Abstract
Background
Changes in movement behaviors – physical activity (PA), sedentary behavior, and sleep patterns – across preconception, pregnancy, and postpartum are associated with maternal and child health but remain understudied. Longitudinal accelerometer-measured data, including weekday-weekend differences, are lacking. Understanding these patterns is essential for developing targeted interventions that account for lifestyle variations. We investigated longitudinal changes in PA, sedentary behavior, and sleep patterns throughout preconception, pregnancy, and postpartum using prospectively collected accelerometry data.
Methods
In a Singapore prospective preconception cohort, women aged 18–45 wore an accelerometer on their non-dominant wrist for seven days during preconception (within one year of planned conception), mid-pregnancy (24–28 weeks), and 12-month postpartum. Valid data required measurements at all three or at least two consecutive timepoints (preconception-pregnancy or pregnancy-postpartum). Changes in PA (vigorous-, moderate-, and light-intensity), sedentary behavior, and sleep were analyzed using generalized estimating equations.
Results
Among 139 women (mean age: 30.8 years), most were under/normal weight (61.9%), Chinese (83.5%), had undergraduate education (59.0%), were employed (88.5%), and nulliparous (65.5%). Moderate- and vigorous-intensity PA decreased from preconception to mid-pregnancy, with vigorous-intensity PA remaining low postpartum, while moderate-intensity PA rebounded (daily mean [95% confidence interval] vigorous: 4.1 [2.8–5.4)], 1.7 [0–4.2], and 1.8 [0–5.0] min/day; moderate: 88.2 [82.8–93.5], 68.7 [58.6–78.7], and 90.2 [77.7–102.7] min/day, respectively). Light-intensity PA remained consistent from preconception to mid-pregnancy but increased postpartum (301.5 [289.6–313.5], 298.3 [273.1–323.5], and 340.1 [305.9–374.5] min/day, respectively). Sedentary behavior rose mid-pregnancy but decreased postpartum (618.2 [603.4–633.1], 639.6 [607.6–671.5], and 597.1 [553.5–640.7] min/day, respectively). Sleep duration remained stable from preconception to mid-pregnancy until postpartum, when it decreased (428.9 [420.6–437.3], 432.2 [412.2–452.1], and 408.4 [387.2–429.6] min/day, respectively). Moderate-/vigorous-intensity PA showed no weekday/weekend differences (daily percentage range, moderate: 4.7–6.6%; vigorous: 0.1–0.3%). Women engaged in less light-intensity PA on weekdays during mid-pregnancy and postpartum (weekdays: 20.5–23.2% versus weekends: 21.3–24.8%). Weekends showed lower sedentary behavior (weekdays: 42.5–45.4% versus weekends: 38.5–42.1%) and longer sleep duration (weekdays: 27.8–29.3% versus weekends: 29.8–32.0%) across all timepoints.
Conclusions
Sustained moderate- and vigorous-intensity PA from preconception through postpartum should be promoted, particularly vigorous-intensity PA recovery postpartum. Light-intensity PA, which increased postpartum, could be leveraged to reduce sedentary behavior, especially on weekdays. Given postpartum sleep decline, strategies to support maternal sleep, particularly on weekdays, are needed.
Clinical trial information
ClinicalTrials.gov, NCT03531658 (registered May 22, 2018).
Supplementary Information
The online version contains supplementary material available at 10.1186/s12889-025-26034-4.
Keywords: Preconception care, Pregnancy, Postpartum period, Accelerometry, Physical activity, Sedentary behaviors, Sleep, Movement, Cohort studies, Behavioral monitoring, Maternal health, Activity measurement, Longitudinal studies
Introduction
As key components of 24-h movement behaviors, physical activity, sedentary behavior, and sleep play crucial roles in maintaining lifelong well-being [1, 2]. Each behavior is unique, inherently displaces time available for others, emphasizing the constrained and reciprocal nature of daily movement patterns. Pregnancy and postpartum phases represent important stages of transition in a woman’s life, characterized by substantial physiological and lifestyle changes [3, 4], which may influence how women allocate time across these behaviors. Despite the well-documented health benefits of physical activity, global inactivity rates remain high, particularly among women [5]. Regular physical activity is associated with improved health outcomes across the reproductive lifespan, including preconception (e.g., infertility, polycystic ovary syndrome, weight management), pregnancy (e.g., reduced risk gestational diabetes, preeclampsia), and postpartum (e.g., weight retention, mental health) [6–8]. Similarly, sedentary behavior and sleep during pregnancy are integral to maternal health, with prolonged sedentary time linked to excessive gestational weight gain and diabetes [9, 10], and poor sleep associated with adverse maternal and child health [11].
Most existing research relied on self-reported data across various life stages: preconception-pregnancy [10, 12–15], pregnancy-postpartum [16–21], preconception-postpartum [15, 22–24], offering contextual insights but lacking the granularity of accelerometer-measured data. No accelerometry studies have comprehensively examined temporal trends in physical activity, sedentary behavior, and sleep throughout the entire preconception-to-postpartum transition. A previous cohort study [23], although prospective, relied on self-reported data and found increased walking but decreased moderate-to-vigorous physical activity (MVPA) from preconception to pregnancy, alongside declines in both screen and total sedentary behavior postpartum.
Unlike self-reported data, accelerometry captures the full spectrum of movement behaviors – including physical activity at varying intensities, sedentary time, and sleep – across the entire day. This comprehensive approach enables the examination of temporal variations in 24-h movement behaviors, such as weekday-weekend differences. Previous studies have reported mixed findings on weekday-weekend differences in maternal movement behaviors [25–27], but these primarily focused on parental behaviors rather than prospectively tracking changes from preconception through pregnancy and postpartum. Understanding weekday-weekend differences provides insight into how structured schedules (e.g., work, childcare) on weekdays contrast with the flexibility of weekends, enhancing the relevance of tailored interventions. Yet, weekday-weekend comparisons across the preconception-to-postpartum transition have not been thoroughly investigated.
This study aimed to describe the prospective changes in maternal 24-h movement behaviors (vigorous-, moderate-, light-intensity physical activity, sedentary behavior, and sleep) across preconception, mid-pregnancy, and postpartum; and comparing weekday and weekend differences of these behaviors. We hypothesized that (1) vigorous- and moderate-intensity physical activity would decline from preconception to pregnancy and remain low postpartum, (2) light-intensity activity would remain stable during pregnancy but increase postpartum, (3) sedentary behavior would increase during pregnancy and decrease postpartum, and (4) sleep duration would decline during pregnancy and further decrease postpartum. Further, we hypothesized that weekdays would show lower physical activity (of any intensity), higher sedentary behavior, and shorter sleep duration compared to weekends.
