and factors related to exercise during pregnancy: A cross sectional study. PLoS ONE. 2015;10:e0128953. doi: 10.1371/journal.pone.0128953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Watson E.D., Van Poppel M.N.M., Jones R.A., Norris S.A., Micklesfield L.K. Are South African mothers moving? Patterns and correlates of physical activity and sedentary behaviour in pregnant black South African women. J. Phys. Act. Health. 2017;14:329–335. doi: 10.1123/jpah.2016-0388. [DOI] [PubMed] [Google Scholar]
  • 18.Lawan A., Awotidebe A.W., Oyeyemi A.L., Rufa A.A., Oyeyemi A.Y. Relationship between physical activity and health related quality of life among pregnant women. Afr. J. Reprod. Health. 2018;22:80–89. doi: 10.29063/ajrh2018/v22i3.9. [DOI] [PubMed] [Google Scholar]
  • 19.Zhang J., Savitz D.A. Exercise during pregnancy among US women. Ann. Epidemiol. 1996;6:53–59. doi: 10.1016/1047-2797(95)00093-3. [DOI] [PubMed] [Google Scholar]
  • 20.Domingues M., Santos I., Matijasevich A., Horta B.L., Hallal P.C., Coll C. Changes in Leisure-Time Physical Activity from the Prepregnancy to the Postpartum Period: 2004 Pelotas (Brazil) Birth Cohort Study. J. Phys. Act. Health. 2016;13:361–365. doi: 10.1123/jpah.2015-0324. [DOI] [PubMed] [Google Scholar]
  • 21.Gebregziabher D., Berhe H., Kassa M., Berhanie E. Level of physical activity and associated factors during pregnancy among women who gave birth in Public Zonal Hospitals of Tigray. BMC Res. Notes. 2019;12:454. doi: 10.1186/s13104-019-4496-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Put W.M., Chuang S., Chan L., Lin-Wai C. Physical activity in pregnancy: Attitudes and practices of Hong Kong Chinese women. Hong Kong J. Gynaecol. Obstet. Midwifery. 2015;15:38–147. [Google Scholar]
  • 23.Zhang Y., Dong S., Zuo J., Hu X., Zhang H., Zhao Y. Physical activity level of urban pregnant women in Tianjin, China: A cross-sectional study. PLoS ONE. 2014;9:e109624. doi: 10.1371/journal.pone.0109624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Bacchi E., Bonin C., Zanolin M.E., Zambotti F., Livornese D., Donic S., Bonora E., Baldisser G., Ihnatava T., Di Sarra D., et al. Physical activity patterns in normal-weight and overweight/obese pregnant women. PLoS ONE. 2016;11:e0166254. doi: 10.1371/journal.pone.0166254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Coll C.V., Domingues M.R., Gonçalves H., Bertoldi A.D. Perceived barriers to leisure-time physical activity during pregnancy: A literature review of quantitative and qualitative evidence. J. Sci. Med. Sport. 2017;20:17–25. doi: 10.1016/j.jsams.2016.06.007. [DOI] [PubMed] [Google Scholar]
  • 26.Davenport M.H., Ruchat S.M., Poitras V.J., Jaramillo Garcia A., Gray C.E., Barrowman N., Skow R.J., Meah V.L., Riske L., Sobierajski F., et al. Prenatal exercise for the prevention of gestational diabetes mellitus and hypertensive disorders of pregnancy: A systematic review and meta-analysis. Br. J. Sports Med. 2018;52:1367–1375. doi: 10.1136/bjsports-2018-099355. [DOI] [PubMed] [Google Scholar]
  • 27.Davenport M.H., Ruchat S.M., Sobierajski F., Poitras V.J., Gray C.E., Yoo C., Skow R.J., Jaramillo Garcia A., Barrowman N., Meah V.L., et al. Impact of prenatal exercise on maternal harms, labour and delivery outcomes: A systematic review and meta-analysis. Br. J. Sports Med. 2019;53:99–107. doi: 10.1136/bjsports-2018-099821. [DOI] [PubMed] [Google Scholar]
  • 28.Davenport M.H., Kathol A.J., Mottola M.F., Skow R.J., Meah V.L., Poitras V.J., Jaramillo Garcia A., Gray C.E., Barrowman N., Riske L., et al. Prenatal exercise is not associated with fetal mortality: A systematic review and meta-analysis. Br. J. Sports Med. 2019;53:108–115. doi: 10.1136/bjsports-2018-099773. [DOI] [PubMed] [Google Scholar]
