Skip to main content
The International Journal of Behavioral Nutrition and Physical Activity logoLink to The International Journal of Behavioral Nutrition and Physical Activity
. 2026 Jun 23;23:84. doi: 10.1186/s12966-026-01939-4

Mobility measures and waking-day movement behaviour composition among older adults: a compositional data analysis of the McMaster Monitoring My Mobility study

Shawn Hakimi 1, Renata Kirkwood 1, Stuart M Phillips 2, Rong Zheng 3, Marla K Beauchamp 1,✉
PMCID: PMC13548552  PMID: 42337742

Abstract

Background

Mobility is a cornerstone of healthy ageing typically assessed using self-report and performance-based measures. Recent research suggests these measures are poor proxies for real-world mobility. Device-derived measures of real-world mobility reflect the relative proportions of time a person allocates to sedentary behaviour (SB), light-intensity physical activity (LIPA), and moderate-to-vigorous physical activity (MVPA) that together form the waking-day movement behaviour composition. The aim of this study was to examine the associations between commonly used mobility measures and the waking-day movement behaviour composition in older adults.

Methods

A cross-sectional analysis of data from over 1200 older adults ≥ 65 years of age from the baseline cohort (2022–2024) of the McMaster Monitoring My Mobility (MacM3) study was conducted. Compositional data analysis was used to examine the associations between 6 self-report and 10 performance-based measures of mobility and multiple components of the waking-day movement behaviour composition and establish differences in movement behaviours according to different levels of mobility. Examples of included measures are the Physical Activity Scale for the Elderly (PASE) and Timed Up and Go (TUG).

Results

Data from 1227 older adults (73.6 ± 5.3 years) were analysed. Significant differences in waking-day movement behaviour composition were found across the self-report and performance-based mobility measures. Older adults with lower mobility accumulated more SB and less MVPA throughout the day. For example, those with poorer TUG performance accumulated 34 more minutes/day of SB, and 22 min/day less of MVPA compared to those with better performance. The PASE, 400-meter walk, and fast gait speed tests were the strongest indicators of real-world mobility; however, the effect sizes were small. No measure showed a significant association with LIPA.

Conclusions

Traditional self-report and performance-based measures of mobility are associated with the waking-day movement behaviour composition in older adults; however, their ability to explain real-world mobility is limited and varies across measures. The lack of association between any of the measures and LIPA is surprising, given that older adults spend most of their time in this activity intensity. These findings challenge the widespread use of traditional mobility measures to make inferences about real-world mobility.

Supplementary Information

The online version contains supplementary material available at https://doi.org/10.1186/s12966-026-01939-4.

Keywords: Physical activity, Sedentary behaviour, Time-use epidemiology, Ageing, Physical functioning, Quality of life, Locomotor, Ambulation, Geriatric

Background

Mobility is a cornerstone of healthy ageing regarded by ageing experts as the ‘6th vital sign’ [1]. Mobility limitations such as difficulty walking, bending, or climbing several flights of stairs are a strong predictor of falls, hospitalisation, institutionalisation and death in older people [2]. Although mobility has been defined in various ways [3], the World Health Organization (WHO) more recently defines it as “movement in all its forms whether powered by the body (with or without an assistive device) or a vehicle” [4], building on its earlier definition within the International Classification of Functioning, Disability and Health (ICF) framework as “changing body position or location or by transferring from one place to another, by carrying, moving or manipulating objects, by walking, running, or climbing, and by using various forms of transportation” [5]. Together, these definitions reflect a multidimensional construct, which underscores the need for comprehensive approaches for measuring mobility in older adults [6].

In practice, mobility is often assessed using a range of self-report and performance-based measures [6–8]. Self-report measures typically capture perceived ability (e.g., Late Life Function and Disability Instrument [LLFDI]) and/or frequency and extent of movement across environments (e.g., Life Space Assessment [LSA]), while performance-based measures assess physical capacity for mobility (e.g., Timed Up and Go [TUG]). Although these measures reflect different dimensions of mobility, they are frequently used (sometimes interchangeably) as proxies for overall mobility in clinical and research settings. However, the extent to which these measures reflect real-world, everyday mobility remains unclear [9, 10]. Several studies suggest they may be poor proxies, as they are prone to measurement error, conducted under standardised conditions, initiated by external cues, and may not reflect purposeful, real-world behaviour [11–13].

Real-world mobility, typically measured using wearable devices, reflects the observable expression of mobility in daily life, that is, what an individual actually does in free-living conditions. Within a multidimensional framework, this represents the enacted domain of mobility and is shaped by interactions between physiological, intrinsic, and environmental factors [14, 15]. It is operationalised as the distribution of time across movement behaviours: sedentary behaviour (SB), light-intensity physical activity (LIPA), and moderate-to-vigorous physical activity (MVPA) which together comprise the waking-day movement behaviour composition. Accordingly, it remains unclear whether commonly used self-report and performance-based measures of mobility, which primarily capture perceived ability or physical capacity, adequately reflect this real-world expression of mobility.

Historically, research on movement behaviours in older adults has focussed on physical activity, namely LIPA and MVPA [16, 17]; however, the time older adults spend in these behaviours only account for small portions of the day, 18% and 3% respectively [18–21]. Researchers now appreciate the relevance of the movement intensities that make up the remainder of the day including SB (e.g., screen time) [22]. Recent research demonstrates that the entire daily movement behaviour composition has implications for health [22, 23]. Several studies have noted that physical activity and SB can be impacted by physical functioning, gait, and balance [24–29]. While studies have examined associations between mobility measures and physical activity and SB on their own, research has not yet addressed the extent of these associations in relation to all components of the daily movement behaviour composition.

Statistical approaches that assess the association between mobility and movement behaviours should account for their compositional properties [30, 31]. Traditional statistical approaches analyse movement behaviours independently which is problematic and may lead to distorted results because movement behaviours are co-dependent whereby their summed time always equates to a fixed amount of time (e.g., waking-day hours) [30–33]. That is, if time in one movement behaviour changes, an equal and opposite change must occur in another or combination of remaining movement behaviours [30–33]. Compositional data analysis (CoDA) statistical techniques are appropriate for analysing data that is a composition of a finite whole, such as movement behaviours in the waking-day [33].

An integrated approach to understanding the associations between mobility measures and movement behaviour has implications for informing healthy ageing initiatives and identifying modifiable aspects of mobility that beneficially influence how individuals distribute time across daily movement behaviours. The objectives of this study are to use a CoDA framework to: (1) examine the extent to which commonly used self-report and performance-based measures of mobility are associated with multiple components of the waking-day movement behaviour composition and, (2) understand how older adults with different levels of mobility allocate their time in waking-day movement behaviours.

Methods

Study design and participants

This study is a cross-sectional analysis of baseline data from the McMaster Monitoring My Mobility (MacM3) study, an ongoing prospective cohort study tracking later life mobility trajectories using wearable technology [34]. The study includes 1,506 older adults from Southern Ontario, Canada. Baseline data were collected from May 2022 to June 2024. Inclusion criteria were ≥ 65 years of age, community-dwelling, provision of informed consent, absence of visual or hearing impairments that would make participation unsafe, ability to speak and understand English, and being free from major mobility limitation at baseline as determined by the Preclinical Mobility Limitation scale (PCML) [35]. Ethics approval was obtained from the Hamilton Integrated Research Ethics Board at McMaster University. Participants were largely recruited from the community through word of mouth, newspapers, and Facebook ads; a small contingent came from a pre-recruited sample from a larger intergenerational study on ageing [36].

Mobility measures

The explanatory variables are measures of mobility obtained by trained research staff: (i) self-report measures—via standardised questionnaires administered through phone-call assessments or in-person interviews; (ii) performance-based measures—a battery of physical tests collected in-person at one of two data collection sites. A detailed description of the MacM3 protocol has been published elsewhere [37].

Table 1 summarises the mobility measures, briefly describes them (refer to the reference provided for detailed information), and lists the data source. To facilitate comparison among ‘low’, ‘moderate’ and ‘high’ levels of mobility, scores for each mobility measure were grouped into tertiles [38]. In addition to examining the individual mobility measures, indices were created for each category of measure. To do that, percentile ranks of each of the individual measures were created and averaged; then, tertiles were created based on these averages. Boundary values for each tertile for all mobility measures and indices are provided in Supplementary Table A1.