Methods
Study design and participants
The Singapore Preconception Study of Long-Term Maternal and Child Outcomes (S-PRESTO) is a prospective cohort study designed to investigate the impact of factors including nutrition, lifestyle, and maternal mood before and during pregnancy on offspring's epigenetics and health outcomes [28]. Briefly, from February 2015 to October 2017, 1,032 women aged 18–45 were enrolled, comprising Chinese, Malay, Indian, or mixed ethnicities, who were aiming to conceive and deliver in Singapore. After three preconception visits, those not achieving pregnancy within 12 months were withdrawn from the study (n = 557). For those who conceived (n = 475) and remained in the study and delivered a singleton (n = 373), further assessments were performed during and after gestation. Exclusion criteria included women who had been trying to conceive for over 18 months before recruitment; those currently pregnant, those who had used specific contraceptives or undergone fertility treatments in the past month, and those with health conditions including diabetes or taking systemic steroids, anticonvulsants, or recent medication for HIV or Hepatitis B/C. Written informed consent was provided by participants. Ethical approval was obtained from the SingHealth Centralised Institutional Review Board (reference 2014/692/D). This study is registered at ClinicalTrials.gov, NCT03531658 (registered May 22, 2018).
24-h movement behaviors
Participants were asked to wear ActiGraph wGT3X-BT accelerometers (ActiGraph, Pensacola, FL) to record their 24-h movement behaviors for seven consecutive days and nights (sampling rate of 80 Hz, based on its optimal balance between data resolution and storage efficiency [29, 30]) on their non-dominant wrist using the provided adjustable strap. Assessments were conducted during the first preconception clinic visit, the fourth pregnancy clinic visit at 24–28 weeks’ gestation, and the 12-month postpartum visit. To be valid for analysis, accelerometer data must include ≥ 16 h/day of wear time on at least three monitoring days (including at least one weekend day), consistent with wrist-worn accelerometer protocols from the UK Biobank cohort [31]. This approach ensures sufficient data capture while minimizing participant burden. Although shorter wear time thresholds (≥ 10 h) are common [32], the 16-h wear time threshold was applied to optimize data reliability without compromising participant compliance. Accelerometry raw data was processed with the R-package GGIR [33, 34]. Sustained inactivity and sleep windows were determined using the van Hees 2015 algorithm [35]. Non-sleep time was categorized into inactivity (acceleration threshold, < 25 milligravity [mg] of Euclidian Norm Minus One, 1 mg = 0.00981 m.s−2), light-intensity (25- < 100 mg), moderate-intensity (100- < 430 mg), and vigorous-intensity physical activity (≥ 430 mg) using prediction equations provided by Hildebrand et al. [36, 37] While inactivity resembles sedentary behavior, it is important to note that wrist-worn accelerometers cannot detect posture, which is a key aspect of defining sedentary behavior. Therefore, inactivity serves as a proxy for sedentary behaviors [37, 38], and the term “sedentary behavior” is consistently used throughout this article. To cover the entire 24-h movement spectrum, overall (non‐bouted) physical activity was the main outcome in the descriptive analyses. Additionally, to evaluate the impact of bout criteria on MVPA estimates, we conducted a supplementary analysis using a 1-min bout definition, where at least 80% of the time within each minute had to meet the 100 mg threshold criteria for MVPA [39].
Baseline sociodemographic and clinical characteristics
Baseline sociodemographic and clinical characteristics were collected at the first preconception clinic visit using an enrollment questionnaire. Data presented included age, ethnicity (Chinese, Malay, Indian, or mix/none of the above), highest education level (post-secondary and below, university degree, or professional/higher degree), employment status (unemployed or employed), and parity (nulliparous or primiparous/multiparous). Height was measured to the nearest 0.1 cm using a SECA 213 portable rangefinder, and weight was measured to the nearest 0.1 kg using a SECA 803 weighing machine. Body mass index (BMI) was calculated as weight (kg) divided by height (m2) and categorized using Asian-specific thresholds (underweight: < 18.5 kg/m2, normal weight: 18.5–22.9 kg/m2, overweight: 23.0–27.4 kg/m2, obese: ≥ 27.5 kg/m2). Underweight participants were grouped with normal weight in the analysis.
Statistical analysis
Statistical analyses were conducted using R version 4.3.1 (R Foundation for Statistical Computing, Vienna, Austria). Accelerometer-measured data were included if women had measurements across all three timepoints or at least two consecutive timepoints: 1) preconception and 24–28 weeks of pregnancy, or 2) 24–28 weeks pregnancy and 12 months postpartum. The assumption of data missing completely at random (MCAR) was assessed by comparing baseline characteristics of participants who contributed complete data to those with only preconception and mid-pregnancy data or only mid-pregnancy and postpartum data (as detailed in the Results section). Differences in continuous variables were evaluated using t-tests, while categorical variables were analyzed using chi-square tests or Fisher’s exact tests when expected cell counts were below five. Given that the assumption of MCAR appeared reasonable after this assessment, Generalized Estimating Equations (GEE) were used for the primary analysis to assess changes in movement behaviors across timepoints.
The three timepoints at preconception, mid-pregnancy, and postpartum were treated as repeated measures and coded as an ordinal variable (0, 1, and 2) using an unstructured correlation structure. The means and 95% confidence intervals (CI) of the variables were then reported for each timepoint. To assess whether there were differences in movement behaviors across timepoints, pairwise t-tests with a Bonferroni correction were conducted between timepoints 1 and 2, 1 and 3, and 2 and 3 after fitting the GEE model. A Wald test was performed for a global assessment of differences in movement behaviors across the entire study duration. Differences in movement behaviors between weekdays and weekends were assessed using pairwise t-tests with a Bonferroni correction for each timepoint separately by fitting the GEE model. Since our analysis focused on descriptive statistics to describe overall trends and changes across timepoints within the constant sample, adjustments for demographic variables were not included.
Results
The analysis included 139 women who provided data across either all three timepoints or for at least two consecutive time points (i.e., preconception-pregnancy or pregnancy-postpartum) and met the criteria of ≥ 16 h/day of data on at least two weekdays and one weekend day (Fig. 1). Participant baseline characteristics are presented in Table 1. The mean age was 30.8 years. Most women were underweight or of normal weight (61.9%), including 6.5% who were underweight and 55.4% who were of normal weight. The majority identified as Chinese (83.5%), held an undergraduate degree as their highest level of education (59.0%), were employed (88.5%), and were nulliparous (65.5%). Participants wore the accelerometer for an average of 7.4 (standard deviation [SD] 1.4), 7.5 (2.3), and 7.3 (1.2) valid days during preconception, mid-pregnancy, and postpartum, respectively (Table 2). Total waking wear time was consistent across timepoints, averaging 16.9 (SD 0.8), 16.8 (1.0), and 17.2 (1.0) hours/day. Supplementary Table 1 presents the assessment of whether data at different timepoints were MCAR. No differences were observed in all baseline characteristic—age, BMI, ethnicity, education level, employment status, or parity—between groups (all p > 0.05), supporting the MCAR assumption and justifying the use of GEE for our analysis.