  • 29.Micklesfield L.K., Pedro T.M., Kahn K., Kinsman J., Pettifor J.M., Tollman S., Norris S.A. Physical activity and sedentary behaviour among adolescents in rural South Africa: Levels, patterns and correlates. BMC Public Health. 2014;14:40. doi: 10.1186/1471-2458-14-40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Van Biljon A., McKune A.J., DuBose K.D., Kolanisi U., Semple S.J. Physical activity levels in urban-based South African learners: A cross-sectional study of 7348 participants. South. Afr. Med. J. 2018;108:126–131. doi: 10.7196/SAMJ.2018.v108i2.12766. [DOI] [PubMed] [Google Scholar]
  • 31.Seme Z., de Villiers A., Steyn N.P., Senekal M. Food choices, physical activity levels and other factors associated with weight gain in primary school educators. J. Con. Sci. 2017;2 doi: 10.4314/jfecs.v0i0. [DOI] [Google Scholar]
  • 32.Tomaz S.A., Jones R.A., Hinkley T., Twine R., Kahn K., Norris S.A., Draper C.E. Physical activity in early childhood education and care settings in a low-income, rural South African community: An observational study. Rural Remote Health. 2019;19:5249. doi: 10.22605/RRH5249. [DOI] [PubMed] [Google Scholar]
  • 33.Oyeyemi A.L., Moss S.J., Monyeki M.A., Kruge H.S. Measurement of physical activity in urban and rural South African adults: A comparison of two self-report methods. BMC Public Health. 2016;16:1004. doi: 10.1186/s12889-016-3693-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Kunene S.H., Taukobong N.P. Level of physical activity of health professionals in a district hospital in KwaZulu-Natal, South Africa. South. Afr. J. Physiother. 2015;71:234. doi: 10.4102/sajp.v71i1.234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Skaal L. Factors influencing health workers’ participation in physical activity in one public hospital in South Africa: Do health workers have barriers to exercise? Afr. J. Phy. Health Edu. Recreat. Dance. 2011;17:813–823. [Google Scholar]
  • 36.Dickie K., Micklesfield L.K., Chantler S., Lambert E.V., Goedecke J.H. Cardiorespiratory fitness and light-intensity physical activity are independently associated with reduced cardiovascular diseases risk in urban black South Africa women: A cross-sectional study. Metabol. Syndr. Relat. Disord. 2016;14:23–32. doi: 10.1089/met.2015.0064. [DOI] [PubMed] [Google Scholar]
  • 37.Watson E.D., Norris S.A., Draper C.E., Jones R.A., van Poppel M.N.M., Micklesfield L.K. “Just because you’re pregnant, doesn’t mean you’re sick!” A qualitative study of beliefs regarding physical activity in black South African women. BMC Preg. Childbirth. 2016;16:174. doi: 10.1186/s12884-016-0963-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Watson E.D., Brage S., White T., Westgate K., Norris S.A., Van Poppel M.N.M., Micklesfield L.K. The influence of objectively measured physical activity during pregnancy on maternal and birth outcomes in urban black South African women. Matern. Child. Health J. 2018;22:1190–1199. doi: 10.1007/s10995-018-2504-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Brunette E.L., Kotze J., Wood P.S., Du Toit P.J., Grant C.C. An epidemiological study of physical activity patterns and weight gain in physically active and sedentary pregnant women in Tshwane, South Africa. Afr. J. Phy. Health Edu. Recreat. Dance. 2012;18(Suppl. S1):132–143. [Google Scholar]
  • 40.Muzigaba M., Kolbe-Alexander T.L., Wong F. The perceived role and influencers of physical activity among pregnant women from low socioeconomic status communities in South Africa. J. Phys. Act. Health. 2014;11:1276–1283. doi: 10.1123/jpah.2012-0386. [DOI] [PubMed] [Google Scholar]
  • 41.Okafor U.B., Goon D.T. Developing a physical activity intervention strategy for pregnant women in Buffalo City Municipality, South Africa: A study protocol. Int. J. Environ. Res. Public Health. 2020;17:6694. doi: 10.3390/ijerph17186694. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Eastern Cape Socio Economic Consultative Council Buffalo City Metro Municipality Socio Economic Review and Outlook. [(accessed on 14 September 2020)];2020 Available online: https://www.ecsecc.org/documentrepository/informationcentre/buffalo-city-metro-municipality_44557.pdf.