Table 1.

Overview of mobility measures

Name of measure Explanation of measure and reference for measurement protocol Exposure
groups
Data
source
Self-report measures
Preclinical Mobility Limitation Scale Self-reported assessment of three preclinical mobility limitations (walking 0.5 km, walking 2 km, climbing up stairs)a Predefined groups Questionnaire
Late-Life Function and Disability Instrument-Disability Component Self-reported frequency of performing 16 life tasks and the person’s limitation in their capacity to perform those tasksb,c Tertiles Questionnaire
Late-Life Function and Disability Instrument-Physical Function Component 48 items that assess self-reported difficulty in performing discrete activities via three domains: advanced lower extremity functioning, basic lower extremity functioning and upper extremity functioningb,c Tertiles Questionnaire
Physical Activity Scale for the Elderly 12-item questionnaire that measures amount of physical activity undertaken in a 1-week periodd Tertiles Questionnaire
Life Space Assessment Life-space mobility (i.e., mobility in the home and community) measured in three sections: life-space level, frequency, independencee Tertiles Questionnaire
Mobility Assessment Tool-Short Form Animated video clips showing both the nature and demands of various tasks (e.g., climbing stairs); participant rates their ability to do that taskf Tertiles Computer-based assessment
Performance-based measures
Timed Up and Go (usual pace) Get up from chair, walk 3-meters, turn around, walk back and return to seated chair position at usual walking speedg Tertiles Physical assessment
Timed Up and Go (fast pace) Same test described above but at fast walking speedg Tertiles Physical assessment
Timed Up and Go (cognitive) Same test as described initially while performing a cognitive task (e.g., counting backwards by two from random number between 50–90)g Tertiles Physical assessment
Sit to-Stand Test Stand up 5-times from chair; starting in seated position with back straight, feet on the floor and arms crossed against chest, finished at full-hip extensionh Tertiles Physical assessment
Gait speed (usual pace) Walking 3-meters at usual pacei Tertiles Physical assessment
Gait speed (fast pace) Walking 3-meters as fast as possiblej Tertiles Physical assessment
400-meter walk Walk 400-meters as fast as possible (terminated if > 15 min)k Tertiles Physical assessment
Single-Leg Stance Hands on hips, lift one foot off the floor, and hold the position for as long as possible up to a maximum of 60 s for each legl Tertiles Physical assessment
Stair-Climbing Power Ascend a flight of four stairs with handrails (if needed) as fast as possiblem Tertiles Physical assessment

References—aManty et al. (2007) [35]; bHaley et al. (2002) [39]; cJette et al. (2002) [40]; dWashburn et al. (1993) [41]; eBaker et al. (2003) [42]; fRejeski et al. (2015) [43]; gBarry et al. (2014) [44]; hJones et al. (1999) [45]; i Abellan Van Kan et al. (2009) [46]; jBohannon, R.W. (1997) [47]; kGeorgiopoulou et al. (2017) [48]; lSpringer et al. (2007) [49]; mBean et al. (2007) [50]

Movement behaviour variables

The outcome variables were the relative proportions of the waking-day comprised of SB, LIPA, and MVPA measured via a wrist-worn smartwatch. The waking-day was defined as the period from the participant waking up until going to sleep. Participants were instructed to remove the watch and charge it at bedtime, at which point all sensors were inactive until the watch was taken off the charger and worn again the following morning.

Participants received the device at the baseline in-person assessment along with detailed instructions on proper device placement, wear time, and handling by trained research staff and were given a printed flyer containing detailed instructions and troubleshooting guidance. After the assessment period, participants mailed the device back using a prepaid postage box. Participants were asked to wear the device on their non-dominant wrist during waking hours for 10 consecutive days for at least 10 h per day except during swimming, bathing or showering. If they were unable to wear it on their non-dominant wrist, the reason (e.g., physical limitation) was recorded.

The MacM3 study uses a custom data collection application with the TicWatch Pro 3 Ultra GPS (Mobvoi, Nanjing, China) validated for capturing raw accelerometry data in older adults [34]. Raw data was processed using the NiMBaLWear analytic pipeline, a validated open-source data analytic pipeline that quantifies activity intensity from raw free-living data collected over multiple days [51]. Data was captured at 50 Hz and presented in gravitational units that was further processed using the NiMBaLWear Pipeline and the Average Vector Magnitude (AVM) of acceleration using 15-second epochs (and a normal filter) to produce counts [51]. Epochs that did not overlap with detected non-wear time were categorised as SB, LIPA, or MVPA by comparing the AVM to epoch length-independent activity intensity cut-points for older adults ≥ 60 years of age [52]. Specifically, thresholds of 42.5 mg (non-dominant wrist) and 62.5 mg (dominant wrist) were used for light activity, while 98.0 mg (non-dominant) and 92.5 mg (dominant) defined moderate activity. These cut-points have been applied in other ageing cohorts and support comparability across studies examining accelerometry-derived activity patterns [52]. Cut points were applied based on the actual wear location (non-dominant wrist or dominant), and passed to NiMBaLWear, which automatically selects the appropriate thresholds. Sleep detection was not performed; therefore, periods of daytime sleep (e.g., napping) may have been classified as SB.

Non-wear time was identified using a modified Van Hees algorithm, based on sustained periods of low acceleration over overlapping 60-minute windows [53]. Windows were advanced in 1-minute increments to improve detection resolution, and additional criteria were applied to account for short, spurious periods of movement within prolonged non-wear intervals, thereby reducing misclassification due to incidental device movement.

Participants with an average wear time of ≥ 10 h with ≥ 4 valid days of accelerometer data were included in the final study sample [54]. Movement behaviour values were calculated as proportions of each participant’s total wear time [33].

Covariates

Covariates were considered based on their known relationship with mobility measures and one or more movement behaviours. All variables were gathered at baseline through phone call assessment by trained research staff. Age (date of birth; years); sex at birth (male/female); body mass index calculated from weight (kg) and height (cm) (BMI; kg/m2); education level (no post secondary education, post secondary diploma/degree); household income level [low (< $50,000 CDN), medium (≥ $50,000 but < $100,000), high (≥ $100,000)]; chronic conditions (number of doctor diagnosed medical conditions; Supplementary Material Table A2); cognitive function [normal/abnormal; Montreal Cognitive Assessment (MoCA) score 0–22 whereby ≥ 19 is normal] [55]; race (white or non-white including mixed race); smoking (never, former, current); marital status (married or common law, single, divorced/separated/widowed). For alcohol, responses about daily, weekly and monthly frequency of standard drink consumption were categorised based on Canada’s low risk drinking guidelines [no risk (no drinks), low (≤ 2 drinks per week), moderate (3–6 drinks per week), high (≥ 7 drinks per week)] [56].

Analysis strategy

A posteriori power analysis was conducted indicating that the study sample had 100% power to detect small (0.02), medium (0.15) and large effects sizes (0.35) with α set at 0.05 (Supplementary Figure A1) [57]. Statistical analyses were performed using SPSS v 30.0 (IBM Corp, Armonk, USA).

CoDA was used to determine differences in waking-day movement behaviour composition according to the measures of mobility [58]. Geometric means for the proportion of time spent in each movement behaviour were calculated as they better represent the central tendency of compositional data than arithmetic means. The codependence between movement behaviours can then be assessed using pair-wise log ratio variances between all behaviours [(e.g., variance of ln (SB/MVPA)] and scaled to aid in interpretationInline graphic where t is any log-ratio variance]. Values for pair-wise log-ratio variances range from zero to one, with those closer to one indicating higher codependence. These values were then represented in a variation matrix.

Subsequently, movement behaviour variables were transformed from their natural space, the constrained simplex Sd onto real space where standard statistical techniques can be used. For this step, isometric log ratios (ilr) were used to express the waking-day movement behaviour composition as ratios of its parts (i.e., absolute time spent in SB, LIPA, MVPA). Sequential binary partitioning was used to determine the appropriate configuration of ilr coordinates for each movement behaviour, so that each one was assessed as the main behaviour in relation to the remaining movement behaviours (e.g., time spent in SB relative to LIPA and MVPA) [59, 60]. Waking-day movement behaviour composition allotted into three parts (SB, LIPA, MVPA) was expressed as two ilr coordinates that capture the combined distribution of all parts of the composition. For example, ilr coordinates for the relative contribution of MVPA were written as:

graphic file with name d33e921.gif

When transforming the values into ratios for CoDA, zero values are not tolerated (e.g., no time spent in MVPA). To address that, multiple behaviours are amalgamated into one or imputation of a minimal detectable value is used. However, in this study sample no zero values were present, thereby avoiding the zero issue [61].

Once movement behaviours were transformed, the two ilr coordinates of each movement behaviour were entered as the outcome variables in multivariate analysis of variance (MANOVA) models run for each mobility measure. The p-value associated with the first coordinate is the one that provides the relevant information of the numerator variable relative to the remaining movement behaviours [33]. The other coordinate variable is used to fit the model. If the MANOVA suggested rejecting the null hypothesis, Hotelling’s T-squared test was used to determine which pair of groups were different and D-1 simultaneous t-tests were used to determine which ilr coordinate was responsible for the difference [58]. To avoid an artificial increase of Type 1 error, the α level was set to 0.0167 using the Bonferroni correction [58]. The MANOVA results pertaining to the ilr coordinates were back-transformed to obtain the amount of time (hours: minutes) for that behaviour relative to the remaining behaviours in the mean waking-day composition. Detailed step-by-step instructions for CoDA analysis are provided elsewhere [62]. Confounding variables were tested against each movement behaviour using univariate linear regression. Those significantly associated with any behaviour based on a conservative p-value of < 0.2 were controlled for in the MANOVA models.

Sex and age stratified analyses were run (male/female; mean age split < 73.6 years ≥ 73.6 years) based on their a priori consideration as effect modifiers. The patterns of association were generally the same as the full sample; therefore, final analyses were run on the full sample with sex and age treated as confounding variables. Effect sizes from compositional MANOVA were used to evaluate the strength of association between mobility measures and differences in waking-day movement composition.

Results

The final study sample included 1,227 participants (mean age = 73.6 years, SD = 5.3). A detailed flowchart summarising participant inclusion is presented in Fig. 1. Participants had an average of 9.5 (SD = 1.5) valid days and waking-day wear time ranged from 10.5 (minimum) to 18.9 (maximum) hours. Characteristics of the final study sample are in Table 2. A higher number of women (69.5%) were studied. Most participants had post-secondary education (76.9%), medium income level (41.8%) and normal cognitive function (83.1%). Confounder testing showed race, alcohol, smoking and marital status were not associated with any of the three behaviours; therefore, these variables were excluded in the final MANOVA models. The effect size for each mobility measure is provided in Supplementary Material Table A3.

Fig. 1.

Fig. 1

Flowchart of study participants

Table 2.

Participant characteristics

Characteristic N or mean % or SD
Sex
 Male 374 30.5
 Female 852 69.5
Age (years) 73.6 5.3
BMI 26.2 4.7
Education level
 No post secondary education 284 23.1
 Post-secondary degree/diploma 943 76.9
Household income level
 Low 376 30.6
 Medium 513 41.8
 High 338 27.5
Chronic conditions (no.) 3.3 1.9
MoCA cognitive function score
 Normal 1,020 83.1
 Abnormal 207 16.9
Use of walking aid
 Yes 91 7.4
 No 1,136 92.6

BMI body mass index, MoCA Montreal Cognitive Assessment, SD Standard deviation

The compositional means for SB, LIPA, and MVPA were 10:43, 2:11, 0:36, respectively (hours: minutes; Table 3). The highest co-dependence between pair-wise log ratios was LIPA and SB (0.74). The lowest co-dependence was between MVPA and SB (0.30) (Table 4).

Table 3.

Descriptive characteristics of movement behaviours

Movement behaviour Arithmetic mean (SD) Median (IQR) Compositional mean
SB 10:49 (1:29) 10:49 (1:57) 10:43
LIPA 2:21 (0:48) 2:20 (1:07) 2:11
MVPA 0:47 (0:31) 0:40 (0:41) 0:36
Total 13:57 (1:10) 13:58 (1:33) 13:30

Data presented in hours: minutes

Table 4.

Variation matrix of correlations between movement behaviours

Movement behaviour SB LIPA MVPA
SB - 0.74 0.30
LIPA 0.74 - 0.73
MVPA 0.30 0.73 -

Descriptive characteristics of the mobility measures are in Table 5. Fifty-nine percent of participants (n = 731) were classified as having ‘no mobility limitation’ per the PCML. The median scores for the Physical Activity Scale for the Elderly (PASE) and LSA were 145.64 and 76, respectively. Median times were 8.85 s for the TUG, 12.28 s for the 5-Times Sit-to-Stand Test, and 4.63 min for the 400-meter walk test. Participants had a median gait speed of 1.26 m/second.

Table 5.

Description of self-report and performance-based mobility measures

Mobility Measures Median (IQR) or n
Self-report
Preclinical Mobility Limitation Scale, score of 0,1, or 2
 No mobility limitation (0) 731
 Preclinical mobility limitation (1) 200
 Minor manifest limitation (2) 296
Late-Life Function and Disability Instrument-Disability Component, score 0-100 (↑score = ↓ disability) 54.49 (51.51–58.95)

Late-Life Function and Disability Instrument-Physical Function Component, score 0-100

(↑ score = ↑ function)

68.10 (62.51–74.59)
Physical Activity Scale for the Elderly, score 0-400 or more 145.64 (103.40-194.59)
Life Space Assessment, score 0-120 76 (64–90)
Mobility Assessment Tool-short form†, score 30–80 64.14 (57.82–64.14)
Performance-based
Timed Up and Go (usual pace), seconds 8.85 (7.97–9.97)
Timed Up and Go (fast pace), seconds 6.31 (5.66–7.19)
Timed Up and Go (cognitive), seconds 9.22 (7.94–11.03)
Sit to Stand Test (5x), seconds 12.28 (10.53–14.37)
Gait speed (usual pace), meters/second 1.26 (1.10–1.39)
Gait speed (fast pace), meters/second 1.71 (1.55–1.87)
400-meter walk†, minutes 4.63 (4.23–5.14)
Single Leg Stance (right leg), seconds 17.38 (5.31–48.19)
Single Leg Stance (left leg), seconds 15.72 (5.12–45.47)
Stair-climbing power†, watts 247.58 (204.65-308.46)

†Tests performed only at Hamilton site. Sample sizes for the respective tests were n = 937; 899; and 919

Fifty-four associations reflecting three movement behaviours by 16 self-report and performance-based mobility measures and two indices were examined. Tables 6 and 7 present the back-transformed group means of time spent in each movement behaviour within each of the mobility measure groups, adjusted for age, sex, BMI, income level, education level, cognitive function, and number of chronic diseases. Table 8 presents a high-level summary of results for these associations to facilitate interpretation of overall patterns.

Table 6.

Model-adjusted compositional means of movement behaviours by tertile of self-reported mobility measures

Self-report measures SB LIPA MVPA
Self-report measures index
 Low 10:13 (10:03, 10:22)* 2:10 (2:07, 2:12) 0:42 (0:39, 0:45)
 Moderate 9:49 (9:38, 10:00) 2:24 (2:22, 2:27) 0:57 (0:53, 1:02)
 High 9:41 (9:31, 9:52) 2:29 (2:27, 2:31) 1:03 (0:59, 1:08)
Preclinical Mobility Limitation Scale
 No mobility limitation 9:53 (9:46, 9:59)* 2:22 (2:20, 2:23) 0:58 (0:55, 1:01)
 Preclinical mobility limitation 9:54 (9:43, 10:05) 2:22 (2:19, 2:24) 0:53 (0:49, 0:57)
 Minor limitation 10:12 (10:01, 10:22) 2:10 (2:08, 2:13) 0:44 (0:41, 0:48)*
Late-Life Function and Disability Instrument (disability component)
 Low 10:07 (9:59, 10:14)* 2:13 (2:12, 2:15) 0:48 (0:45, 0:51)*
 Moderate 9:46 (9:37, 9:55) 2:27 (2:25, 2:29) 0:58 (0:55, 1:02)
 High 9:57 (9:46, 10:07) 2:19 (2:17, 2:21) 0:56 (0:52, 1:00)
Late-Life Function and Disability Instrument (function component)
 Low 10:05 (9:55, 10:14)* 2:15 (2:13, 2:17) 0:47 (0:43, 0:50)*
 Moderate 9:54 (9:44, 10:03) 2:22 (2:19, 2:23) 0:54 (0:51, 0:58)
 High 9:52 (9:44, 10:00) 2:21 (2:20, 2:23)* 1:00 (0:56, 1:03)
Physical Activity Scale for the Elderly
 Low 10:27 (10:18, 10:34)* 1:59 (1:57, 2:01) 0:43 (0:41, 0:46)
 Moderate 9:59 (9:50, 10:07)* 2:19 (2:17, 2:21) 0:49 (0:46, 0:52)
 High 9:41 (9:32, 9:49)* 2:30 (2:28, 2:31) 1:03 (0:59, 1:06)*
Life-Space Assessment
 Low 10:02 (9:54, 10:10) 2:17 (2:15, 2:19) 0:49 (0:46, 0:52)
 Moderate 10:02 (9:54, 10:10) 2:16 (2:14, 2:17) 0:53 (0:50, 0:56)
 High 9:47 (9:31, 9:56) 2:25 (2:23, 2:27) 1:01 (0:58, 1:05)
Mobility Assessment Tool-short form
 Low 10:11 (10:04, 10:18)* 2:11 (2:09, 2:13) 0:44 (0:42, 0:47)*
 Moderate 9:53 (9:43, 10:02) 2:22 (2:19, 2:25) 0:56 (0:51, 1:01)
 High 9:49 (9:40, 9:59) 2:30 (2:27, 2:32) 1:00 (0:55, 1:05)

Data presented in hours:minutes(95%CI). Groups statistically significant from remaining groups are bolded and include an * symbol (p < 0.0167). Adjusted for age, sex, BMI, income level, education level, MoCA score, and number of chronic diseases. Interpretation example: Participants in the low tertile of the self-report measures index spent significantly more daily time in SB (10:13) compared to those in the moderate (9:49) and high (9:41) tertiles. ‘Low’, ‘moderate’, and ‘high’ refer to tertiles within each measure; interpretation differs depending on whether higher or lower values reflect better mobility performance

Table 7.

Model-adjusted compositional means of movement behaviours by tertile of performance-based mobility measures

Performance-based measures SB LIPA MVPA
Performance-based measures index
 Low 9:36 (9:22, 9:48)* 2:32 (2:30, 2:35) 1:07 (1:02, 1:13)*
 Moderate 10:13 (10:03, 10:22) 2:10 (2:07, 2:12) 0:47 (0:41, 0:48)
 High 10:04 (9:55, 10:09) 2:15 (2:13, 2:18) 0:49 (0:45, 0:52)
Timed Up and Go (usual pace)
 Low 9:45 (9:36, 9:54)* 2:26 (2:24, 2:27) 1:03 (1:00, 1:07)*
 Moderate 10:03 (9:54, 10:12) 2:15 (2:13, 2:17) 0:51 (0:48, 0:55)
 High 10:13 (10:04, 10:22) 2:09 (2:07, 2:11) 0:45 (0:42, 0:49)
Timed Up and Go (fast pace)
 Low 9:45 (9:35, 9:54) 2:26 (2:24, 2:27) 1:03 (0:59, 1:07)
 Moderate 9:58 (9:48, 10:07) 2:19 (2:17, 2:20) 0:54 (0:51, 0:58)
 High 10:19 (10:11, 10:27)* 2:06 (2:04, 2:07) 0:41 (0:39, 0:44)*
Timed Up and Go (cognitive)
 Low 9:38 (9:27, 9:49)* 2:29 (2:27, 2:31) 1:09 (1:04, 1:14)*
 Moderate 10:02 (9:53, 10:11) 2:16 (2:14, 2:18) 0:52 (0:48, 0:55)
 High 10:11 (10:04, 10:18) 2:11 (2:09, 2:12) 0:45 (0:43, 0:48)
Sit to Stand Test (5x)
 Low 9:44 (9:35, 9:53) 2:27 (2:25, 2:29) 1:02 (0:58, 1:06)
 Moderate 9:57 (9:47, 10:06) 2:19 (2:17, 2:22) 0:54 (0:51, 0:58)
 High 10:14 (10:06, 10:21)* 2:09 (2:07, 2:10) 0:45 (0:42, 0:47)*
Gait Speed (usual pace)
 Low 10:18 (10:09, 10:27)* 2:06 (2:03, 2:08) 0:43 (0:40, 0:46)*
 Moderate 9:55 (9:37, 10:03) 2:21 (2:19, 2:22) 0:55 (0:52, 0:59)
 High 9:40 (9:29, 9:51) 2:30 (2:28, 2:31) 1:04 (1:00, 1:09)
Gait Speed (fast pace)
 Low 10:13 (10:04, 10:21) 2:10 (2:08, 2:12) 0:43 (0:40, 0:46)*
 Moderate 10:01 (9:51, 10:11) 2:16 (2:14, 2:18) 0:54 (0:50, 0:57)*
 High 9:37 (9:27, 9:47)* 2:31 (2:29, 2:33) 1:07 (1:03, 1:11)*
400-meter walk test
 Low 9:24 (9:11, 9:36)* 2:39 (2:37, 2:41) 1:14 (1:09, 1:20)*
 Moderate 9:51 (9:40, 10:01)* 2:24 (2:22, 2:26) 0:54 (0:51, 0:59)*
 High 10:22 (10:15, 10:30)* 2:03 (2:00, 2:05) 0:37 (0:35, 0:40)*
Single Leg Stance (right leg)
 Low 10:09 (10:01, 10:17) 2:12 (2:10, 2:14) 0:47 (0:44, 0:50)*
 Moderate 9:55 (9:46, 10:04) 2:21 (2:19, 2:22) 0:55 (0:52, 0:59)
 High 9:48 (9:37, 9:58) 2:25 (2:23, 2:27) 0:58 (0:54, 1:02)
Single Leg Stance (left leg)
 Low 10:08 (10:01, 10:17) 2:12 (2:11, 2:14) 0:47 (0:42, 0:49)
 Moderate 10:00 (9:51, 10:09) 2:17 (2:15, 2:19) 0:52 (0:49, 0:56)
 High 9:53 (9:43, 10:03) 2:21 (2:19, 2:23) 0:58 (0:54, 1:02)
Stair-climbing power
 Low 10:33 (10:21, 10:44)* 1:56 (1:52, 1:59) 0:38 (0:34, 0:42)*
 Moderate 10:01 (9:49, 10:11) 2:17 (2:14, 2:20) 0:53 (0:45, 0:57)
 High 9:45 (9:32, 9:57) 2:28 (2:25, 2:31) 0:59 (0:54, 1:04)

Data presented in hours:minutes(95%CI). Groups statistically significant from remaining groups are bolded and include an * symbol (p < 0.0167). Adjusted for age, sex, BMI, income level, education level, MoCA score, and number of chronic diseases. Interpretation example: Participants in the ‘low’ tertile of Timed-Up and Go (usual pace) spent significantly less daily time in SB (9:45) compared to the moderate (10:03) and high (10:13) tertiles. ‘Low’, ‘moderate’, and ‘high’ refer to tertiles within each measure; interpretation differs depending on whether higher or lower values reflect better mobility performance

Table 8.

Summary of results of the associations between mobility measures and movement behaviours relative to one another

Mobility measure SB LIPA MVPA
Self-report measures index ↓ ↔ ↑
Preclinical Mobility Limitation Scale ↑ ↔ ↓

Late-Life Function and Disability Instrument-

disability component

↓ ↔ ↑

Late-Life Function and Disability Instrument-

function component

↓ ↑ ↑
Physical Activity Scale for the Elderly ↓ ↔ ↑
Life Space Assessment ↔ ↔ ↔
Mobility Assessment Tool-Short Form ↓ ↔ ↑
Performance-based measures index ↑ ↔ ↓
Timed Up and Go (usual pace) ↑ ↔ ↓
Timed Up and Go (fast pace) ↑ ↔ ↓
Timed Up and Go (cognitive) ↑ ↔ ↓
Repeated Chair-Stand ↑ ↔ ↓
Gait speed (usual pace) ↓ ↔ ↑
Gait speed (fast pace) ↓ ↔ ↑
400-meter walk test ↑ ↔ ↓
Single-Leg Stance, right leg ↔ ↔ ↑
Single-Leg Stance, left leg ↔ ↔ ↔
Stair-Climbing Power ↓ ↔ ↑

↑ indicates a significant positive association, ↓ indicates a significant negative association, ↔ indicates a non-significant association (p < 0.0167 for all)

There were significant differences in waking-day movement behaviour composition across tertiles of the self-report and performance-based mobility measures and indices. Older adults with lower mobility consistently demonstrated more SB and less MVPA per day across all self-report measures except LSA. For instance, those in the low PASE tertile accumulated an additional 46 min/day of SB compared to the high tertile (p < 0.001). Conversely, those in the high PASE tertile accumulated 20 more minutes/day of MVPA than those in the low tertile (p < 0.001). The best performing self-report measure for explaining waking-day movement behaviour composition was the PASE (partial η2 = 0.03, p < 0.001).

For all performance-based measures except the single leg stance, older adults with better mobility consistently demonstrated lower daily SB and higher MVPA. The three TUG tests showed that those in the low tertile (i.e., faster completion times, indicating better performance) spent less time in SB per day compared to the high tertile. For instance, the low TUG usual pace tertile had 28 fewer minutes/day of SB than the high tertile (p < 0.001). Conversely, that same tertile accumulated 18 more minutes/day of MVPA compared to the high tertile (p < 0.001). The 400-meter walk test was the most consistent performance-based measure showing significant differences across all tertiles for both SB and MVPA. For SB, participants in the low tertile (fastest completion times) spent 27 and 58 fewer minutes/day than the moderate (p < 0.001) and high (p < 0.001) tertiles, respectively. For MVPA, those in the low tertile accumulated 20 and 37 more minutes/day than the moderate (p < 0.001) and high (p < 0.001) tertiles, respectively. The 400-meter walk test was also the best performance-based measure for capturing waking-day movement behaviour composition (partial η² = 0.07, p < 0.001).

The LLFDI function component was the only measure to show significant group differences in LIPA. Older adults in the high tertile accumulated six more minutes/day of LIPA compared to the low tertile (p = 0.017).

Both self-report and performance-based measure indices demonstrated significant group differences in daily SB and MVPA. However, the self-reported measures index showed greater differences in both behaviours. For SB, the low tertile of the self-reported index had 32 fewer minutes/day than the high tertile (p < 0.001) compared to 28 fewer minutes/day for the performance-based measures index (p < 0.001). For MVPA, the low tertile of the self-reported measures index had 21 fewer minutes/day than the high tertile (p < 0.001), while it was 18 fewer minutes/day for the performance-based measures index (p < 0.001). Both indices had the same effect size for capturing waking-day movement behaviour composition (partial η² = 0.02, p < 0.001).

Discussion

To our knowledge, this is the first study to use CoDA to examine associations between commonly used self-report and performance-based mobility measures, and the waking-day movement behaviour composition in older adults. Differences in waking-day movement behaviour composition were found across the self-report and performance-based mobility measures. Older adults with lower mobility consistently accumulated more SB and less MVPA throughout the day. However, the association with different movement behaviours varied depending on the specific measure, with the PASE and 400-meter walk test identified as the best self-report and performance-based measures. Overall, the observed associations between the mobility measures and waking-day movement behaviours support the validity of commonly used mobility measures in identifying meaningful differences in daily movement behaviour composition; however, the small effect sizes indicate limited ability to explain or predict real-world mobility. Differences ranged from small (e.g., 1 min/day of LIPA or about 0.01% difference) to large (58 min/day of SB or about 7% difference), followed a graded pattern across tertiles and were directionally consistent (e.g., SB was highest in the lowest gait speed tertile).

While it is difficult to directly compare findings from studies using conventional statistics with those derived from CoDA, ours showed that both self-report and performance-based measures of mobility are related to device-derived waking-day movement behaviour composition. Among the performance-based measures, the most demanding tests of physical capacity, namely the 400-meter walk, and fast gait speed were the most sensitive indicators of how older adults spend their time in waking-day movement behaviours. Similar results on the relationship between these two tests and accelerometer derived daily physical activity have been found in other studies. For instance, we observed a strong and consistent negative association between 400-meter walk times and accumulated daily MVPA across low, moderate, and high tertiles. A study examining a sample of German older adults (mean age = 80.8 years) found that faster 400-meter walk time is associated with higher daily step count (β = -6.4, 95%CI: -9.99, -3.3) and cadence (β = -0.018, 95%CI: -0.028, -0.009) [63]. Further, we observed a similar relationship between fast gait speed and daily MVPA across all tertiles in our sample. A study assessing older adults with a mean age of 73 years found a similar negative association between fast gait speed and daily MVPA in women (β = 0.24, 95%CI: 0.18, 0.30) and men (β = 0.18, 95%CI: 0.07, 0.20) [28]. Our results suggest faster walk completion time and higher gait speed are associated with meaningful increase in daily MVPA. Furthermore, the effect sizes of these two tests, although modest, were the largest estimates among those we tested, suggesting they may be more informative over the other measures. One possible explanation is that these tests involve sustained and purposeful movement, an essential component of daily activity in older adults, as opposed to brief or static assessments that take place in a controlled setting (e.g., single leg balance). Moreover, they integrate multiple physiological systems, namely anaerobic and aerobic capacity, lower limb strength, dynamic balance and stability, all of which are important for real-world mobility. These stronger associations may therefore reflect construct alignment with device-detected ambulatory activity, rather than true superiority as indicators of overall mobility [64].

We observed numerous significant associations between mobility level and waking-day movement behaviours, particularly among individuals in the lowest performing tertiles and their engagement in daily SB with 10 of the 18 mobility measures showing significant associations. Notably, the PASE and 400-meter walk test were the strongest measures of daily SB and demonstrated the greatest magnitude in differences whereby individuals in the lowest performing tertile spent on average, 45 more minutes per day in SB compared to the highest tertile. Our finding that PASE strongly explains daily SB differs from previous studies [65–67]. For instance, a study assessing American older adults (median age = 71 years) found no significant relationship between PASE score and accelerometry derived total SB minutes per day (r = 0.04, p = 0.699) [67]. The strong negative association we observed between PASE score and daily SB suggest that PASE may have greater utility in capturing differences in SB when analysed using CoDA, because it accounts for the important co-dependence between movement behaviours that is not considered with traditional statistical methods.

A noteworthy observation of this study is that none of the mobility measures showed a significant association with LIPA, with the one exception being a marginal association observed in the highest tertile on the LLFDI-function component. The current literature on the relationship between mobility performance and daily time spent in LIPA is conflicting [25, 26, 68–70]. Using a CoDA framework, our study is the first to demonstrate no meaningful relationship between either self-report and performance-based measures of mobility and daily LIPA. The lack of observed association may reflect a systematic measurement issue in existing tools, that may not be sensitive enough to detect light intensity and incidental physical activity. The increasing credence given to LIPA in movement behaviour guidelines and public health messaging aimed at older adults [22, 71, 72], many of whom may be unwilling or unable to perform MVPA highlights there is a need to evaluate mobility with more ecologically valid tools. For instance, going beyond conventionally accepted minimum wear times or wearing both wrist and thigh accelerometers simultaneously may be necessary to enhance estimates of older adults’ real-world mobility.

Our results must be interpreted in light of the limitations. First, the cross-sectional design precludes making causal inferences. Further, the findings may be most generalisable to higher functioning older adults as the median values for TUG, gait speed and 400-meter walk test indicated above-average physical performance [44, 73, 74] consistent with a sample of older adults without major mobility limitations at baseline [37]. Also, the study addressed waking-day movement behaviour composition, as data on sleep was not collected. This approach is consistent with other CoDA studies that did not have sleep data [75]. Further studies that include the full 24-h movement profile are needed to validate our findings. Last, although accelerometers provide direct measures of movement behaviours, wrist-worn devices cannot accurately capture posture (e.g., sitting vs. standing), which may lead to some misclassification between SB and LIPA and attenuate effect estimates [76]. While we have shown that certain self-report and performance-based mobility measures, specifically PASE, 400-meter walk test, and fast gait speed, perform well for capturing the waking-day movement behaviour composition in relation to MVPA and SB, the next step is to extend these observations to a more diverse sample using longitudinal study design that also considers device-based measures of mobility.

Conclusion

In summary, traditional self-report and performance-based mobility measures were associated with the waking-day movement behaviour composition in older adults; however, the small effect sizes indicate a limited ability to fully capture real-world behaviour. There was a graded pattern across mobility level and daily time spent in SB and MVPA, respectively. The PASE, 400-meter walk and fast gait speed tests offered the clearest indication of how older adults distribute their time across waking-day movement behaviours. Overall, our findings raise important questions about the applicability of traditional mobility measures for making inferences about real-world mobility. None of the 18 tested measures captured daily LIPA despite being the activity intensity older adults spend the most of their time in. Future studies should use CoDA to evaluate other potential mobility measures, including device-based metrics, and their relationship with the daily movement behaviour composition in older adults.

Supplementary Information

12966_2026_1939_MOESM1_ESM.docx (225.4KB, docx)

Additional file 1: Table A1. Boundary values between the low, moderate and high tertiles for each mobility measure. Table A2. Self-reported chronic conditions diagnosed by a doctor for chronic conditions variable. Table A3. Partial η² effect sizes of self-report and performance-based mobility measures in capturing waking-day movement behaviour composition. Figure A1. Results of power analysis.

Acknowledgements

We would like to thank software engineer Cody Cooper and the NiMBaLWear team for processing the data and supporting dataset preparation and access.

Abbreviations

AVM

Average vector magnitude

BMI

Body mass index

CI

Confidence interval

CoDA

Compositional data analysis

DETACH

Device Temperature and Accelerometer Change

ICF

International Classification of Functioning, Disability and Health

ilr

Isometric log ratio

IQR

Interquartile range

LIPA

Light-intensity physical activity

LLFDI

Late-Life Function and Disability Instrument

LSA

Life Space Assessment

MacM3

McMaster Monitoring my Mobility study

MANOVA

Multivariate analysis of variance

MoCA

Montreal Cognitive Assessment

MVPA

Moderate-to-vigorous physical activity

PASE

Physical Activity Scale for the Elderly

PCML

Preclinical Mobility Limitation

SB

Sedentary behaviour

SD

Standard deviation

TUG

Timed Up and Go

Authors’ contributions

SH and MKB conceived the study. SH performed the analysis. RK contributed to the acquisition of data. SH, RK, SMP, RZ and MKB contributed to the analysis and interpretation of findings. SH drafted the manuscript with critical revision by MKB, RK, SMP, and RZ. All authors approved the final manuscript. MKB is the guarantor. The corresponding author attests that all listed authors meet authorship criteria and that no others meeting the criteria were omitted.

Funding

SH is funded by the McMaster Institute for Research on Aging post-doctoral fellowship program; MKB holds a Tier 2 Canada Research Chair in Mobility, Aging, and Chronic Disease (CRC-2020-00043) and an Early Researcher Award from the Government of Ontario. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Data availability

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Declarations

Ethics approval and consent to participate

This study was approved by the Hamilton Integrated Research Ethics Board (HiREB), McMaster University (Project number #: 13905).