Fig. 1.
Participants flow chart
Table 1.
Baseline characteristics of women included in the accelerometry study within the S-PRESTO cohort
| Baseline characteristics | n = 139 |
|---|---|
| Age (mean [SD], years) | 30.8 ± 3.5 |
| BMI, Asian cut-offs (n, %) | |
| Under & normal weight (< 23 kg/m2) | 86 (61.9) |
| Overweight (23–27.4 kg/m2) | 31 (22.3) |
| Obese (≥ 27.5 kg/m2) | 21 (15.1) |
| Missing | 1 (0.7) |
| Ethnicity (n, %) | |
| Chinese | 116 (83.5) |
| Malay | 14 (10.1) |
| Indian | 6 (4.3) |
| Mix/None of the above | 3 (2.2) |
| Highest level of education (n, %) | |
| Post-secondary and below | 35 (25.2) |
| University degree | 82 (59.0) |
| Professional/Higher degree | 22 (15.8) |
| Missing | 0 |
| Employment status (n, %) | |
| Unemployed | 16 (11.5) |
| Employed | 123 (88.5) |
| Missing | 0 |
| Parity (n, %) | |
| Nulliparous | 91 (65.5) |
| Primiparous/Multiparous | 48 (34.5) |
BMI body mass index, SD standard deviation
Table 2.
Valid wear days and total waking wear time across preconception, pregnancy, and postpartum
| Preconceptiona | Pregnancy | Postpartum | |
|---|---|---|---|
| Valid wear days, mean (SD) | 7.4 (1.4) | 7.5 (2.3) | 7.3 (1.2) |
| Total waking wear time, hours/day | 16.9 (0.8) | 16.8 (1.0) | 17.2 (1.0) |
SD standard deviation
aOnly those who eventually became pregnant were included
Overall, there were changes in all movement behaviors across the three timepoints (all p < 0.01, Fig. 2). Vigorous-intensity activity dropped from preconception (mean [95% CI]: 4.1 [2.8–5.4)] min/day) to mid-pregnancy (1.7 [0–4.2] min/day; p < 0.001 for preconception vs. mid-pregnancy) and remained low postpartum (1.8 [0–5.0] min/day, p = 0.918 vs. mid-pregnancy). Moderate-intensity activity also decreased from preconception (88.2 [82.8–93.5] min/day) to mid-pregnancy (68.7 [58.6–78.7] min/day; p < 0.001) but rebounded postpartum (90.2 [77.7–102.7] min/day; p < 0.001 vs. mid-pregnancy). Light-intensity activity remained stable from preconception (301.5 [289.6–313.5] min/day) to mid-pregnancy (298.3 [273.1–323.5] min/day, p = 0.629) but increased postpartum (340.1 [305.9–374.5] min/day; p = 0.001 vs. mid-pregnancy), exceeding preconception levels. Sedentary behavior increased from preconception (618.2 [603.4–633.1] min/day) to mid-pregnancy (639.6 [607.6–671.5] min/day; p = 0.029) and decreased postpartum (597.1 [553.5–640.7] min/day; p = 0.021 vs. mid-pregnancy), returning to preconception levels. Sleep duration remained stable from preconception (428.9 [420.6–437.3] min/day) to mid-pregnancy (432.2 [412.2–452.1] min/day; p = 0.586]) but decreased postpartum (408.4 [387.2–429.6] min/day; p = 0.004 vs. mid-pregnancy), falling below preconception levels.
Fig. 2.
Means and 95% CI for 24-h movement behaviors (min/day) across preconception, pregnancy, and postpartum (n = 139), and comparison across timepoints Mean and 95% CI were estimated using Generalized Estimating Equations (GEE). aPairwise comparisons between timepoints were conducted using t-tests with Bonferroni correction. bOverall change in means across all three timepoints was assessed using the Wald test. Note: MVPA (moderate-to-vigorous physical activity) is not presented in the figure, as it represents a combined measure of both moderate and vigorous intensity physical activity. Abbreviations: CI; confidence interval, MVPA; moderate-to-vigorous intensity physical activity
MVPA, a combination of vigorous- and moderate-intensity activity, though predominantly moderate, declined from preconception (91.9 [86.2–97.6] min/day) to mid-pregnancy (70.4 [60.0–80.9] min/day; p < 0.001 for preconception vs. mid-pregnancy) but rebounded postpartum (92.9 [79.8–105.9] min/day; p < 0.001 vs. mid-pregnancy), returning to preconception levels. When applying the 1-min bout definition (requiring 80% of each minute to meet the MVPA threshold), MVPA followed a similar trend but at lower absolute values: 33.3 (30.1–36.5), 21.9 (16.0–27.8), and 26.5 (19.6–33.3) min/day during preconception, mid-pregnancy and postpartum, respectively (Supplementary Fig. 1).
The daily distribution of 24-h movement behaviors analyzed by weekdays and weekends during each timepoint is illustrated in Fig. 3. No weekday-weekend differences in vigorous-intensity activity were observed (p > 0.05); percentages ranged from 0.1% to 0.3% of wear time. Although there was a general trend toward more moderate-intensity activity on weekends, the percentage distributions across weekdays and weekends were comparable at all three timepoints (preconception, mid-pregnancy, and postpartum) (p > 0.05), ranging from 4.7% to 6.6% of wear time. During both mid-pregnancy and postpartum phases, women spent more time engaging in light-intensity activity on weekends (21.3%–24.8%) compared to weekdays (20.5%–23.2%; p < 0.05). Across all three timepoints, women exhibited higher sedentary behavior during weekdays (42.5%–45.4%) compared to weekends (38.5%–42.1%; p < 0.001), while allocating more time to sleep during weekends (29.8%–32.0%) compared to weekdays (27.8%–29.3%; p < 0.01).
Fig. 3.