  • 43.Sarmah H.K., Hazarika B.B., Choudhury G. An investigation on effect of bais on determination of sample size on the basis of data related to the students of schools of Guwahati. Int. J. Appl. Math. Stat. Sci. 2013;2:33–48. [Google Scholar]
  • 44.Mottola M.F., Davenport M.H., Ruchat S., Davies G.A., Poitras V.J., Gray C.E., Jaramillo Garcia A., Barrowman N., Adamo K.B., Duggan M., et al. 2019 Canadian guideline for physical activity throughout pregnancy. Br. J. Sport Med. 2018;40:1339–1346. doi: 10.1136/bjsports-2018-100056. [DOI] [PubMed] [Google Scholar]
  • 45.Chasan-Taber L., Schmidt M.D., Roberts D.E., Hosmer D., Markenson G., Freedson P.S. Development and validation of a Pregnancy Physical Activity Questionnaire. Med. Sci. Sports Exerc. 2004;36:1750–1760. doi: 10.1249/01.MSS.0000142303.49306.0D. [DOI] [PubMed] [Google Scholar]
  • 46.Adeniyi A.F., Ogwumike O.O., Osinike C.I. Physical activity and energy expenditure: Findings from the Ibadan pregnant women’s survey. Afr. J. Reprod. Health. 2014;18:117–126. [PubMed] [Google Scholar]
  • 47.Chandonnet N., Saey D., Almeras N., Marc I. French Pregnancy Physical Activity Questionnaire compared with an accelerometer cut point to classify physical activity among pregnant obese women. PLoS ONE. 2012;7:e38818. doi: 10.1371/journal.pone.0038818. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Institute of Medicine and National Research Council . Weight Gain during Pregnancy: Reexamining the Guidelines. The National Academies Press; Washington, DC, USA: 2009. [PubMed] [Google Scholar]
  • 49.Centers for Disease Control and Prevention Healthy Pregnant or Postpartum Women. [(accessed on 10 September 2020)];2015 Available online: https://www.cdc.gov/physicalactivity/basics/pregnancy/index.htm.
  • 50.Gjestland K., Bo K., Owe K.M., Eberhard-Gran M. Do pregnant women follow exercise guidelines? Prevalence data among 3482 women, and prediction of low-back pain, pelvic girdle pain and depression. Br. J. Sports Med. 2012;47:515–520. doi: 10.1136/bjsports-2012-091344. [DOI] [PubMed] [Google Scholar]
  • 51.Shisana O., Labadarios D., Rehle T., Simbayi L., Zuma K., Dhansay A., Reddy P., Parker W., Hoosain E., Naidoo P., et al. South African National Health and Nutrition Examination Survey (SANHANES-1) HSRC Press; Cape Town, South Africa: 2013. [Google Scholar]
  • 52.Mlangeni L., Makola L., Naidoo I., Chibi B., Sokhela Z., Silimfe Z.M., Mabaso M. Factors associated with physical activity in South Africa: Evidence from a National Population Based Survey. Open J. Public Health. 2018;11:516–525. doi: 10.2174/1874944501811010516. [DOI] [Google Scholar]
  • 53.Yin Y., Huang Y., Liu X., Luo B. Assessment of physical activity status among pregnant women in southwestern China. Front. Nurs. 2019;6:135–141. doi: 10.2478/FON-2019-0020. [DOI] [Google Scholar]
  • 54.Xiang M., Zhang J., Liang H., Zhang Z., Konishi M., Hu H., Nishimak M., Kim H., Tabata H., Shimizu H., et al. Physical activity and dietary intake among Chinese pregnant women: An observational study. BMC Preg. Childbirth. 2019;19:295. doi: 10.1186/s12884-019-2452-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Lee C.F., Chiang I.C., Lin S.S., Lin H.M., Hsu C.J. Physical activity pattern and related factors among women during pregnancy. Formos. J. Med. 2012;16:103–111. [Google Scholar]
  • 56.Mbada C.E., Adebayo O.E., Adeyemi A.B., Arije O.O., Dada O.O., Akinwande O.A., Awotidebe T.O., Alonge I.B. Knowledge and attitude of Nigerian pregnant women towards antenatal exercise: A cross sectional survey. Obstet. Gynecol. 2014;1:8. doi: 10.1155/2014/260539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Santos P.C., Abreu S., Moreira C., Santos R., Ferreira M., Alves O., Moreira P., Mota J. Physical activity patterns during pregnancy in a sample of Portuguese women: A longitudinal prospective study. Iran. Red Crescent Med. J. 2016;18:e22455. doi: 10.5812/ircmj.22455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Marshall E.S., Bland H., Melton B. Perceived barriers to physical activity among pregnant women living in a rural community. Public Health Nurs. 2012;30:361–369. doi: 10.1111/phn.12006. [DOI] [PubMed] [Google Scholar]
