Abstract
Background
Physical inactivity, sedentary behaviour and inadequate sleep are established risk factors for non-communicable diseases. Although older adults are traditionally expected to be less active and more sedentary than young adults, contemporary social, occupational and educational environments may have changed this. Here, we characterised 24-hour movement behaviours (physical activity [PA], sedentary behaviour [SB], and sleep) across adulthood using wearable devices and examined their cardiometabolic correlates using a compositional data approach.
Methods
Data were analysed from 1,967 adults across three Singaporean cohorts: university students (n = 500; mean[SD] age 19.9[1.3] years), working-age adults (n = 437; 41.1[10.0] years), and community-dwelling older adults (n = 1,030; 74.0[2.6] years). Each person contributed 4 weeks of Oura Ring recordings on time spent in PA, SB and sleep. BMI, body roundness index (BRI), pulse wave velocity (PWV), and a composite vascular health score (zComposite) were additionally assessed. Associations between reallocations of time across 24 h-movement behaviours and these cardiometabolic outcomes were estimated using compositional data regression models.
Results
University students accumulated the most SB (mean 633.89 min/day) and the lowest PA (320.28 min/day) and sleep (431.75 min/day), whereas older adults accumulated the least SB (500.86 min/day) and greatest PA (420.28 min/day) and sleep (455.62 min/day). Working-age adults showed profiles in-between the students and older adults (SB: 581.28 min/day; PA: 346.55 min/day; sleep: 445.77 min/day). In compositional models, reallocating 30 min per day to PA from other behaviours was associated with lower BMI (-0.13 kg/m²), BRI (-0.04), PWV (-0.05 m/s), and zComposite (-0.01). Reallocating 30 min per day from SB to other behaviours was associated with lower BMI (-0.28 kg/m²) and BRI (-0.07). Reallocating 30 min per day to sleep from other behaviours was related to lower BMI (-0.21 kg/m2) and BRI (-0.05).
Conclusions
University students exhibited lower physical activity and higher sedentary time than older adults. Reallocation of time toward greater PA, less SB and longer sleep was associated with lower cardiometabolic risk. These findings challenge conventional expectations about age-related inactivity and highlight young adulthood as a critical, under-recognised target for interventions to promote PA and reduce SB for long-term health.
Supplementary Information
The online version contains supplementary material available at https://doi.org/10.1186/s12916-026-05192-1.
Keywords: Physical activity, Sedentary behaviour, Sleep, Compositional data analysis, Wearable devices, Obesity, Arterial Stiffness
Background
Physical inactivity and excessive sedentary behaviour are two leading modifiable risk factors for non-communicable diseases (NCDs) worldwide, contributing substantially to premature mortality and morbidity from cardiovascular disease, type 2 diabetes and obesity [1, 2]. Global estimates suggest that insufficient physical activity accounts for more than 5 million deaths annually [1]. Sedentary behaviour – although related to inactivity, is now recognised as a distinct construct referring to waking behaviours with low energy expenditure, and has been shown to be an independent predictor of cardiometabolic risk beyond physical inactivity [3, 4].
Physical activity has traditionally followed a predictable life-course trajectory: high levels of movement in childhood and early adult life, plateauing during working life and then declining in later years as a result of increased frailty, accumulation of chronic disease, and progressive functional limitations [5–7]. Sedentary behaviours, although generally high in older age [8] tend to peak in working-age adults who have prolonged sitting and commuting demands. This conceptual model, whereby physical activity declines with age while sedentary behaviour peaks in midlife or later, is supported by epidemiological data up until the early 21st century [5–8] and has shaped public health promotion efforts. Whether this life-course trajectory still holds true is of interest.
A third movement behaviour that occupies a significant portion of the 24 h day is sleep. Short sleep has also been consistently linked to increased obesity levels [9–11], insulin resistance [12, 13], and cardiovascular risk [14, 15]. In light of these findings, the American Heart Association added sleep health as the 8th component of its cardiovascular health construct in 2022, acknowledging this as a much broader construct than just the absence of disease [16].
Technological advances in modern society have fostered round-the-clock, global connectivity – be it in study, work or leisure settings. These factors simultaneously decrease time available for physical activity and sleep, while increasing time spent in sedentary behaviours. As such, recent studies have shifted the field away from examining these movement behaviours in isolation, towards recognising these as mutually dependent parts of a finite 24 h day [17]. Using compositional data analysis, early work by Chastin et al. showed that the overall distribution of sleep, sedentary time, light physical activity, and moderate-to-vigorous physical activity (MVPA) was associated with BMI, waist circumference, triglycerides, glucose, and insulin, with the most favourable cardiometabolic profiles generally observed when more time was allocated to MVPA and less to sedentary behaviour [18]. Subsequent studies in adults support these findings, showing that greater relative time in MVPA is associated with lower adiposity, healthier lipid profiles, better cardiorespiratory fitness, and more favourable cardiometabolic risk scores, while sedentary time tends to show adverse associations [19].
However, several gaps remain. Much of the existing evidence is cross-sectional, self-report, derived from Western cohorts, and focused on middle-aged or older adults with richer cardiometabolic phenotyping. Individual studies across multiple countries have shown dramatic declines in physical activity in children and adolescents alongside early and rapid increase in screen time [20, 21], signalling the importance of examining movement behaviours in younger age groups. Studies directly comparing movement behaviour compositions across adult life stages using harmonised objective/wearable-based measures remain uncommon. In addition, relatively few studies have examined both obesity-related and vascular outcomes within the same analytical framework.