Percentage distribution of wear time across 24-h movement behaviors during preconception, pregnancy, and postpartum by weekdays and weekends (n = 139). * p < 0.05, ** p < 0.01, *** p < 0.001 denote statistical differences in 24-h movement behavior between weekdays and weekends across preconception, pregnancy, and postpartum
Discussion
This longitudinal study prospectively examined accelerometer-measured 24-h movement behaviors across preconception, mid-pregnancy, and 12-months postpartum in a multi-ethnic cohort in Singapore. Our findings partially supported the hypotheses: from preconception to mid-pregnancy, vigorous- and moderate-intensity activities decreased; however, in the postpartum period, while vigorous-intensity activity remained low, moderate-intensity activity rebounded, contrary to our expectation of persistent declines in both. Light-intensity activity remained unchanged from preconception to mid-pregnancy, as hypothesized, and increased postpartum. Sedentary behavior increased during mid-pregnancy and declined postpartum to preconception levels, aligning with our hypotheses. Sleep duration declined during pregnancy and further reduced postpartum, falling below preconception levels as predicted. For weekday-weekend differences, vigorous- and moderate-intensity activities unexpectedly showed no variation. While weekdays were associated with less light-intensity activity during mid-pregnancy and postpartum, weekends showed lower sedentary behavior and longer sleep duration across all timepoints, consistent with our hypotheses.
Few studies have examined physical activity changes from preconception to postpartum and early motherhood [15, 22–24], with most relying on self-reports. For example, a longitudinal study by Hesketh et al. [15] reported accelerometry data but only for early motherhood (4–7 years postpartum), with before/during pregnancy data being self-reported. Our accelerometer data revealed minimal vigorous-intensity activity at preconception (1.7 min/day) that persisted throughout mid-pregnancy and postpartum. This decline, though of uncertain clinical significance, represents a meaningful behavioral shift. Aligning with our findings, da Silva et al. [40] reported similarly low vigorous-intensity activity (3 min/day using a non-bouted criterion, and 1 min/day using a bout criterion of ≥ 1 min with 80% MVPA epochs). An earlier study from the National Health and Nutrition Examination Survey (NHANES) using waist-worn ActiGraph accelerometers reported even lower estimates of vigorous-intensity activity, with values ranging from 0.2–0.4 min/day (Troiano cut-points) and 0.3–0.7 min/day (Swartz cut-points) across trimesters [41]. These differences in estimates likely reflect the influence of methodological choices on activity quantification. Nevertheless, a previous review found that pregnant women who engaged in vigorous exercise 2–3 times per week were able to improve or maintain fitness without affecting pregnancy duration [42], highlighting a potential gap between recommendations (i.e., to maintain preconception activity levels) [6] and the observed decline during pregnancy. This decline may reflect concerns about physical discomfort, safety, or fetal impact [43, 44].
We observed a 19.5 min/day decline in moderate-intensity activity from preconception to mid-pregnancy. Our cohort showed higher MVPA estimates compared to previous studies with accelerometry measurements at two to three pregnancy timepoints –Whitaker et al. [45] (hip-worn ActiGraph): 43–52 min/day; Badon et al. [46]: 35–38 min/day; Sandborg et al. [47]: 18–32 min/day; and Kracht et al. [48]: 13–20 min/day. While wrist-worn monitors may yield higher counts than hip placement [36], our higher MVPA estimates primarily reflect the use of non-bouted processing criteria. Both da Silva et al. [40] and our study applied non-bouted and bouted criteria for comparison. Under non-bouted processing, da Silva et al. [40] reported > 90 min/day of MVPA in the second trimester, exceeding our non-bouted estimates (~ 70 min/day). With the bouted criteria (≥ 1 min with 80% of epochs ≥ MVPA cut-point), da Silva et al. [40] reported ~ 36 min/day of MVPA, which, while slightly higher, is in a comparable range to Kracht et al. [48] and our estimates (~ 22 min/day of bouted MVPA during mid-pregnancy). These results illustrate the impact of activity interruptions on MVPA quantification. Although we did not directly measure activity interruptions, transportation walking (which accounted for most MVPA in an adult population in prior research from Singapore [49]) may exemplify how bout criteria may underestimate MVPA. Brief interruptions (e.g., 30-s to 2-min pauses at traffic lights) could exclude otherwise valid MVPA minutes under an 80% bout threshold, despite participants engaging in predominantly moderate-intensity movement. In the present study, we aimed to report the full spectrum of activity, including sporadic bursts, to capture a more inclusive and ecologically valid representation of overall MVPA, reflecting the inherent variability of free-living activity patterns. Beyond bout criteria, different intensity thresholds also influence MVPA estimates. Compared to our study’s thresholds, newer intensity thresholds by Mielke et al. [50] (e.g., ≥ 25 mg for light, ≥ 78 mg for moderate, ≥ 249 mg for vigorous) may yield higher estimates of physical activity and correspondingly lower sedentary time. These data further demonstrate the influence of methodological choices on accelerometry estimates, which may subsequently affect evaluations of health outcomes and physical activity recommendations.
Notably, while MVPA exceeded the ≥ 150 min/week guideline [6] at all timepoints, this likely reflects methodological differences: the guideline is based on self-reported, bouted activity [51], whereas our accelerometry captured both sustained and sporadic MVPA. Discrepancies between device-measured and self-reported activity are well-documented [52, 53], underscoring the need to refine guidelines to better integrate device-based evidence [51]. Given these differences, we did not directly convert daily MVPA values to weekly totals, maintaining data granularity and avoiding assumptions of consistent activity patterns across days. Despite methodological variations, all previous studies reported declines in physical activity, regardless of intensity, from preconception to pregnancy [15, 22, 23]. During postpartum, while the observed rebound in moderate-intensity activity is encouraging, these levels returned to those observed during preconception. Randomized trials showed that moderate- or vigorous-intensity activity during pregnancy does not harm pregnancy progression or offspring health [54–56]. Interventions promoting awareness and adherence to guidelines are needed to support optimal activity levels throughout pregnancy and beyond.
Light-intensity physical activity remained stable from preconception to mid-pregnancy, only partially offsetting the decline in moderate-intensity activity. This stability, combined with increased mid-pregnancy sedentary behavior, implies replacement of higher-intensity with lower-intensity movement. Our light-intensity activity estimates during pregnancy exceeded those of McParlin et al. [57] (120–122 min/day across trimesters) and Sandborg et al. [47] (198–210 min/day at 14–37 gestational weeks) but were lower than Badon et al. [46] (384–408 min/day, early-late pregnancy). Methodological, temporal, and population differences may explain these variations. Postpartum, light-intensity activity increased, replacing some sedentary time and aligning with WHO recommendations for health [6]. This rise mirrored Kracht et al. [48] (~ 160 min/day during pregnancy; 196 min/day postpartum).
In this study, sedentary behavior increased by an average of 21.4 min/day from preconception to mid-pregnancy. However, at 12 months postpartum, it returned to near preconception levels, reflecting a decrease of 42.5 min/day from mid-pregnancy. Compared to our estimates, Badon et al. [46] reported lower sedentary behavior during pregnancy (532–536 min/day), and McParlin et al. [57] observed median sedentary time ranging from 585–631 min/day across trimesters. Whitaker et al. [45] reported higher sedentary time across trimesters: 936 min/day (first), 907 min/day (second), and 912 min/day (third). Kracht et al. [48] found a similar trajectory, with sedentary time increasing from 618 min/day in early pregnancy to 630 min/day in late pregnancy, then decreasing to 588 min/day at 1 year postpartum, closely aligning with our findings. These variations, along with the generally higher sedentary time observed in device-based studies compared to self-reported measures [15, 23], highlight the methodological and population-level differences influencing sedentary behavior estimates.
Accelerometer-measured sleep duration in our study remained stable from preconception to mid-pregnancy, contrasting with previous research reporting declines in self-reported sleep duration beginning in the second trimester [58, 59]. This discrepancy may stem from retrospective recall method of data collection [58]. Our assessment period, which occurred during the second trimester, captured a time when sleep quality begins to decline but may not yet reach the levels of disruption as seen more commonly in the third trimester [60]. A meta-analysis [61] of 16 actigraphy studies, most of which assessed the third trimester, found a 10.8% decline in sleep duration from pregnancy to 6 months postpartum. In contrast, our study observed a smaller reduction of 5.5% in sleep duration (equivalent to 23.8 min/day) from mid-pregnancy, which persisted up to 12 months postpartum. Mothers in our study averaged 7.2 h/day of sleep during mid-pregnancy, but this decreased to 6.8 h/day postpartum—4.8% (20.5 min/day) lower than preconception levels. Notably, this 4.8% reduction at 12 months postpartum may underestimate sleep disruption earlier in the postpartum period, as infant sleep schedules are often less established in the first few months [62]. Future research may include assessments across the postpartum period (e.g., 3, 6, and 9 months) to better capture dynamic changes in sleep and activity patterns. Interventions addressing maternal sleep are crucial to prevent worsening sleep problems over time.
While no significant weekday-weekend differences were found for vigorous- or moderate-intensity activity at any timepoint, there was an overall trend of increased physical activities on weekends. Light-intensity activity levels were higher on weekends compared to weekdays during mid-pregnancy and postpartum. On weekends, sedentary behavior was consistently lower across all timepoints, while sleep duration was consistently higher. These patterns suggest weekends favor more light-intensity activity and longer sleep, whereas weekdays are marked by higher sedentary behavior. To our knowledge, no studies have specifically examined weekday-weekend differences in 24-h movement behaviors among mothers for direct comparison. Nonetheless, several device-based studies on parent–child behaviors have been identified, reporting mixed findings: some found higher physical activity on weekends [25], while others reported lower activity, [26] reduced step counts [27], or increased sedentary behavior [26]. These inconsistencies highlight the need for further research on weekday-weekend differences in maternal movement behaviors across the preconception-to-postpartum transition—an area that remains underexplored. Future research could explore the specific activities driving these patterns and their potential implications for maternal and offspring health. Interventions might focus on promoting structured activities (e.g., active commuting) during weekdays and encouraging family-based activities (e.g., park visits) on weekends to support healthier movement behaviors [63].
Strengths and limitations
Strengths of our study include its longitudinal, prospective analysis of maternal 24-h movement behaviors, capturing temporal variations across preconception, mid-pregnancy, and postpartum. The exploration of weekday-weekend variations added nuance by considering potential lifestyle differences, while accelerometry enhanced reliability and minimized social desirability bias inherent in self-reports. Additionally, our study is among the first to use accelerometry to prospectively track 24-h movement behaviors from preconception, providing a comprehensive understanding of their evolution across key reproductive stages.
Some limitations should be noted. Our study population may not represent the broader Singaporean female population, particularly those who have not experienced pregnancy, limiting generalizability. While alternative processing methods, such as those proposed by Mielke et al. [50], would yield different absolute estimates of activity volumes, the temporal trends (e.g. the observed decline in moderate-intensity activity from preconception to pregnancy) we observed would likely remain consistent. Nevertheless, our findings should be interpreted in the context of the specific intensity cut-points and bout criteria employed. Accelerometry data did not differentiate between leisure and occupational physical activity, which may have distinct health implications [64–66], a limitation common in accelerometry studies. While data collection over seven consecutive days is widely employed, the dynamic changes across the entirety of the preconception, pregnancy, and postpartum periods were not fully captured. Requiring only one weekend day for valid accelerometry data may limit the representativeness of weekend movement patterns. The study also did not capture factors influencing weekend activity patterns, such as work schedules or childcare responsibilities. The lack of sleep diaries or non-wear logs may have led to misclassification of sleep and wake periods, potentially impacting the accuracy of accelerometer-derived sleep estimates. However, given that the accelerometer was wrist-worn, it is unlikely participants remained completely still for > 15 min during wakefulness, as even sedentary activities (e.g., sitting, working) typically involve intermittent wrist movements. Wrist-worn accelerometers are also well-validated for detecting sleep–wake patterns [35].
Future research should assess adherence to 24-h movement profiles (currently adult-only) for pregnancy monitoring and develop pregnancy-specific 24-h movement guidelines, integrating physical activity, sedentary behavior, and sleep quality (beyond duration) to optimize maternal and fetal health. The variability in processing criteria highlights the need for continued development of standardized accelerometry thresholds and device-based physical activity recommendations to improve classification consistency, facilitate cross-study comparisons, and advance our understanding of physical activity patterns. Incorporating sleep logs, assessing movement behaviors across all trimesters, and exploring paid leave policies as a covariate could provide a more comprehensive understanding of activity patterns during pregnancy and postpartum. Interventions should address barriers such as physical discomfort, childcare responsibilities, and work schedules, while policymakers could promote workplace flexibility and paid leave to support maternal health. These efforts would address current guideline limitations and enhance the relevance of 24-h movement behaviors research.
Conclusions
During pregnancy, vigorous- and moderate-intensity activity declined, with vigorous-intensity activity remaining low postpartum. Light-intensity activity increased postpartum, while sedentary behavior increased during pregnancy. Sleep duration decreased postpartum. Vigorous- and moderate-intensity activity showed no weekday-weekend differences. Weekdays were marked by less light-intensity activity during pregnancy and postpartum and higher sedentary behavior across all timepoints, while weekends had more sleep across timepoints. These findings highlight key targets for improving maternal health: promoting vigorous- and moderate-intensity activity during pregnancy and beyond, reducing sedentary time on weekdays, and supporting light-intensity activity and sleep, particularly on weekdays.
Supplementary Information
Acknowledgements
We sincerely thank the study participants and S-PRESTO study group.
Clinical trial information
ClinicalTrials.gov, NCT03531658 (registered May 22, 2018).
Authors’ contributions
Research design, data interpretation, and manuscript revision: AHYC, NP, JYB, FMR. Literature review, data analysis, and manuscript writing: AHYC. S-PRESTO cohort study: YSC, LPS, KHT, PDG, FKPY, YSL, JKYC, KMG, SYC. Data acquisition: AHYC, NP, SLT, CMJLG. Manuscript revision: CMJLG, KHT, YSL, SLL, KMG, JGE, SYC. Reading and approval of the final manuscript: All authors.
Funding
This research was supported by the Singapore National Research Foundation under its Translational and Clinical Research (TCR) Flagship Programme and administered by the Singapore Ministry of Health’s National Medical Research Council (NMRC), Singapore- NMRC/TCR/004-NUS/2008; NMRC/TCR/012-NUHS/2014. The Singapore Lipidomics Incubator (SLING) is supported by grants from the National University of Singapore via the Life Sciences Institute, the Singapore National Research Foundation (NRF, NRFI2015-05, and NRFSBP-P4), and A*STAR IAF-ICP I1901E0040. Additional funding is provided by the Singapore Institute for Clinical Sciences (SICS) – Agency for Science, Technology and Research (A*STAR), Singapore.
Data availability
The dataset supporting the conclusions of this article can be made available upon request and after approval by the S-PRESTO Executive Committee.
Declarations
Ethics approval and consent to participate
Ethical approval for this study was obtained from the SingHealth Centralised Institutional Review Board (reference 2014/692/D). This study is registered at ClinicalTrials.gov (NCT 03531658). All participants provided informed consent prior to participation.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Rollo S, Antsygina O, Tremblay MS. The whole day matters: understanding 24-hour movement guideline adherence and relationships with health indicators across the lifespan. J Sport Health Sci. 2020;9(6):493–510. 10.1016/j.jshs.2020.07.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Ross R, Chaput JP, Giangregorio LM, et al. Canadian 24-hour movement guidelines for adults aged 18–64 years and adults aged 65 years or older: an integration of physical activity, sedentary behaviour, and sleep. Appl Physiol Nutr Metab. 2020;45(10 (Suppl. 2)):S57–102. 10.1139/apnm-2020-0467. [DOI] [PubMed] [Google Scholar]
- 3.Chauhan G, Tadi P. Physiology, postpartum changes. StatPearls. Treasure Island (FL): StatPearls Publishing; 2022. https://www.ncbi.nlm.nih.gov/books/NBK555904/. Accessed 27 Feb 2025. [PubMed] [Google Scholar]
- 4.Kepley J, Bates K, Mohiuddin S. Physiology, maternal changes. StatPearls. Treasure Island (FL): StatPearls Publishing; 2023. https://www.ncbi.nlm.nih.gov/books/NBK539766/. Accessed 27 Feb 2025. [PubMed] [Google Scholar]
- 5.Guthold R, Stevens GA, Riley LM, Bull FC. Worldwide trends in insufficient physical activity from 2001 to 2016: a pooled analysis of 358 population-based surveys with 1.9 million participants. Lancet Glob Health. 2018;6(10):e1077–86. 10.1016/S2214-109X(18)30357-7. [DOI] [PubMed] [Google Scholar]
- 6.World Health Organization. WHO guidelines on physical activity and sedentary behaviour. World Health Organization. Geneva, Switzerland. 2020.
- 7.Harrison CL, Brown WJ, Hayman M, Moran LJ, Redman LM. The role of physical activity in preconception, pregnancy and postpartum health. Semin Reprod Med. 2016;34(2):e28–37. 10.1055/s-0036-1583530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Gascoigne EL, Webster CM, Honart AW, Wang P, Smith-Ryan A, Manuck TA. Physical activity and pregnancy outcomes: an expert review. Am J Obstet Gynecol MFM. 2023;5(1):100758. 10.1016/j.ajogmf.2022.100758. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Osumi A, Kanejima Y, Ishihara K, et al. Effects of sedentary behavior on the complications experienced by pregnant women: a systematic review. Reprod Sci. 2024;31(2):352–65. 10.1007/s43032-023-01321-w. [DOI] [PubMed] [Google Scholar]
- 10.Wallace MK, Jones MA, Whitaker K, Barone Gibbs B. Patterns of physical activity and sedentary behavior before and during pregnancy and cardiometabolic outcomes. Midwifery. 2022;114:103452. 10.1016/j.midw.2022.103452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Nevarez-Brewster M, Han D, Todd EL, Keim P, Doom JR, Davis EP. Sleep during pregnancy and offspring outcomes from infancy to childhood: a systematic review. Psychosom Med. 2025;87(1):7–32. 10.1097/PSY.0000000000001352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Román-Gálvez MR, Amezcua-Prieto C, Salcedo-Bellido I, et al. Physical activity before and during pregnancy: a cohort study. Int J Gynecol Obstet. 2021;152(3):374–81. 10.1002/ijgo.13387. [DOI] [PubMed] [Google Scholar]
- 13.Badon SE, Littman AJ, Chan KCG, Williams MA, Enquobahrie DA. Maternal sedentary behavior during pre-pregnancy and early pregnancy and mean offspring birth size: a cohort study. BMC Pregnancy Childbirth. 2018;18(1):267. 10.1186/s12884-018-1902-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Amezcua-Prieto C, Olmedo-Requena R, Jímenez-Mejías E, et al. Changes in leisure time physical activity during pregnancy compared to the prior year. Matern Child Health J. 2013;17(4):632–8. 10.1007/s10995-012-1038-3. [DOI] [PubMed] [Google Scholar]
- 15.Hesketh KR, Baird J, Crozier SR, et al. Activity behaviors before and during pregnancy are associated with women’s device-measured physical activity and sedentary time in later parenthood: a longitudinal cohort analysis. J Phys Act Health. 2023;20(9):803–11. 10.1123/jpah.2022-0630. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Pereira MA, Rifas-Shiman SL, Kleinman KP, Rich-Edwards JW, Peterson KE, Gillman MW. Predictors of change in physical activity during and after pregnancy: project Viva. Am J Prev Med. 2007;32(4):312–9. 10.1016/j.amepre.2006.12.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Borodulin K, Evenson KR, Herring AH. Physical activity patterns during pregnancy through postpartum. BMC Womens Health. 2009;9(1):32. 10.1186/1472-6874-9-32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Hesketh KR, Evenson KR, Stroo M, Clancy SM, Østbye T, Benjamin-Neelon SE. Physical activity and sedentary behavior during pregnancy and postpartum, measured using hip and wrist-worn accelerometers. Prev Med Rep. 2018;10:337–45. 10.1016/j.pmedr.2018.04.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Padmapriya N, Shen L, Soh SE, et al. Physical activity and sedentary behavior patterns before and during pregnancy in a multi-ethnic sample of Asian women in Singapore. Matern Child Health J. 2015;19(11):2523–35. 10.1007/s10995-015-1773-3. [DOI] [PubMed] [Google Scholar]
- 20.Richardsen KR, Mdala I, Berntsen S, et al. Objectively recorded physical activity in pregnancy and postpartum in a multi-ethnic cohort: association with access to recreational areas in the neighbourhood. Int J Behav Nutr Phys Act. 2016;13(1):78. 10.1186/s12966-016-0401-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Mielke GI, Crochemore-Silva I, Domingues MR, Silveira MF, Bertoldi AD, Brown WJ. Physical activity and sitting time from 16 to 24 weeks of pregnancy to 12, 24, and 48 months postpartum: findings from the 2015 Pelotas (Brazil) birth cohort study. J Phys Act Health. 2021;18(5):587–93. 10.1123/jpah.2020-0351. [DOI] [PubMed] [Google Scholar]
- 22.Tornquist L, Tornquist D, Mielke GI, da Silveira MF, Hallal PC, Domingues MR. Maternal physical activity patterns in the 2015 pelotas birth cohort: from preconception to postpartum. J Phys Act Health. 2023;20(9):868–77. 10.1123/jpah.2022-0609. [DOI] [PubMed] [Google Scholar]
- 23.Chu AHY, Padmapriya N, Tan SL, et al. Longitudinal analysis of patterns and correlates of physical activity and sedentary behavior in women from preconception to postpartum: the Singapore Preconception Study of Long-Term Maternal and Child Outcomes cohort. J Phys Act Health. 2023;20(9):850–9. 10.1123/jpah.2022-0642. [DOI] [PubMed] [Google Scholar]
- 24.Sjögren Forss K, Stjernberg L. Physical activity patterns among women and men during pregnancy and 8 months postpartum compared to pre-pregnancy: a longitudinal study. Front Public Health. 2019;7:294. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Prioreschi A, Brage S, Westgate K, Micklesfield LK. Describing the diurnal relationships between objectively measured mother and infant physical activity. Int J Behav Nutr Phys Act. 2018;15(1):59. 10.1186/s12966-018-0692-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Fuemmeler BF, Anderson CB, Mâsse LC. Parent-child relationship of directly measured physical activity. Int J Behav Nutr Phys Act. 2011;8(1):17. 10.1186/1479-5868-8-17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Sigmundová D, Sigmund E, Badura P, Vokáčová J, Trhlíková L, Bucksch J. Weekday-weekend patterns of physical activity and screen time in parents and their pre-schoolers. BMC Public Health. 2016;16(1):898. 10.1186/s12889-016-3586-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Loo EXL, Soh SE, Loy SL, et al. Cohort profile: Singapore preconception study of long-term maternal and child outcomes (S-PRESTO). Eur J Epidemiol. 2021;36(1):129–42. 10.1007/s10654-020-00697-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.John D, Sasaki J, Staudenmayer J, Mavilia M, Freedson P. Comparison of raw acceleration from the GENEA and ActiGraph™ GT3X+ activity monitors. Sensors. 2013;13(11):14754–63. 10.3390/s131114754. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.ActiGraph LLC. User Guide: ActiGraph wGT3X-BT + ActiLife. Activity Monitor: ActiGraph wGT3X-BT | E.200.6003 | Revision: 8 | Released: 03/22/2024. 2024. https://6407355.fs1.hubspotusercontent-na1.net/hubfs/6407355/User%20Manuals/ActiGraph_wGT3X-BT_UserGuide_E.200.6003_Revision7.pdf. Accessed 28 Feb 2025.
- 31.Stamatakis E, Ahmadi MN, Friedenreich CM, et al. Vigorous intermittent lifestyle physical activity and cancer incidence among nonexercising adults. JAMA Oncol. 2023;9(9):1255. 10.1001/jamaoncol.2023.1830. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Giurgiu M, Timm I, Becker M, et al. Quality evaluation of free-living validation studies for the assessment of 24-hour physical behavior in adults via wearables: systematic review. JMIR Mhealth Uhealth. 2022;10(6):e36377. 10.2196/36377. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Migueles JH, Rowlands AV, Huber F, Sabia S, van Hees VT. GGIR: a research community-driven open source R package for generating physical activity and sleep outcomes from multi-day raw accelerometer data. J Meas Phys Behav. 2019;2(3):188–96. 10.1123/jmpb.2018-0063. [Google Scholar]
- 34.van Hees VT, Gorzelniak L, Dean León EC, et al. Separating movement and gravity components in an acceleration signal and implications for the assessment of human daily physical activity. PLoS One. 2013;8(4):e61691. 10.1371/journal.pone.0061691. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.van Hees VT, Sabia S, Anderson KN, et al. A novel, open access method to assess sleep duration using a wrist-worn accelerometer. PLoS One. 2015;10(11):e0142533. 10.1371/journal.pone.0142533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Hildebrand M, Van Hees VT, Hansen BH, Ekelund U. Age group comparability of raw accelerometer output from wrist- and hip-worn monitors. Med Sci Sports Exerc. 2014;46(9):1816–24. 10.1249/MSS.0000000000000289. [DOI] [PubMed] [Google Scholar]
- 37.Hildebrand M, Hansen BH, van Hees VT, Ekelund U. Evaluation of raw acceleration sedentary thresholds in children and adults. Scand J Med Sci Sports. 2017;27(12):1814–23. 10.1111/sms.12795. [DOI] [PubMed] [Google Scholar]
- 38.Tremblay MS, Aubert S, Barnes JD, et al. Sedentary Behavior Research Network (SBRN) - terminology consensus project process and outcome. Int J Behav Nutr Phys Act. 2017;14(1):75. 10.1186/s12966-017-0525-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.da Silva IC, van Hees VT, Ramires VV, et al. Physical activity levels in three Brazilian birth cohorts as assessed with raw triaxial wrist accelerometry. Int J Epidemiol. 2014;43(6):1959–68. 10.1093/ije/dyu203. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.da Silva SG, Evenson KR, da Silva ICM, et al. Correlates of accelerometer-assessed physical activity in pregnancy—the 2015 Pelotas (Brazil) birth cohort study. Scand J Med Sci Sports. 2018;28(8):1934–45. 10.1111/sms.13083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Evenson KR, Wen F. Prevalence and correlates of objectively measured physical activity and sedentary behavior among US pregnant women. Prev Med Baltim. 2011;53(1):39–43. 10.1016/j.ypmed.2011.04.014. [DOI] [PubMed] [Google Scholar]
- 42.Kramer MS, McDonald SW. Aerobic exercise for women during pregnancy. Cochrane Database Syst Rev. 2006. 10.1002/14651858.CD000180.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Ferrari N, Joisten C. Impact of physical activity on course and outcome of pregnancy from pre- to postnatal. Eur J Clin Nutr. 2021. 10.1038/s41430-021-00904-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Coll CVN, Domingues MR, Gonçalves H, Bertoldi AD. Perceived barriers to leisure-time physical activity during pregnancy: a literature review of quantitative and qualitative evidence. J Sci Med Sport. 2017;20(1):17–25. 10.1016/j.jsams.2016.06.007. [DOI] [PubMed] [Google Scholar]
- 45.Whitaker KM, Zhang D, Kline CE, Catov J, Barone Gibbs B. Associations of sleep with sedentary behavior and physical activity patterns across pregnancy trimesters. Womens Health Issues. 2021;31(4):366–75. 10.1016/j.whi.2021.02.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Badon SE, Ferrara A, Gabriel KP, Avalos LA, Hedderson MM. Changes in 24-hour movement behaviors from early to late pregnancy in individuals with prepregnancy overweight or obesity. J Phys Act Health. 2022;19(12):842–6. 10.1123/jpah.2022-0333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Sandborg J, Migueles JH, Söderström E, Blomberg M, Henriksson P, Löf M. Physical activity, body composition, and cardiometabolic health during pregnancy: a compositional data approach. Med Sci Sports Exerc. 2022. 10.1249/MSS.0000000000002996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Kracht CL, Drews KL, Flanagan EW, et al. Maternal 24-h movement patterns across pregnancy and postpartum: The LIFE-Moms consortium. Prev Med Rep. 2024;42:102740. 10.1016/j.pmedr.2024.102740. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Chu AHY, Ng SHX, Koh D, Müller-Riemenschneider F. Reliability and validity of the self- and interviewer-administered versions of the Global Physical Activity Questionnaire (GPAQ). PLoS One. 2015;10(9):e0136944–e0136944. 10.1371/journal.pone.0136944. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Mielke GI, de Almeida MM, Ekelund U, Rowlands AV, Reichert FF, Crochemore-Silva I. Absolute intensity thresholds for tri-axial wrist and waist accelerometer-measured movement behaviors in adults. Scand J Med Sci Sports. 2023;33(9):1752–64. 10.1111/sms.14416. [DOI] [PubMed] [Google Scholar]
- 51.Troiano RP, Stamatakis E, Bull FC. How can global physical activity surveillance adapt to evolving physical activity guidelines? Needs, challenges and future directions. Br J Sports Med. 2020;54(24):1468–73. 10.1136/bjsports-2020-102621. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Prince SA, Adamo KB, Hamel M, Hardt J, Connor Gorber S, Tremblay M. A comparison of direct versus self-report measures for assessing physical activity in adults: a systematic review. Int J Behav Nutr Phys Act. 2008;5(1):56. 10.1186/1479-5868-5-56. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Prince SA, Cardilli L, Reed JL, et al. A comparison of self-reported and device measured sedentary behaviour in adults: a systematic review and meta-analysis. Int J Behav Nutr Phys Act. 2020;17(1):31. 10.1186/s12966-020-00938-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Xie Y, Zhao H, Zhao M, et al. Effects of resistance exercise on blood glucose level and pregnancy outcome in patients with gestational diabetes mellitus: a randomized controlled trial. BMJ Open Diabetes Res Care. 2022;10(2).10.1136/bmjdrc-2021-002622. [DOI] [PMC free article] [PubMed]
- 55.Ruchat S-M, Davenport MH, Giroux I, et al. Effect of exercise intensity and duration on capillary glucose responses in pregnant women at low and high risk for gestational diabetes. Diabetes Metab Res Rev. 2012;28(8):669–78. 10.1002/dmrr.2324. [DOI] [PubMed] [Google Scholar]
- 56.Petrov Fieril K, Glantz A, Fagevik Olsen M. The efficacy of moderate-to-vigorous resistance exercise during pregnancy: a randomized controlled trial. Acta Obstet Gynecol Scand. 2015;94(1):35–42. 10.1111/aogs.12525. [DOI] [PubMed] [Google Scholar]
- 57.McParlin C, Robson SC, Tennant PW, et al. Objectively measured physical activity during pregnancy: a study in obese and overweight women. BMC Pregnancy Childbirth. 2010;10(1):76. 10.1186/1471-2393-10-76. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Hedman C, Pohjasvaara T, Tolonen U, Suhonen-Malm AS, Myllylä VV. Effects of pregnancy on mothers’ sleep. Sleep Med. 2002;3(1):37–42. 10.1016/S1389-9457(01)00130-7. [DOI] [PubMed] [Google Scholar]
- 59.Lucchini M, O’Brien LM, Kahn LG, et al. Racial/ethnic disparities in subjective sleep duration, sleep quality, and sleep disturbances during pregnancy: an ECHO study. Sleep. 2022;45(9).10.1093/sleep/zsac075. [DOI] [PMC free article] [PubMed]
- 60.Mislu E, Kumsa H, Tadesse S, et al. Sleep quality disparities in different pregnancy trimesters in low- and middle-income countries: a systematic review and meta-analysis. BMC Pregnancy Childbirth. 2024;24(1):627. 10.1186/s12884-024-06830-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Parsons L, Howes A, Jones CA, Surtees ADR. Changes in parental sleep from pregnancy to postpartum: a meta-analytic review of actigraphy studies. Sleep Med Rev. 2023;68:101719. 10.1016/j.smrv.2022.101719. [DOI] [PubMed] [Google Scholar]
- 62.Bruni O, Baumgartner E, Sette S, et al. Longitudinal study of sleep behavior in normal infants during the first year of life. J Clin Sleep Med. 2014;10(10):1119–27. 10.5664/jcsm.4114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Arab A, Karimi E, Garaulet M, Scheer FAJL. Social jetlag and obesity: a systematic review and meta‐analysis. Obesity Rev. 2024;25(3).10.1111/obr.13664. [DOI] [PMC free article] [PubMed]
- 64.Chu AHY, Moy FM. Associations of occupational, transportation, household and leisure-time physical activity patterns with metabolic risk factors among middle-aged adults in a middle-income country. Prev Med (Baltim). 2013;57:S14–7. 10.1016/j.ypmed.2012.12.011. [DOI] [PubMed] [Google Scholar]
- 65.Chu AHY, van Dam RM, Biddle SJH, Tan CS, Koh D, Müller-Riemenschneider F. Self-reported domain-specific and accelerometer-based physical activity and sedentary behaviour in relation to psychological distress among an urban Asian population. Int J Behav Nutr Phys Act. 2018;15(1):36. 10.1186/s12966-018-0669-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Bonekamp NE, Visseren FLJ, Ruigrok Y, et al. Leisure-time and occupational physical activity and health outcomes in cardiovascular disease. Heart. 2023;109(9):686–94. 10.1136/heartjnl-2022-321474. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The dataset supporting the conclusions of this article can be made available upon request and after approval by the S-PRESTO Executive Committee.