  • 59.Smith R., Reid H., Matthews A., Calderwood C., Knight M., Foster C. Infographic: Physical activity for pregnant women. Br. J. Sports Med. 2018;52:532–533. doi: 10.1136/bjsports-2017-098037. [DOI] [PubMed] [Google Scholar]
  • 60.Ellapen T.J., Strydom G.L., Swanwpoel H.H.M., Hammill H., Paul Y. Biokineticist’s: A South African Health Profession evolving from Physical Education and Sport. In: Merc M., editor. Sport and Exercise Science. InTech Open; London, UK: 2018. [(accessed on 16 July 2020)]. Available online: https://www.intechopen.com/books/sport-and-exercise-science. [Google Scholar]
  • 61.Antosiak-Cyrak K.Z., Demuth A. A study of physical activity levels of pregnant women using the Polish version of Pregnancy Physical Activity Questionnaire (PPAQ-Pl) Ginekol. Pol. 2019;90:250–255. doi: 10.5603/GP.2019.0047. [DOI] [PubMed] [Google Scholar]
  • 62.Szubert M., Ilowiecka M., Wilczynski J., Bilinski P., Wojtyla C. Health-related behaviors of pregnant women residing in urban and rural areas in Poland. Int. J. Environ. Res. Public Health. 2020;17:4395. doi: 10.3390/ijerph17124395. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Merkx A., Ausems M., de Vries R., Nieuwenhuijze M.J. Factors affecting perceived change in physical activity in pregnancy. Midwifery. 2017;51:16–23. doi: 10.1016/j.midw.2017.05.007. [DOI] [PubMed] [Google Scholar]
  • 64.Sytsma T.T., Zimmerman K.P., Manning J.B., Jenkins S.M., Nelson N.C., Clark M.M., Boldt K., Borowski K.S. Perceived Barriers to Exercise in the First Trimester of Pregnancy. J. Perinat. Educ. 2018;27:198–206. doi: 10.1891/1058-1243.27.4.198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Da Silva S.G., Ricardo L.I., Evenson K.R., Hallal P.C. Leisure time physical activity in pregnancy and maternal-child health: A systematic review and meta-analysis of randomized controlled trials and cohort studies. Sports Med. 2017;47:295–317. doi: 10.1007/s40279-016-0565-2. [DOI] [PubMed] [Google Scholar]
  • 66.Mendinueta A., Esnal H., Arrieta H., Arrue M., Urbieta N., Ubillos I., Whitworth K.W., Delclòs-Alió X., Vich G., Ibarluzea J. What accounts for physical activity during pregnancy? A study on the sociodemographic predictors of self-reported and objectively assessed physical activity during the 1st and 2nd trimesters of pregnancy. Int. J. Environ. Res. Public Health. 2020;17:2517. doi: 10.3390/ijerph17072517. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Lindqvist M., Lindqvist M., Eurenius E., Persson M., Ivarsson A., Mogren I. Leisure time physical activity among pregnant women and its associations with maternal characteristics and pregnancy outcomes. Sex. Reprod. Healthc. J. 2016;9:14–20. doi: 10.1016/j.srhc.2016.03.006. [DOI] [PubMed] [Google Scholar]
  • 68.Sales-da-costa R., Werneck G.L., Lopes C.S., Faerstein E. Associação entre fatores sócio-demográficos e prática de atividade física de lazer no Estudo Pró-Saúde. Cad. Saude Publica. 2003;19:1095–1105. doi: 10.1590/S0102-311X2003000400031. [DOI] [PubMed] [Google Scholar]
  • 69.Cerin E., Leslie E. How socio-economic status contributes to participation in leisure-time physical activity. Soc. Sci Med. 2008;66:2596–2609. doi: 10.1016/j.socscimed.2008.02.012. [DOI] [PubMed] [Google Scholar]
  • 70.Lee C.F., Hwang F.M., Lin H.M., Chi L.K., Chien L.Y. The physical activity patterns of pregnant Taiwanese Women. J. Nurs. Res. 2016;24:291–299. doi: 10.1097/JNR.0000000000000158. [DOI] [PubMed] [Google Scholar]