Toward these ends, we investigated 24 h movement behaviours across three independent samples in Singapore: university students (18-25y), working-age adults (23-67y), and community-dwelling older adults (67-80y), who were provided with wearable devices. We further analysed how the allocation of physical activity, sedentary time and sleep relate to established cardiometabolic markers of obesity and arterial stiffness [22] within the same, 24-composition analytical framework.
Methods
Study design and participants
This analysis draws on data from three independent Singapore-based cohort studies. University students from the National University of Singapore (n = 638) took part in the NUS1000 Study [23]; working adults employed by the National University of Singapore (n = 575) took part in the NUS1000 Staff Edition Study; while older adults (n = 1,205) were drawn from the SG70 cohort [24]. Details of inclusion and exclusion criteria for each study have been described in previous publications [23, 24] and are also provided in Additional File 1: Supplementary Methods.
All participants were provided with Oura Rings, a well-validated wearable health tracker used to assess sleep and activity [25, 26]. The rings were worn on their non-dominant hand, and data across a four-week period (Additional File 1: Supplementary Methods) were averaged for each individual. Questionnaires assessing socio-demographic information and medical history were also obtained during study enrolment, while cardiometabolic health markers (see Cardiometabolic Measures) were taken within one month of the Oura Ring data-collection period. All studies were approved by the ethics review board of the National University of Singapore.
Assessment of 24 h movement behaviours
Key movement behaviours - physical activity (PA), sedentary behaviours (SB) and sleep, were obtained using intraday data available as 5-min metabolic equivalent (MET) epochs based on accelerometry levels from the Oura Ring following proprietary algorithms.1 MET epochs were categorized into 5 intensity levels from 4am to 3.59am the next day: 1 = sleep, 2 = SB (1-1.5 METs), 3 = light PA (1.5-3 METs), 4 = moderate PA (3–6 METs), and 5 = vigorous PA (> 6 METs). Duration spent in sleep (category 1), SB (category 2) and PA (category 3–5) was calculated by summing all 5-min epochs corresponding to each category.
Total PA (i.e., the combined duration of light (LPA) and moderate-to-vigorous activity (MVPA)) was modelled as the main exposure variable to: (1) simplify the compositional analysis while preserving interpretability of 24-hour behaviour reallocations, (2) examine the impact of overall movement given that we did not have contextual information about the types of activities participants engaged in, and (3) capture total ‘active time’ in a manner that reflects real-world behaviour patterns. Separately, we also conducted sensitivity analyses for LPA and MVPA (see Additional File 1: Supplementary Fig. 1), which showed associations with cardiometabolic markers in the same direction and supports the use of total PA as the main analytic exposure. To further visualize differences in the distribution of activity across 24 h, heatmaps indicating likelihood of daily PA (0 = no PA, 1 = PA) in 5-min bins were plotted and averaged within each group.
Although our primary analyses used 5-min MET categories to classify 24 h movement behaviours, Oura-derived sleep metrics from the main sleep period (i.e. from the longest sleep period in a day) are also presented in Additional File 1: Supplementary Table 1 to facilitate within-sleep period comparisons across age groups. These include: (1) time-in-bed (TIB): representing duration of time spent in bed, (2) total sleep time (TST): representing actual time spent asleep out of the time spent in bed, (3) wake after sleep onset (WASO): denoting time spent awake after the initial sleep onset, (4) sleep fragmentation index (SFI): which quantifies sleep disturbance as the sum of a Movement Index (percentage of movement epochs) and a Fragmentation Index (percentage of sleep epochs lasting ≤ 1 min), and (5) sleep efficiency: 100*TST/TIB.
Data filtering
Days were excluded from analysis if: (1) participants were travelling outside of Singapore, (2) 5-min daily MET epoch counts did not span the 24 h day (< 288 epochs) due to battery depletion, (3) ring non-wear was >4 h, (4) main sleep period duration (time in bed) was <3 h or ≥ 12 h which could indicate highly anomalous sleep, or (5) main sleep period bedtime occurred before 6pm or after 4am. Following day-level filtering, participants with fewer than 14 days of valid data remaining were excluded from the analysis (Fig. 1).
Fig. 1.

CONSORT diagram illustrating the flow of participants and exclusion criteria across the 3 samples studied (university students, working adults, and older adults). List of abbreviations: MET metabolic equivalent, TIB time-in-bed, BT bedtime
Cardiometabolic measures
Working and older adults underwent assessments for height, weight, and waist circumference, as well as applanation tonometry (SphygmoCor, Cardiex Ltd). Two aspects of cardiometabolic risk were examined in the current study: obesity and arterial stiffness.
To assess obesity, two widely accepted measures were computed: Body Mass Index (BMI) and Body Roundness Index (BRI). Although BMI is widely used, it may underestimate adiposity in older adults due to age-related reductions in lean and bone mass, and may overestimate adiposity in individuals with high muscle mass. BRI has thus been proposed as a more appropriate indicator of obesity [27].
To assess arterial stiffness, carotid-femoral pulse wave velocity (PWV) was determined using a SphygmoCor system (AtCor Medical/CardieX, Sydney, Australia). Additionally, two other indicators of arterial stiffness were obtained via radial artery tonometry: aortic or central pulse pressure (CPP, the difference between convolved aortic systolic and diastolic pressure) and augmentation index (AIx, reflecting the timing and quantum of wave reflection from branch points or areas of impedance mismatch which are determined by aortic stiffness and arteriolar tone). In addition to PWV, a vascular health composite score (zComposite [28]) was computed as a cardiovascular health outcome:
zComposite = average of ZPWV+ZCPP+ZAIx.
Statistical analysis
Group differences in demographic characteristics, time spent in each movement behaviour (PA, SB and sleep) and cardiometabolic outcomes were evaluated using analysis of variance (ANOVA) tests, and statistical significance was set at p < 0.05.
Compositional data analyses (CoDA) were conducted in the working-age and older adults to examine the relationship between cardiometabolic risk factors (BRI, BMI, PWV and zComposite), and the composition of PA, SB and sleep across an average day. This approach appropriately accounts for the co-dependent nature of time-use data by modelling log-ratios (log-transformed ratios between movement behaviours), thereby describing relative time spent in different behaviours rather than absolute time in any single behaviour. Specifically, we used isometric log-ratio (ilr) pivot coordinates to represent and adjust for the 24-hour movement behaviour composition [29]. In the current study, non-wear time was considered sedentary to preserve a 24-hour profile and avoid inflation of activity. Cardiometabolic outcomes were analysed in the combined working-age and older adult sample to maximise statistical power and provide more stable estimates for the compositional analyses.
Results from the compositional models are presented in three stages. First, overall CoDA regression results visualized using ternary plots, illustrate associations between cardiometabolic outcomes and the 24-hour composition of PA, SB, and sleep. Second, omnibus time substitution analyses are presented using forest plots, estimating associations when a fixed duration of time is reallocated to one behaviour proportionally from the others (e.g., 30 min/day to PA from SB and sleep). For example, reallocating 30 min/day to PA from a baseline composition of PA = 300 min, SB = 600 min, sleep = 540 min, for example, would involve proportionally reducing time from SB and sleep based on their relative contributions to the remaining 1140 min (600 + 540). In this example, approximately 16 min would be taken from SB and 14 min from sleep. Third, pairwise (isotemporal) substitution analyses were conducted for behaviour-pairs significant in the omnibus models, estimating associations when time is directly substituted from one behaviour to another (e.g., replacing SB with PA). All estimates are expressed relative to the sample’s mean 24-hour composition and represents the expected change in cardiometabolic outcomes associated with different patterns of time substitution for a hypothetical average individual. Substitution effects were obtained by using the compositional models to estimate outcome differences relative to this mean behaviour composition for specific substitutions of time (e.g. ± 30 min) between behaviours.
Age and sex were included as covariates in all CoDA models, as well as the sleep fragmentation index (SFI) to account for movement during sleep. Models were further adjusted for self-reported hypertension, diabetes, hyperlipidemia, and smoking status.
Analyses were conducted in R (version 4.4.2), with compositional data analyses performed using the epicoda package [30].
Results
Sample characteristics
After exclusion of ineligible records (see Fig. 1), the final analyses included 1,967 participants (500 university students [50.8% female], 437 working adults [61.3% female], and 1,030 older adults [53.5% female]) who contributed 48,535 valid days of movement behaviour data. Table 1 and Additional File 1: Supplementary Table 2 summarize demographic information and cardiometabolic health indicators.
Table 1.
Sample characteristics
| University Students N = 500 |
Working Adults N = 437 |
Older Adults N = 1,030 |
F/χ²/t-values | |
|---|---|---|---|---|
| Age (y) | 19.9 (1.3) | 41.1 (10.0) | 74.0 (2.6) | 20,258*** |
| Female (%) | 254 (50.8%) | 268 (61.3%) | 551 (53.5%) | 11.39** |
| Wear time (min) | 1386 (30) | 1374 (34) | 1377 (31) | 20.55*** |
| PA Duration (min) | 320.28 (86.35) | 346.55 (84.74) | 420.28 (129.27) | 160.8*** |
| MVPA Duration (min) | 45.78 (21.82) | 55.03 (29.55) | 80.26 (54.82) | 123.4*** |
| LPA Duration (min) | 274.50 (75.11) | 291.52 (71.96) | 340.02 (102.95) | 104.1*** |
| Sedentary Time (min) | 633.89 (77.34) | 581.28 (78.92) | 500.86 (108.77) | 352.8*** |
| Sleep (min) | 431.75 (48.33) | 445.77 (55.23) | 455.62 (79.01) | 21.27*** |
| BMI (kg/m2) | 21.72 (3.34) | 24.69 (4.70) | 23.99 (3.57) | 81.53*** |
| BRI | - | 3.61 (1.32) | 4.71 (1.38) | 13.25*** |
| Systolic BP (mmHg) | - | 119.29 (14.23) | 135.93 (18.30) | 17.60*** |
| Diastolic BP (mmHg) | - | 75.80 (9.90) | 76.37 (9.77) | 0.97 |
| PWV (m/s) | - | 5.63 (1.39) | 9.26 (2.07) | 35.00*** |
| CPP (mmHg) | - | 43.52 (8.04) | 53.95 (12.63) | 16.67*** |
| AIx | - | 18.36 (13.62) | 27.65 (9.24) | 12.36*** |
| Values represent mean (SD) | ||||
*** p < 0.001; p < 0.05
PA – physical activity, MVPA – moderate-to-vigorous physical activity, LPA – light physical activity, BMI – body mass index, BRI – body roundness index, PWV – pulse wave velocity, BP – blood pressure, CPP – central pulse pressure, AIx – augmentation index
Working adults and older adults in the current analyses were generally healthy, with an average BMI of 24.25 kg/m2, BRI of 4.29 and PWV of 7.86 m/s. A small but significant age-related decrease was observed for BMI, r(1120) = -0.07, p < 0.05; whereas significant age-related increases were observed for BRI, r(1110) = 0.35, p < 0.001; PWV, r(1108) = 0.71, p < 0.001; and zComposite, r(1103) = 0.63, p < 0.001, consistent with existing literature on aging and cardiovascular risk markers [31].
Age-related differences in 24 h movement behaviours
Greater PA and lower SB across the 24 h day was observed with older age (Table 1). PA was longest in the older adults (420.28 min), followed by the working adults (346.55 min) and university students (320.28 min); this trend was evident on both weekdays and weekends (Additional File 1: Supplementary Table 3) and when considering both light and moderate-to-vigorous physical activity (Table 1). Conversely, SB was the shortest in the older adults (500.86 min), followed by the working adults (581.28 min) and university students (633.89 min).
Time allocated for sleep across the 24 h day was also longest among the older adults (455.62 min vs. 445.77 min in the working adults and 431.75 min in the university students (Table 1). However, when considering main sleep metrics, actual time spent asleep was shortest in older adults (Additional File 1: Supplementary Table 1) due to more fragmented sleep - resulting in overall higher sleep fragmentation (SFI) scores, increased wake after sleep onset (WASO), and reduced sleep efficiency (Additional File 1: Supplementary Table 1).
Heatmaps (Fig. 2) indicate that older adults were active throughout the day, except for a dip during the afternoon. In contrast, both students and working adults had lower likelihood of weekday PA, with activity concentrated at specific times. In students, weekday PA was most likely to occur around the start and end of lessons, reflecting movement from class to class. Working adults demonstrated higher PA likelihood during commute hours in the mornings and evenings, as well as around lunchtime.
Fig. 2.

Heatmaps depicting likelihood of PA across three groups of adults (university students, working adults, older adults). Each row of a heatmap represents a 24 h day, while each heatmap has 21 rows (days) starting from the first Monday recorded for each participant’s four-week collection period. Each cell of a row corresponds to a 5-min epoch across the 24 h day. Heatmaps were averaged across participants within each group. Colours in each cell represent the likelihood of PA occurrence in that age group (cool – low, hot – high). Among the three age groups, older adults had a higher likelihood of PA throughout the daytime, while students and working adults tended to have greater PA around class/work hours on weekdays. Note: Day 5 in the student group (top panel) was a public holiday, hence its activity distribution was more similar to a weekend (Days 6–7) than a weekday (Days 1–4)
On the weekends, PA likelihood was markedly lower and started later in university students compared to weekdays. Although PA likelihood in working adults appeared to be preserved on weekends, its start time was delayed and more evenly spread out over the day. These observations lie in contrast to older adults in whom the likelihood and timing of PA was similar across weekdays and weekends.
Impact of time reallocation between movement behaviours on cardiometabolic measures by CoDA
Overall CoDA regressions show that increasing PA, by taking time from other behaviours, is associated with lower BMI (beta=-1.16, 95% CI=-1.89 to -0.73), BRI (beta=-0.35, 95% CI=-0.6 to -0.1), PWV (beta=-0.57, 95% CI=-0.89 to -0.24) and zComposite (beta=-0.12, 95% CI=-0.22 to -0.02) (ternary plots; Figs. 3 and 4).
Fig. 3.

Compositional regression analyses showing that reallocating time to more physical activity (PA) was associated with lower BMI and body roundness index (BRI). Each dot in the ternary plots represents the 24 h activity composition of one participant, with the solid black triangle indicating the sample mean composition. The distribution of dots is identical across all ternary plots. Dot colours are weighted by the regression beta estimates, illustrating that participants with higher PA had lower BMI and BRI (blue shading toward the more active corner). The accompanying forest plots display substitution model results, demonstrating that reallocating 30 min of sedentary time to PA or sleep was associated with lower BMI and BRI.
Fig. 4.

Compositional regression analyses showing that reallocating time to more physical activity (PA) was associated with lower cardiometabolic risk. Each dot in the ternary plots represents the 24 h activity composition of a single participant, with the solid black triangle indicating the sample mean composition. The distribution of dots is identical across all ternary plots. Dot colours are weighted by the regression beta estimates, illustrating that participants with higher PA had lower PWV and zComposite (blue shading toward the more active corner). The accompanying forest plots display substitution model results, demonstrating that reallocating 30 min more PA was associated with lower PWV and zComposite.
To facilitate interpretation of these effect sizes, omnibus substitution analyses (forest plots; Figs. 3 and 4) show that adding 30 min of PA proportionally from other behaviours was related to decreases in BMI (-0.13 kg/m2), BRI (-0.04), PWV (-0.05 m/s) and zComposite (-0.01). Similarly, adding 30 min of sleep from other behaviours was associated with lower BMI (-0.21 kg/m2) and BRI (-0.05), while reducing 30 min of SB related to lower BMI (-0.28 kg/m2) and BRI (-0.07).
Isotemporal (pairwise) substitution analyses between PA and SB further show that increasing PA time by taking time from SB related to lower BMI, BRI, PWV and zComposite (Additional File 1: Supplementary Fig. 2). Increasing sleep, also by taking time from SB, was related to lower BMI and BRI (Additional File 1: Supplementary Fig. 3). Time reallocations between PA and sleep were not significantly associated with cardiometabolic outcomes.
Discussion
Using objective wearable data across three adult cohorts in Singapore, we showed that contemporary patterns of physical activity and sedentary behaviour no longer conform to long-standing epidemiological assumptions in which older adults are the least active and working-age or older adults the most sedentary [5–8]. Notably, we observed that university students in our sample averaged only 320.28 min of daily physical activity compared to 420.28 min in the older adults, and they also spent 633.89 min being sedentary, compared to 500.86 min in the older adults.
While lower PA levels in students can be expected on weekdays due to classes and other academic commitments, PA declined by a further ~ 30-min on the weekends – which could suggest that opportunities to increase PA were not taken. While sedentary time also decreased on the weekends, this reduction was offset by increased sleep time, consistent with weekend “catch-up” sleep [32]. Among working-age adults however, PA duration was largely preserved on the weekends. The onset of PA shifted later and was distributed more evenly across the day. Reductions in sedentary time during the weekends were also primarily replaced by longer sleep. Remarkably, older adults exhibited the highest total PA on both weekdays and weekends, averaging ~ 60–100 min more per day than the students and working-age adults. Time spent sedentary was also the lowest; averaging ~ 15–140 min less per day. Older adults allocated the longest time for sleep (time in bed) on average, but actual total sleep time was the shortest - consistent with established age-related declines in sleep efficiency and increased sleep fragmentation [33]. They also showed the greatest stability in PA, SB, and sleep across the week. Taken together, these findings indicate that older adults’ movement behaviours reached favourable levels and were well distributed temporally across the week, despite their shorter and more fragmented sleep. Conversely, students, despite a greater capacity to be more physically active, did not appear to fully capitalise on this even on weekends with fewer competing commitments.
In the working-age and older adult groups, unfavourable movement profiles were associated with adverse cardiometabolic profiles. The use of compositional methods which integrate physical activity, sedentary time, and sleep as co-dependent components of a finite 24 h day allowed us to quantify how trade-offs between movement behaviours relate to cardiometabolic health [29]. In the omnibus analyses, reallocating 30 min/day toward physical activity from the remaining movement behaviours was associated with lower adiposity (BMI and BRI) as well as more favourable vascular health indicators (PWV and zComposite). In contrast, reallocating time toward sleep was associated primarily with lower adiposity, while reducing sedentary behaviour was similarly linked to lower adiposity and improved overall vascular health. Pairwise substitution analyses further indicated that these associations were largely driven by the exchange of sedentary behaviour with either physical activity or sleep. Specifically, replacing sedentary time with physical activity was associated with favourable differences across both adiposity and vascular outcomes, whereas replacing sedentary time with sleep was associated with lower adiposity alone.
Collectively, these findings suggest that greater physical activity is associated with the broadest cardiometabolic benefits, while associations with longer sleep are largely confined to adiposity-related measures. The absence of significant associations when time was exchanged between physical activity and sleep further suggests that both behaviours may be beneficial relative to sedentary behaviour, rather than one being consistently superior to the other. Consequently, reducing sedentary time—whether through greater physical activity or longer sleep duration—may be more important than shifting time between physical activity and sleep itself. These findings also align with prior studies [34–36] reporting cardiometabolic benefits when sedentary time is substituted with PA or sleep (particularly for short sleepers [37]) - with improvements observed across adiposity, lipid profiles, and glycemic indices.
Our findings of greater inactivity among university students contrast with earlier Singaporean surveys [38], past actigraphic studies [39], and Western data showing age-related declines in physical activity [40]. While underlying drivers of increased sedentary behaviours and decreased physical activity were not directly assessed, they likely reflect broader societal shifts associated with pervasive digitalisation of education, work, transport, and leisure. These habits – particularly pronounced amongst the young who have grown up with this way of life, have been facilitated by the widespread availability and affordability of portable electronic devices, streaming media, online education, food delivery, and ride-hailing services, all of which have collectively reduced the need even for incidental movement [41, 42]. Although cardiometabolic outcomes were not assessed in the university student cohort, their relatively low physical activity and high sedentary time may represent an unfavourable movement behaviour profile that warrants prospective follow-up to determine whether it translates into increased cardiometabolic risk later in adulthood. Globally, physical inactivity is already estimated to cost health care systems USD 53.8 billion annually, while in Singapore, the economic cost of physical inactivity is estimated to be USD 201 million [43, 44]. Modelling studies further suggest that a 10y population-wide physical activity programme in Singapore could lead to a reduction in health care costs of SGD (Singapore dollar) 448 million through the prevention of diabetes, hypertension, and related complications [43], underscoring the substantial health and economic benefits of scalable, population-level interventions that increase physical activity and reduce sedentary behaviour. Preventive strategies must therefore happen now, not only by encouraging promotion of weekday bouts of activity but also by considering how urban environments and digital environments can be redesigned to restore incidental and habitual movement in younger generations.
This study has several notable strengths, including the use of objective, high-resolution wearable data collected under free-living conditions and harmonised across three cohorts spanning early adulthood to older age. The integration of physical activity, sedentary behaviour, and sleep within a 24-h compositional framework further allowed us to examine realistic behavioural trade-offs as they occur in daily life. Against this backdrop, several limitations warrant consideration. First, the findings are derived from convenience samples of individuals who volunteered for a consumer-technology tracking study. Although devices were provided to ensure that this would not be a barrier to participation, such individuals may not be representative of the general population. Second, confounding by sociodemographic factors apart from age cannot be fully excluded. The older adult cohort was restricted to ethnic Chinese participants by design, although this also comprised the majority ethnic group in the other two cohorts. However, in a separate sensitivity analysis limited to only participants of Chinese ethnicity with equal male-female representation across all cohorts, we observed the same age-related gradients in movement behaviour profiles as in the full cohort, suggesting that the findings were not driven by differences in ethnicity or sex composition (Additional File: Supplementary Table 4). Nonetheless, we could not completely account for socioeconomic status through housing information, as over half of the university students resided on campus. Third, although 5-minute MET intervals were used here, the optimal time scale for capturing health-relevant movement patterns remains uncertain, given the limited experimental evidence comparing short and long activity bouts. Finally, substitution estimates should be interpreted as hypothetical associations. Further experimental and intervention studies are needed to determine the feasibility and real-world implications of these reallocations and to assess whether the estimated changes in behaviour translate into meaningful health benefits.
Conclusions
Using a compositional framework, we found that university students accumulated less physical activity and more sedentary behaviour than both working-age and older adults, highlighting young adulthood as a potentially important target for movement behaviour interventions. Furthermore, in the working-age and older adults who had cardiometabolic assessments, reallocating time away from sedentary behaviour was associated with more favourable adiposity and vascular health profiles. Together, these findings underscore the importance of considering the entire 24-hour movement behaviour composition, rather than individual behaviours in isolation, when evaluating cardiometabolic health and informing public health strategies.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
The authors would like to thank Nicholas Chee, Kian Foong Wong, Liang Tian, Yashmit Lepcha, Kyra Chong, Shohreh Ghorbani, Zhenghao Pu, Alexander Soo, Annalissa Munoz, Nicha Turton and the SG70 team for their contributions to data collection; and Aren Ung for generating the heat-map plots.
Abbreviations
- AIx
augmentation index
- ANOVA
analysis of variance
- BMI
body mass index
- BP
blood pressure
- BRI
body roundness index
- CoDA
compositional data analyses
- CPP
central pulse pressure
- LPA
light physical activity
- MET
metabolic equivalent
- MVPA
moderate-to-vigorous physical activity
- PA
physical activity
- PWV
pulse wave velocity
- SB
sedentary behaviour
- SD
standard deviation
- SGD
Singapore dollar
- USD
US dollar
Author contributions
JLO, SQ and MWLC designed the study, generated hypotheses and drafted the manuscript. XYC and CSS oversaw the data collection and curation of the wearable data streams. JLO, SQ and THM analysed and interpreted the data. GY, LHL, FMR and WPK critically reviewed the manuscript and contributed to the discussion of the findings. All authors read and approved the final manuscript.
Funding
The study was supported by Centre Funding for the Centre for Sleep and Cognition, National University of Singapore, and the Lee Foundation.
Data availability
The data in this article are available upon reasonable request with a signed data access agreement. For further information, please contact the corresponding author.
Declarations
Ethics approval and consent to participate
All three study protocols were approved by the ethics review board of the National University of Singapore (university students: NUS-IRB-2023-110, working adults: NUS-IRB-2024-486, older adults: NUS-IRB-2020-398). All participants signed informed consent before study participation in accordance with the Declaration of Helsinki. Two studies were registered on ClinicalTrials.gov (university students: NCT05977517 [registered: 26 July 2023], working adults: NCT06594549 [registered: 3 September 2024]).
Consent for publication
Not applicable.
Competing interests
Michael W. L. Chee is a member of the medical advisory board of Ouraring Inc. As of August 2026, J.L.O, S.Q. and X.Y.C are members of the Oura–National University of Singapore (NUS) Joint Lab. This work was however conducted independently of the Joint Lab and was designed, funded, and executed solely by NUS. No other disclosures were reported.
Footnotes
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Ju Lynn Ong and Shuo Qin contributed equally to this work.
References
- 1.Lee I-M, Shiroma EJ, Lobelo F, Puska P, Blair SN, Katzmarzyk PT. Effect of physical inactivity on major non-communicable diseases worldwide: an analysis of burden of disease and life expectancy. Lancet. 2012;380(9838):219–29. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Biswas A, Oh PI, Faulkner GE, Bajaj RR, Silver MA, Mitchell MS, et al. Sedentary time and its association with risk for disease incidence, mortality, and hospitalization in adults: a systematic review and meta-analysis. Ann Intern Med. 2015;162(2):123–32. [DOI] [PubMed] [Google Scholar]
- 3.Ajufo E, Kany S, Ramo JT, Churchill TW, Guseh JS, Aragam KG, et al. Accelerometer-Measured Sedentary Behavior and Risk of Future Cardiovascular Disease. J Am Coll Cardiol. 2025;85(5):473–86. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Panahi S, Tremblay A. Sedentariness and Health: Is Sedentary Behavior More Than Just Physical Inactivity? Front Public Health. 2018;6:258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Troiano RP, Berrigan D, Dodd KW, Masse LC, Tilert T, McDowell M. Physical activity in the United States measured by accelerometer. Med Sci Sports Exerc. 2008;40(1):181–8. [DOI] [PubMed] [Google Scholar]
- 6.Hallal PC, Andersen LB, Bull FC, Guthold R, Haskell W, Ekelund U, et al. Global physical activity levels: surveillance progress, pitfalls, and prospects. Lancet. 2012;380(9838):247–57. [DOI] [PubMed] [Google Scholar]
- 7.Nagata JM, Vittinghoff E, Gabriel KP, Rana JS, Garber AK, Moran AE, et al. Physical activity from young adulthood to middle age and premature cardiovascular disease events: a 30-year population-based cohort study. Int J Behav Nutr Phys Act. 2022;19(1):123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Matthews CE, Chen KY, Freedson PS, Buchowski MS, Beech BM, Pate RR, et al. Amount of time spent in sedentary behaviors in the United States, 2003–2004. Am J Epidemiol. 2008;167(7):875–81. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Patel SR, Malhotra A, White DP, Gottlieb DJ, Hu FB. Association between reduced sleep and weight gain in women. Am J Epidemiol. 2006;164(10):947–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Cappuccio FP, Taggart FM, Kandala NB, Currie A, Peile E, Stranges S, et al. Meta-analysis of short sleep duration and obesity in children and adults. Sleep. 2008;31(5):619–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Chaput JP, Despres JP, Bouchard C, Tremblay A. The association between sleep duration and weight gain in adults: a 6-year prospective study from the Quebec Family Study. Sleep. 2008;31(4):517–23. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Robertson MD, Russell-Jones D, Umpleby AM, Dijk DJ. Effects of three weeks of mild sleep restriction implemented in the home environment on multiple metabolic and endocrine markers in healthy young men. Metabolism. 2013;62(2):204–11. [DOI] [PubMed] [Google Scholar]
- 13.Rafalson L, Donahue RP, Stranges S, Lamonte MJ, Dmochowski J, Dorn J, et al. Short sleep duration is associated with the development of impaired fasting glucose: the Western New York Health Study. Ann Epidemiol. 2010;20(12):883–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Robillard R, Lanfranchi PA, Prince F, Filipini D, Carrier J. Sleep deprivation increases blood pressure in healthy normotensive elderly and attenuates the blood pressure response to orthostatic challenge. Sleep. 2011;34(3):335–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.St-Onge MP, Grandner MA, Brown D, Conroy MB, Jean-Louis G, Coons M, et al. Sleep Duration and Quality: Impact on Lifestyle Behaviors and Cardiometabolic Health: A Scientific Statement From the American Heart Association. Circulation. 2016;134(18):e367–86. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Lloyd-Jones DM, Allen NB, Anderson CAM, Black T, Brewer LC, Foraker RE, et al. Life’s Essential 8: Updating and Enhancing the American Heart Association’s Construct of Cardiovascular Health: A Presidential Advisory From the American Heart Association. Circulation. 2022;146(5):e18–43. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.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. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Chastin SF, Palarea-Albaladejo J, Dontje ML, Skelton DA. Combined Effects of Time Spent in Physical Activity, Sedentary Behaviors and Sleep on Obesity and Cardio-Metabolic Health Markers: A Novel Compositional Data Analysis Approach. PLoS ONE. 2015;10(10):e0139984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Janssen I, Clarke AE, Carson V, Chaput JP, Giangregorio LM, Kho ME, et al. A systematic review of compositional data analysis studies examining associations between sleep, sedentary behaviour, and physical activity with health outcomes in adults. Appl Physiol Nutr Metab. 2020;45(10):S248–57. (Suppl. 2)). [DOI] [PubMed] [Google Scholar]
- 20.Pfledderer CD, Mullane EJ, Brown DMY, Burkart S, Hunt ET, Johnson A, et al. Five-year trends in U. S. child and adolescent 24-hour movement behavior guideline adherence, 2018–2022. J Act Sedentary Sleep Behav. 2025;4(1):16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Husu P, Tokola K, Vaha-Ypya H, Sievanen H, Kokko S, Villberg J, et al. Physical activity has decreased in Finnish children and adolescents from 2016 to 2022. BMC Public Health. 2024;24(1):1343. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Safar ME, Czernichow S, Blacher J. Obesity, arterial stiffness, and cardiovascular risk. J Am Soc Nephrol. 2006;17(4 Suppl 2):S109–11. [DOI] [PubMed] [Google Scholar]
- 23.Soon CS, Chua XY, Leong RLF, Ong JL, Massar SAA, Qin S, et al. A longitudinal study of sleep in university freshmen: facilitating and impeding factors. Sleep. 2025;48(10):zsaf156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Qin S, Ng EKK, Soon CS, Chua XY, Zhou JH, Koh WP, et al. Association between objectively measured, multidimensional sleep health and cognitive function in older adults: cross-sectional wearable tracker study. Sleep Med. 2025;132:106569. [DOI] [PubMed] [Google Scholar]
- 25.Ong JL, Golkashani HA, Ghorbani S, Wong KF, Chee N, Willoughby AR, et al. Selecting a sleep tracker from EEG-based, iteratively improved, low-cost multisensor, and actigraphy-only devices. Sleep Health. 2024;10(1):9–23. [DOI] [PubMed] [Google Scholar]
- 26.Kristiansson E, Fridolfsson J, Arvidsson D, Holmang A, Borjesson M, Andersson-Hall U. Validation of Oura ring energy expenditure and steps in laboratory and free-living. BMC Med Res Methodol. 2023;23(1):50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Thomas DM, Bredlau C, Bosy-Westphal A, Mueller M, Shen W, Gallagher D, et al. Relationships between body roundness with body fat and visceral adipose tissue emerging from a new geometrical model. Obes (Silver Spring). 2013;21(11):2264–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Lim SL, Gao Q, Nyunt MS, Gong L, Lunaria JB, Lim ML, et al. Vascular Health Indices and Cognitive Domain Function: Singapore Longitudinal Ageing Studies. J Alzheimers Dis. 2016;50(1):27–40. [DOI] [PubMed] [Google Scholar]
- 29.Dumuid D, Stanford TE, Martin-Fernandez JA, Pedisic Z, Maher CA, Lewis LK, et al. Compositional data analysis for physical activity, sedentary time and sleep research. Stat Methods Med Res. 2018;27(12):3726–38. [DOI] [PubMed] [Google Scholar]
- 30.Walmsley R, Chan S, Smith-Byrne K, Ramakrishnan R, Woodward M, Rahimi K, et al. Reallocation of time between device-measured movement behaviours and risk of incident cardiovascular disease. Br J Sports Med. 2021;56(18):1008–17. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Zhao D, Wang Y, Wong ND, Wang J. Impact of Aging on Cardiovascular Diseases: From Chronological Observation to Biological Insights: JACC Family Series. JACC Asia. 2024;4(5):345–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Hershner SD, Chervin RD. Causes and consequences of sleepiness among college students. Nat Sci Sleep. 2014;6:73–84. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Evans MA, Buysse DJ, Marsland AL, Wright AGC, Foust J, Carroll LW, et al. Meta-analysis of age and actigraphy-assessed sleep characteristics across the lifespan. Sleep. 2021;44(9):zsab088. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Collings PJ, Backes A, Aguayo GA, Fagherazzi G, Malisoux L, group O-Ls. Substituting device-measured sedentary time with alternative 24-hour movement behaviours: compositional associations with adiposity and cardiometabolic risk in the ORISCAV-LUX 2 study. Diabetol Metab Syndr. 2023;15(1):70. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Farrahi V, Rostami M, Nauha L, Korpisaari M, Niemela M, Jamsa T, et al. Replacing sedentary time with physical activity and sleep: Associations with cardiometabolic health markers in adults. Scand J Med Sci Sports. 2023;33(6):907–20. [DOI] [PubMed] [Google Scholar]
- 36.Van Der Sluijs KM, Vloet JIA, Thijssen DHJ, Eijsvogels TMH, Bakker EA, Nijmegen Exercise Study C. Cardiometabolic Benefit of Replacing Sedentary Time with Light-Intensity Physical Activity: Compositional Data Analysis of the Nijmegen Exercise Study. Med Sci Sports Exerc. 2025;57(8):1711–20. [DOI] [PubMed] [Google Scholar]
- 37.Collings PJ, Backes A, Malisoux L. group O-Ls. Arterial stiffness and the reallocation of time between device-measured 24-hour movement behaviours: A compositional data analysis. Atherosclerosis. 2023;379:117185. [DOI] [PubMed] [Google Scholar]
- 38.Lau JH, Nair A, Abdin E, Kumarasan R, Wang P, Devi F, et al. Prevalence and patterns of physical activity, sedentary behaviour, and their association with health-related quality of life within a multi-ethnic Asian population. BMC Public Health. 2021;21(1):1939. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Muller AM, Tan CS, Chu AHY, van Dam RM, Mueller-Riemenschneider F. Associations between psychological factors and accelerometer-measured physical activity in urban Asian adults. Int J Public Health. 2019;64(5):659–68. [DOI] [PubMed] [Google Scholar]
- 40.Strain T, Flaxman S, Guthold R, Semenova E, Cowan M, Riley LM, et al. National, regional, and global trends in insufficient physical activity among adults from 2000 to 2022: a pooled analysis of 507 population-based surveys with 5.7 million participants. Lancet Glob Health. 2024;12(8):e1232–43. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Ng SW, Popkin BM. Time use and physical activity: a shift away from movement across the globe. Obes Rev. 2012;13(8):659–80. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Chen M, Padmapriya N, Chua XH, Escobosa LLT, Tay AE, Tai BC, et al. Screen viewing patterns and their association with mental wellbeing and psychological distress: a cross-sectional study amongst university students. BMC Public Health. 2024;24(1):2097. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Ang G, Tan CS, Teerawattananon Y, Muller-Riemenschneider F, Chen C. A Nationwide Physical Activity Intervention for 654,500 Adults in Singapore: Cost-Utility Analysis. JMIR Public Health Surveill. 2024;10:e46178. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Ding D, Lawson KD, Kolbe-Alexander TL, Finkelstein EA, Katzmarzyk PT, van Mechelen W, et al. The economic burden of physical inactivity: a global analysis of major non-communicable diseases. Lancet. 2016;388(10051):1311–24. [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 data in this article are available upon reasonable request with a signed data access agreement. For further information, please contact the corresponding author.