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.Middleton A, Fritz SL, Lusardi M. Walking speed: the functional vital sign. J Aging Phys Act. 2015;23(2):314–22. 10.1123/japa.2013-0236. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Penninx BWJH, Ferrucci L, Leveille SG, Rantanen T, Pahor M, Guralnik JM. Lower extremity performance in nondisabled older persons as a predictor of subsequent hospitalization. J Gerontol Biol Sci Med Sci. 2000;55(11):M691–7. 10.1093/gerona/55.11.m691. [DOI] [PubMed] [Google Scholar]
  • 3.Reijnierse EM, Geelen SJG, van der Schaaf M, Visser B, Wüst RCI, Pijnappels M, et al. Towards a core-set of mobility measures in ageing research: the need to define mobility and its constructs. BMC Geriatr. 2023;23(1):220. 10.1186/s12877-023-03859-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.World Health Organization. World report on ageing and health. Geneva: World Health Organization; 2015. [Google Scholar]
  • 5.World Health Organization. International Classification of Functioning, Disability and Health. Geneva: World Organization; 2018. [Google Scholar]
  • 6.Beauchamp M, Hao Q, Kuspinar A, Alder G, Makino K, Nouredanesh M, et al. Measures of perceived mobility ability in community-dwelling older adults: a systematic review of psychometric properties. Age Ageing. 2023;52(Supplement4):iv100–11. 10.1093/ageing/afad124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Kuspinar A, Mehdipour A, Beauchamp MK, Hao Q, Cino E, Mikton C, et al. Assessing the measurement properties of life-space mobility measures in community-dwelling older adults: a systematic review. Age Ageing. 2023;52(Supplement4):iv86–99. 10.1093/ageing/afad119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Honvo G, Sabico S, Veronese N, Bruyère O, Rizzoli R, Amuthavalli Thiyagarajan J, et al. Measures of attributes of locomotor capacity in older people: a systematic literature review following the COSMIN methodology. Age Ageing. 52(Supplement_4):iv44–66. 10.1093/ageing/afad139. [DOI] [PMC free article] [PubMed]
  • 9.Coman L, Richardson J. Relationship between self-report and performance measures of function: a systematic review. Can J Aging. 2006;25(3):253–70. 10.1353/cja.2007.0001. [DOI] [PubMed] [Google Scholar]
  • 10.Pinto-Carral A, Fernández-Villa T, de la Molina AJ. Patient-reported mobility: a systematic review. Arch Phys Med Rehabil. 2016;97(7):1182–94. 10.1016/j.apmr.2016.01.025. [DOI] [PubMed] [Google Scholar]
  • 11.Boissy P, Blamoutier M, Brière S, Duval C. Quantification of free-living community mobility in healthy older adults using wearable sensors. Front Public Health. 2018;6. 10.3389/fpubh.2018.00216. [DOI] [PMC free article] [PubMed]
  • 12.Giannouli E, Bock O, Mellone S, Zijlstra W. Mobility in old age: capacity is not performance. Biomed Res Int. 2016;(1):3261567. 10.1155/2016/3261567. [DOI] [PMC free article] [PubMed]
  • 13.Martin P, Keppler AM, Alberton P, Neuerburg C, Drey M, Böcker W, et al. Self-assessment of mobility of people over 65 years of age. Medicina. 2021;57(9):980. 10.3390/medicina57090980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Mikolaizak AS, Rochester L, Maetzler W, Sharrack B, Demeyer H, Mazzà C, et al. Connecting real-world digital mobility assessment to clinical outcomes for regulatory and clinical endorsement–the Mobilise-D study protocol. PLoS ONE. 2022;17(10):e0269615. 10.1371/journal.pone.0269615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Ó Breasail M, Biswas B, Smith MD, Mazhar MKA, Tenison E, Cullen A, et al. Wearable GPS and accelerometer technologies for monitoring mobility and physical activity in neurodegenerative disorders: a systematic review. Sensors. 2021;21(24). 10.3390/s21248261. [DOI] [PMC free article] [PubMed]
  • 16.Vogel T, Brechat PH, Leprêtre PM, Kaltenbach G, Berthel M, Lonsdorfer J. Health benefits of physical activity in older patients: a review. Int J Clin Pract. 2009;63(2):303–20. 10.1111/j.1742-1241.2008.01957.x. [DOI] [PubMed] [Google Scholar]
  • 17.Sun F, Norman IJ, While AE. Physical activity in older people: a systematic review. BMC Public Health. 2013;13(1):449. 10.1186/1471-2458-13-449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Prince SA, Elliott CG, Scott K, Visintini S, Reed JL. Device-measured physical activity, sedentary behaviour and cardiometabolic health and fitness across occupational groups: a systematic review and meta-analysis. Int J Behav Nutr Phys Act. 2019;16(1):30. 10.1186/s12966-019-0790-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Füzéki E, Engeroff T, Banzer W. Health benefits of light-intensity physical activity: a systematic review of accelerometer data of the national health and nutrition examination survey (NHANES). Sports Med. 2017;47(9):1769–93. 10.1007/s40279-017-0724-0. [DOI] [PubMed] [Google Scholar]
  • 20.Gennuso KP, Gangnon RE, Matthews CE, Thraen-Borowski KM, Colbert LH. Sedentary behavior, physical activity, and markers of health in older adults. Med Sci Sports Exerc. 2013;45(8):1493–500. 10.1249/mss.0b013e318288a1e5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Sansano-Nadal O, Giné-Garriga M, Rodríguez-Roca B, Guerra-Balic M, Ferri K, Wilson JJ, et al. Association of self-reported and device-measured sedentary behaviour and physical activity with health-related quality of life among European older adults. Int J Environ Res Public Health. 2021;18(24). 10.3390/ijerph182413252. [DOI] [PMC free article] [PubMed]
  • 22.Ross R, Chaput JP, Giangregorio LM, Janssen I, Saunders TJ, Kho ME, 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):S57–102. 10.1139/apnm-2020-0467. [DOI] [PubMed] [Google Scholar]
  • 23.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 Nutri Metab. 2020;45(10):S248–57. 10.1139/apnm-2020-0160. [DOI] [PubMed] [Google Scholar]
  • 24.Ciprandi D, Bertozzi F, Zago M, Ferreira CLP, Boari G, Sforza C, et al. Study of the association between gait variability and physical activity. Eur Rev Aging Phys Act. 2017;14(1):19. 10.1186/s11556-017-0188-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.van Lummel RC, Walgaard S, Pijnappels M, Elders PJM, Garcia-Aymerich J, van Dieën JH, et al. Physical performance and physical activity in older adults: associated but separate domains of physical function in old age. PLoS ONE. 2015;10(12):e0144048. 10.1371/journal.pone.0144048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Fini NA, Bernhardt J, Holland AE. Low gait speed is associated with low physical activity and high sedentary time following stroke. Disabil Rehabil. 2021;43(14):2001–8. 10.1080/09638288.2019.1691273. [DOI] [PubMed] [Google Scholar]
  • 27.Rasinaho M, Hirvensalo M, Leinonen R, Lintunen T, Rantanen T. Motives for and barriers to physical activity among older adults with mobility limitations. J Aging Phys Act. 2007;15(1):90–102. 10.1123/japa.15.1.90. [DOI] [PubMed] [Google Scholar]
  • 28.Egerton T, Paterson K, Helbostad JL. The association between gait characteristics and ambulatory physical activity in older people: a cross-sectional and longitudinal observational study using Generation 100 data. J Aging Phys Act. 2017;25(1):10–9. 10.1123/japa.2015-0252. [DOI] [PubMed] [Google Scholar]
  • 29.Nicolai S, Benzinger P, Skelton DA, Aminian K, Becker C, Lindemann U. Day-to-day variability of physical activity of older adults living in the community. J Aging Phys Act. 2010;18(1):75–86. 10.1123/japa.18.1.75. [DOI] [PubMed] [Google Scholar]
  • 30.Pedišić Ž. Measurement issues and poor adjustments for physical activity and sleep undermine sedentary behaviour research-the focus should shift to the balance between sleep, sedentary behaviour, standing and activity. Kinesiology. 46(1):135–46. https://hrcak.srce.hr/123743.
  • 31.Pedišić Ž, Dumuid D, Olds TS. Integrating sleep, sedentary behaviour, and physical activity research in the emerging field of time-use epidemiology: Definitions, concepts, statistical methods, theoretical framework, and future directions. Kinesiology. 2017;49(2):252–69. https://ojs.srce.hr/index.php/kinesiology/article/view/5401. [Google Scholar]
  • 32.Dumuid D, Stanford TE, Martin-Fernández JA, Pedišić Ž, Maher CA, Lewis LK, et al. Compositional data analysis for physical activity, sedentary time and sleep research. Stat Methods Med Res. 2017;27(12):3726–38. 10.1177/0962280217710835. [DOI] [PubMed] [Google Scholar]
  • 33.Chastin SFM, 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. 10.1371/journal.pone.0139984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Beauchamp M, Kirkwood R, Cooper C, Brown M, Newbold KB, Scott D, et al. Monitoring mobility in older adults using a Global Positioning System (GPS) smartwatch and accelerometer: a validation study. PLoS ONE. 2023;18(12):e0296159. 10.1371/journal.pone.0296159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Mänty M, Heinonen A, Leinonen R, Törmäkangas T, Sakari-Rantala R, Hirvensalo M, et al. Construct and predictive validity of a self-reported measure of preclinical mobility limitation. Arch Phys Med Rehabil. 2007;88(9):1108–13. 10.1016/j.apmr.2007.06.016. [DOI] [PubMed] [Google Scholar]
  • 36.McMaster Institute for Research on Aging. Intergenerational Study on Aging (MIRA-iGeN. Building a platform for intergenerational research. Hamilton: McMaster Institute for Research on Aging; 2025. https://mira.mcmaster.ca/projects/intergenerational-study-on-aging-mira-igen-building-a-platform-for-intergenerational-research/. [Google Scholar]
  • 37.Beauchamp MK, Kirkwood R, Cooper C, McIlroy W, Van Ooteghem K, Beyer K, et al. Cohort profile: baseline characteristics and design of the McMaster Monitoring My Mobility (MacM3) Study, a prospective digital mobility cohort of community-dwelling older Canadians from Southern Ontario. BMJ Open. 2025;15(10):e105223. 10.1136/bmjopen-2025-105223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Altman DG, Bland JM, Statistics Notes. Quartiles, quintiles, centiles, and other quantiles. BMJ. 1994;309(6960):996. 10.1136/bmj.309.6960.996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Haley SM, Jette AM, Coster WJ, Kooyoomjian JT, Levenson S, Heeren T, et al. Late Life Function and Disability Instrument: II. development and evaluation of the function component. J Gerontol A Biol Sci Med Sci. 2002;57(4):217–22 10.1093/gerona/57.4.M217. [DOI] [PubMed]
  • 40.Jette AM, Haley SM,Coster WJ, Kooyoomjian JT, Levenson S, Heeren T, et al. Late Life Function and Disability Instrument: I. development and evaluation of the disability component. J Gerontol A Biol Sci Med Sci. 2002;57(4):209–16. 10.1093/gerona/57.4.M209. [DOI] [PubMed]
  • 41.Washburn RA, Smith KW, Jette AM, Janney CA. The physical activity scale for the elderly (PASE): development and evaluation. J Clin Epidemiol. 1993;46(2):153–62. 10.1016/0895-4356(93)90053-4. [DOI] [PubMed]
  • 42.Baker PS, Bodner EV, Allman RM. Measuring life-space mobility in community-dwelling older adults. J Am Geriatr Soc. 2003;51(11):1610–4. 10.1046/j.1532-5415.2003.51512.x. [DOI] [PubMed]
  • 43.Rejeski WJ, Rushing J, Guralnik JM, Ip EH, King AC, Manini TM, et al. The MAT-sf: identifying risk for major mobility disability. J Gerontol A Biol Sci Med Sci. 2015;70(5):641–6. 10.1093/gerona/glv003. [DOI] [PMC free article] [PubMed]
  • 44.Barry E, Galvin R, Keogh C, Horgan F, Fahey T. Is the Timed Up and Go test a useful predictor of risk of falls in community dwelling older adults: a systematic review and meta- analysis. BMC Geriatr. 2014;14(1):14. 10.1186/1471-2318-14-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Jones CJ, RikliRE, Beam WC. A 30-s chair-stand test as a measure of lower body strength in community-residing older adults. Res Q Exerc Sport. 1999;70(2):113–9. 10.1080/02701367.1999.10608028. [DOI] [PubMed]
  • 46.Abellan Van Kan G, Rolland Y, Andrieu S, Bauer J, Beauchet O, Bonnefoy M, et al. Gait speed at usual pace as a predictor of adverse outcomes in community-dwelling older people an International Academy on Nutrition and Aging (IANA) Task Force. J Nutr Health Aging. 2009;13(10):881–9. 10.1007/s12603-009-0246-z. [DOI] [PMC free article] [PubMed]
  • 47.Bohannon RW. Comfortable and maximum walking speed of adults aged 20-79 years: reference values and determinants. Age Ageing. 1997;26(1):15–9 10.1093/ageing/26.1.15. [DOI] [PubMed]
  • 48.Georgiopoulou VV, Kalogeropoulos AP, Chowdhury R, Binongo JNG, Bibbins-Domingo K, et al. Exercise capacity, heart failure risk, and mortality in older adults: the Health ABC Study. Am J Prev Med. 2017;52(2):144–53. 10.1016/j.amepre.2016.08.041. [DOI] [PMC free article] [PubMed]
  • 49.Springer BA, Marin R, Cyhan T, Roberts H, Gill NW. Normative values for the unipedal stance test with eyes open and closed. J Geriatr Phys Ther. 2007;30(1). 10.1519/00139143-200704000-00003. [DOI] [PubMed]
  • 50.Bean JF, Kiely DK, LaRose S, Alian J, Frontera WR. Is stair climb power a clinically relevant measure of leg power impairments in at-risk older adults? Arch Phys Med Rehabil. 2007;88(5):604–9. 10.1016/j.apmr.2007.02.004. [DOI] [PubMed]
  • 51.Beyer KB, Weber KS, Cornish BF, Vert A, Thai V, Godkin FE, et al. NiMBaLWear analytics pipeline for wearable sensors: a modular, open-source platform for evaluating multiple domains of health and behaviour. BMC Digit Health. 2024;2(1):8. 10.1186/s44247-024-00062-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Fraysse F, Post D, Eston R, Kasai D, Rowlands AV, Parfitt G. Physical activity intensity cut-points for wrist-worn GENEActiv in older adults. Front Sports Act Living. 2021. 10.3389/fspor.2020.579278. 2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.van Hees VT, Gorzelniak L, Dean León EC, Eder M, Pias M, Taherian S, 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]
  • 54.Colley R, Connor Gorber S, Tremblay MS. Quality control and data reduction procedures for accelerometry-derived measures of physical activity. Health Rep. 2010;21(1):63–9. https://www150.statcan.gc.ca/n1/en/pub/82-003-x/2010001/article/11066-eng.pdf?st=zQyg2eKN. [PubMed] [Google Scholar]
  • 55.Nasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I, et al. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005;53(4):695–9. 10.1111/j.1532-5415.2005.53221.x. [DOI] [PubMed] [Google Scholar]
  • 56.Canadian Centre on Substance Use and Addiction. Canada’s guidance on alcohol and health: final report. Ottawa: Canadian Centre on Substance Use and Addiction. 2023. https://www.ccsa.ca/sites/default/files/2023-01/CCSA_Canadas_Guidance_on_Alcohol_and_Health_Final_Report_en.pdf.
  • 57.Faul F, Erdfelder E, Lang AG, Buchner A. G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods. 2007;39(2):175–91. 10.3758/bf03193146. [DOI] [PubMed] [Google Scholar]
  • 58.Martín-Fernández JA, Daunis-i-Estadella J, Mateu-Figueras G. On the interpretation of differences between groups for compositional data. SORT-Statistics Oper Res Trans. 2015;39(2 SE–):231–52. https://www.idescat.cat/sort/sort392/39.2.4.martin-etal.pdf. [Google Scholar]
  • 59.McGregor DE, Palarea-Albaladejo J, Dall PM, Del Pozo Cruz B, Chastin SF. Compositional analysis of the association between mortality and 24-hour movement behaviour from NHANES. Eur J Prev Cardiol. 2021;28(7):791–98. 10.1177/2047487319867783. [DOI] [PubMed] [Google Scholar]
  • 60.Egozcue JJ, Pawlowsky-Glahn V. Groups of parts and their balances in compositional data analysis. Math Geol. 2005;37(7):795–828. 10.1007/s11004-005-7381-9. [DOI] [Google Scholar]
  • 61.Foley L, Dumuid D, Atkin AJ, Olds T, Ogilvie D. Patterns of health behaviour associated with active travel: a compositional data analysis. Int J Behav Nutr Phys Act. 2018;15(1):26. 10.1186/s12966-018-0662-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Chastin SFM, Palarea-Albaladejo J. Concise guide to compositional data analysis for physical activity, sedentary behaviour and sleep research: Supplementary Material S2, in Chastin SFM, 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. 10.1371/journal.pone.0139984. [DOI] [PMC free article] [PubMed]
  • 63.Rogler J, Krumpoch S, Freiberger E, Lindemann U, Kob R. Association between the 400-m walk test and sensor-based daily physical activity in frail and sarcopenic older adults. Eur Geriatr Med. 2025;16(5):1799–810. 10.1007/s41999-025-01262-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Liu F, Wanigatunga AA, Schrack JA. Assessment of physical activity in adults using wrist accelerometers. Epidemiol Rev. 2021;43(1):65–93. 10.1093/epirev/mxab004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Liu RDK, Buffart LM, Kersten MJ, Spiering M, Brug J, van Mechelen W, et al. Psychometric properties of two physical activity questionnaires, the AQuAA and the PASE, in cancer patients. BMC Med Res Methodol. 2011;11(1):30. 10.1186/1471-2288-11-30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Giray E. Comparative validity of Physical Activity Scale for Elderly with an accelerometer in patients with stroke. Geriatri. 2022;25(2):215–22. 10.31086/tjgeri.2022.278. [DOI] [Google Scholar]
  • 67.Hopkins J, McVeigh JA, Hill KD, Burton E. Physical activity levels and sedentary behavior of people living with mild cognitive impairment: a cross-sectional study using thigh-worn accelerometers. J Aging Phys Act. 2024;32(4):520–30. 10.1123/japa.2023-0176. [DOI] [PubMed] [Google Scholar]
  • 68.Rava A, Pihlak A, Kums T, Purge P, Pääsuke M, Jürimäe J. Associations of distinct levels of physical activity with mobility in independent healthy older women. Exp Gerontol. 2018;110:209–15. 10.1016/j.exger.2018.06.005. [DOI] [PubMed] [Google Scholar]
  • 69.Shimizu N, Hashidate H, Ota T, Suzuki T, Yatsunami M. Characteristics of intensity-based physical activity according to gait ability in people hospitalized with subacute stroke: a cross-sectional study. Phys Ther Res. 2019;22(1):17–25. 10.1298/ptr.e9971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Manns P, Ezeugwu V, Armijo-Olivo S, Vallance J, Healy GN. Accelerometer-derived pattern of sedentary and physical activity time in persons with mobility disability: National Health and Nutrition Examination Survey 2003 to 2006. J Am Geriatr Soc. 2015;63(7):1314–23. 10.1111/jgs.13490. [DOI] [PubMed] [Google Scholar]
  • 71.Ross R, Janssen I, Tremblay MS. Public health importance of light intensity physical activity. J Sport Health Sci. 2024;13(5):674–5. 10.1016/j.jshs.2024.01.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Lavie CJ, Lin GM, Ross R. Invited commentary: Health benefits associated with an active lifestyle in the elderly population: unique opportunities associated with light-intensity physical activity. Can J Cardiol. 2025;41(3):478–80. 10.1016/j.cjca.2024.07.017. [DOI] [PubMed] [Google Scholar]
  • 73.Newman AB, Simonsick EM, Naydeck BL, Boudreau RM, Kritchevsky SB, Nevitt MC, et al. Association of long-distance corridor walk performance with mortality, cardiovascular disease, mobility limitation, and disability. JAMA. 2006;295(17):2018–26. 10.1001/jama.295.17.2018. [DOI] [PubMed] [Google Scholar]
  • 74.Van Abellan G, Rolland Y, Andrieu S, Bauer J, Beauchet O, Bonnefoy M, et al. Gait speed at usual pace as a predictor of adverse outcomes in community-dwelling older people an International Academy on Nutrition and Aging (IANA) Task Force. J Nutr Health Aging. 2009;13(10):881–9. 10.1007/s12603-009-0246-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Brown DMY, Burkart S, Groves CI, Balbim GM, Pfledderer CD, Porter CD, et al. A systematic review of research reporting practices in observational studies examining associations between 24-h movement behaviors and indicators of health using compositional data analysis. J Act Sedentary Sleep Behav. 2024;3(1):23. 10.1186/s44167-024-00062-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Prince SA, Cardilli L, Reed JL, Saunders TJ, Kite C, Douillette K, 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]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

12966_2026_1939_MOESM1_ESM.docx (225.4KB, docx)

Additional file 1: Table A1. Boundary values between the low, moderate and high tertiles for each mobility measure. Table A2. Self-reported chronic conditions diagnosed by a doctor for chronic conditions variable. Table A3. Partial η² effect sizes of self-report and performance-based mobility measures in capturing waking-day movement behaviour composition. Figure A1. Results of power analysis.

Data Availability Statement

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.


Articles from The International Journal of Behavioral Nutrition and Physical Activity are provided here courtesy of BMC

RESOURCES