  • 71.Lynch K.E., Landsbaugh J.R., Whitcomb B.W., Pekow P., Markenson G., Chasan-Taber L. Physical activity of pregnant Hispanic women. Am. J. Prev. Med. 2012;43:434–439. doi: 10.1016/j.amepre.2012.06.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Evenson K.R., Savitz D.A., Huston S.L. Leisure-time physical activity among pregnant women in the US. Paediatr. Perinat. Epidemiol. 2004;18:400–407. doi: 10.1111/j.1365-3016.2004.00595.x. [DOI] [PubMed] [Google Scholar]
  • 73.Chasan-Taber L., Schmidt M.D., Pekow P., Sternfeld B., Manson J.A., Markenson G. Correlates of physical activity in pregnancy among Latina women. Matern. Child. Health J. 2007;11:353–363. doi: 10.1007/s10995-007-0201-8. [DOI] [PubMed] [Google Scholar]
  • 74.De Haas S., Ghossein-Doha C., Van Kuijk S.M.J., Van Drongelen J., Spaanderman M.E.A. Physiological adaptation of maternal plasma volume during pregnancy: A systematic review and meta-analysis. Ultrasound Obstet. Gynecol. 2017;49:177–187. doi: 10.1002/uog.17360. [DOI] [PubMed] [Google Scholar]
  • 75.De Vargas Nunes Coll C., Domingues M.R., Hallal P.C., da Silva I.C.M., Bassani D.G., Matijasevich A., Barros A., Santos I.S., Bertoldi A.D. Changes in leisure-time physical activity among Brazilian pregnant women: Comparison between two birth cohort studies (2004–2015) BMC Public Health. 2017;17:119. doi: 10.1186/s12889-017-4036-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Evenson K.R., Moos M.K., Carrier K., Siega-Riz A.M. Perceived barriers to physical activity among pregnant women. Matern. Child. Health J. 2009;13:364–375. doi: 10.1007/s10995-008-0359-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Cramp A.G., Bray S.R. A prospective examination of exercise and barrier self-efficacy to engage in leisure-time physical activity during pregnancy. Ann. Behav. Med. 2009;37:325–334. doi: 10.1007/s12160-009-9102-y. [DOI] [PubMed] [Google Scholar]
  • 78.Sattler M.C., Jaunig J., Watson E.D., Van Poppel M.N.M., Mokkink L.B., Terwee C.B., Dietz P. Physical Activity Questionnaire for Pregnancy: A Systematic Review of Measurement Properties. Sports Med. 2018;48:2317–2346. doi: 10.1007/s40279-018-0961-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Adanaş A.G., Taşan H.A., Tarhan N., Çakar E., Şenol G.N., Ankaralı H., Tandoğan B. Reliability and validity of Turkish version of pregnancy physical activity questionnaire (PPAQ) in patients with gestational diabetes mellitus. J. Obstet. Gynaecol. 2020;40:176–181. doi: 10.1080/01443615.2019.1606178. [DOI] [PubMed] [Google Scholar]
  • 80.Çırak Y., Yılmaz G.D., Demir Y.P., Dalkılınç M., Yaman S. Pregnancy physical activity questionnaire (PPAQ): Reliability and validity of Turkish version. J. Phys. Ther. Sci. 2015;27:3703–3709. doi: 10.1589/jpts.27.3703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Krzepota J., Sadowska D., Sempolska K., Pelczar M. Measuring physical activity during pregnancy—Cultural adaptation of the Pregnancy Physical Activity Questionnaire (PPAQ) and assessment of its reliability in Polish conditions. Ann. Agric. Environ. Med. 2017;23:640–643. doi: 10.5604/12321966.1228390. [DOI] [PubMed] [Google Scholar]
  • 82.Suliga E., Sobaś K., Król G. Validation of the Pregnancy Physical Activity Questionnaire (PPAQ) Med. Stud. Stud. Med. 2017;33:40–45. doi: 10.5114/ms.2017.66955. [DOI] [Google Scholar]
  • 83.Xiang M., Konishi M., Hu H., Takahashi M., Fan W., Nishimaki M., Ando K., Kim H.K., Tabata H., Arao T., et al. Reliability and Validity of a Chinese-Translated Version of a Pregnancy Physical Activity Questionnaire. Matern. Child. Health J. 2016;20:1940–1947. doi: 10.1007/s10995-016-2008-y. [DOI] [PubMed] [Google Scholar]
  • 84.Han J.-W., Kang J.-S., Lee H. Validity and Reliability of the Korean Version of the Pregnancy Physical Activity Questionnaire. Int. J. Environ. Res. Public Health. 2020;17:5873. doi: 10.3390/ijerph17165873. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from International Journal of Environmental Research and Public Health are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES