1. Introduction
Submaximal field walking tests, such as the 6 min walk test (6MWT), are essential functional assessments to evaluate an individual’s capacity for daily activities and overall physical performance [
1,
2], by providing valuable insights into an individual’s endurance and functional capacity, particularly in clinical populations. Field walking tests are accessible, carry a lower risk than maximal tests [
3], and are particularly beneficial for older patients [
4] or those with heart failure or chronic respiratory diseases [
2]. While the 6MWT remains the gold standard for assessing mortality risk and prescribing exercise intensity, establishing normative data provides a vital comparative framework for clinical practice [
5]. Benchmarking walking test results against population norms enables clinicians to gauge the severity of a condition, tailor treatments, and enhance patient motivation and adherence. However, certain populations are unable to complete the 6MWT due to severe dyspnoea or fatigue, suggesting that the 3MWT may be a more feasible, time-efficient alternative.
The 3MWT correlates strongly with the 6MWT and is particularly useful for individuals with limitations that hinder completion of longer tests [
6]. Its reliability and clinical applicability make it an effective tool for assessing functional capacity in diverse populations, especially among the obese [
6], paediatric [
7], and geriatric [
8] populations, as well as those with respiratory conditions [
9]. Physiologically, short-duration walking tests may place greater emphasis on early acceleration, pacing and habitual walking velocity, whereas the 6MWT is better understood as a submaximal test that reflects integrated cardiopulmonary and musculoskeletal capacity [
2]. Consequently, the 3MWT is especially beneficial in clinical settings where time and patient tolerance are critical factors, providing a practical alternative to traditional walking tests.
Several studies from Belgium [
7], Turkey [
6], and Japan [
8] have derived normative reference values (NRV) and reference equations to estimate the 3MWT in their populations. Key determinants of performance include age and height [
7]. Yet these foreign models cannot be applied accurately to local contexts due to significant variations in sample characteristics and test methodologies; such differences have been shown consistently in the local context, such as in the case of 6MWT [
10], incremental shuttle walk [
11], and timed-up-and-go tests [
12]. Culturally, habitual physical activity levels and urban environments vary drastically between European and Asian cohorts. Anatomically, distinct anthropometric differences [
13], such as the characteristically shorter stature, directly alter step frequency and stride length, potentially influencing the total 3MWT distance. Furthermore, existing international studies exhibit vast methodological disparities; differences in corridor lengths [ranging from 20 to 50 metres (m)] [
1,
2] and varying pacing instructions (brisk versus self-paced) [
14] limit their comparative validity. Crucially, much of this surrounding literature remains limited by narrow age stratification that fails to capture full lifespan trajectories, a lack of standardisation regarding trial learning effects, and an unverified assumption of linear equivalence between 3 and 6 min test durations.
Beyond these geographical disparities, existing international reference equations for the 3MWT exhibit distinct structural limitations that restrict their broader clinical utility. Many historical cohorts were constrained to narrow, isolated age bands, predominantly paediatric or geriatric groups, thereby failing to capture the non-linear functional trajectories that span the full adult lifespan. Furthermore, previous studies frequently overlooked the confounding influence of systematic learning effects between successive trials. Critically, much of the surrounding literature operates on the unverified assumption of a uniform, linear relationship with the 6MWT, mathematically extrapolating data without empirically evaluating duration-dependent pacing dynamics or acute cardiorespiratory strain. These collective methodological gaps underscore the necessity of establishing robust, lifespan-spanning reference values using highly standardised, multi-trial protocols.
To date, no local studies have investigated the NRV for the 3MWT, leaving a significant gap in the objective assessment of functional exercise capacity within the Singaporean population. Relying on foreign benchmarks or existing local 6MWT equations compromises assessment accuracy, potentially leading to over- or underestimation of functional impairment. Establishing these values is crucial for clinical application. By addressing the lack of localised anthropometric and demographic data, this study provides a vital framework for more precise, culturally relevant interpretations of 3MWT performance.
Hence, this study aims to: (1) evaluate the NRV of the 3MWT in a healthy population, stratified by gender and age groups; (2) determine the univariate correlations of demographic, anthropometric and physiological variables that influence 3MWT performance; (3) establish 3MWT reference equations applicable to healthy adults using both pre- and post-test predictive variables; (4) evaluate the clinical utility of the 3MWT by comparing age-matched local data with established 6MWT reference values.
2. Materials and Methods
2.1. Study Design
This cross-sectional study utilised convenience sampling with a targeted age-and-gender stratification framework across six decades (21 to 80 years) to evaluate community-dwelling healthy adults. Participants were recruited via community outreach, public notices, and word-of-mouth across multiple regional districts in Singapore to enhance population representation. Data collection was conducted between March 2024 and November 2025. The University Institutional Review Board granted ethical approval (RECAS-0253 & RECAS-0514). All procedures were performed in accordance with local institutional guidelines and regulations.
All participants provided voluntary written informed consent before data collection. Data collection was conducted within university facilities by trained investigators proficient in administering the 3MWT and related functional assessments. All measurements for each participant were completed within a single session, with no further follow-up required.
2.2. Participants
2.2.1. Sample Size Estimation and Justification
The sample size was determined to ensure sufficient power to develop a robust 3MWT reference equation and establish the NRV across the adult lifespan. Using a stratified sampling strategy, we aimed to recruit at least 20 participants per gender per decade across six age strata (21 to 80 years), for an ideal total target of 240 participants. While this recruitment target was fully achieved in the younger cohorts, the final sample reflected a lower field with the older stratum due to strict exclusion criteria and participant sign-up response. Despite these subgroup variations, the final aggregate sample (N = 240) remains highly robust for the primary statistical modelling. An a priori power analysis using G*Power (v3.1.9.7) for multivariable linear regression indicated that with a medium effect size (f
2 = 0.15), α = 0.05 and up to 10 predictors, a sample of N = 118 is required to achieve a power of 0.95. The sample size (n = 240) comfortably exceeds the requirements, ensuring excellent model stability. The 10 independent variables were predefined based on clinical covariates known to influence walking distance (demographics, anthropometrics, and physiological responses). This satisfies the multivariable linear regression analysis (N ≥ 50 + 8
k, where
k is the number of predictors) [
15], maintaining a 24:1 participant-to-variable ratio to prevent overfitting. Additionally, the target of n = 20 per gender cell (n = 40 per decade) provides adequate statistical precision to construct stable 95% confidence intervals for population norms, given a previously reported median 3MWT of 316 metres [Interquartile range (IQR) 282.5 to 336.8] [
16]. This sample size provides sufficient precision to establish reliable clinical equations for the local population.
2.2.2. Inclusion and Exclusion Criteria
The Physical Activity Readiness Questionnaire for Everyone+ (PAR-Q+) first screened healthy adults [
17], with the following inclusion criteria: (1) community-dwelling adults aged 20 to 80 years; (2) Body mass index (BMI) < 27.5 kg/m
2 [
18]; (3) ability to walk independently for three minutes without the use of walking aids; (4) proficiency in English to comprehend test instructions. Health status and medical history, including current medication use, were evaluated via this standardised self-report screening tool. Participants were excluded if they: (1) indicated “Yes” to any medical follow-up questions on the PAR-Q+, which included screening for regular prescription medications for chronic diseases; (2) presented with abnormal resting haemodynamic, defined as systolic blood pressure (SBP) ≤ 90 mmHg or ≥140 mmHg, and/or diastolic blood pressure (DBP) ≤ 60 mmHg or ≥80 mmHg; (3) reported any uncontrolled cardiovascular, neuromuscular, musculoskeletal, or metabolic conditions that could impair functional exercise capacity; (4) reported a fever or temporary illness within the past 24 h before testing. The BMI threshold of <27.5 kg/m
2 was deliberately chosen in accordance with the World Health Organisation (WHO) guidelines for the Asian population, which define a BMI ≥ 27.5 kg/m
2 as clinical obesity. Given that obesity is classified as a chronic metabolic disease by the WHO, this cut-off was essential to isolate the genuinely healthy, non-obese cohort, ensuring the derived reference values represent true normative physiological capacity. Furthermore, the resting BP cut-off aligns with contemporary international hypertension guidelines [
19], thereby excluding individuals with early-stage, undiagnosed cardiovascular disease. Although the protocol allowed exclusion if data collection was terminated due to adverse reactions during the 3MWT, no participants were excluded during the study period.
2.3. 3-Min Walk Test (3MWT)
The 3MWT was conducted in accordance with established 6 min walk test guidelines [
1,
2], and adapted for a 3 min duration [
16,
19]. The test took place on a sheltered, 30 m straight walkway marked with cones at the 0 and 30 m points. Chairs were positioned at both ends and at the 15 m midpoint for participant safety and rest. Participants rested in a seated position for at least 5 min before the trial. Baseline measurements, including blood pressure (BP), pulse rate (PR), and oxygen saturation (SpO
2) via pulse oximetry, were recorded. The Borg Rating of Perceived Exertion scale (RPE) [
20] was explained, and initial resting scores were obtained.
The following standardised instructions were provided to all participants:
“The objective of this test is to walk as far as possible for 3 min. You will walk back and forth in this walkway. You are permitted to slow down, stop, and rest as necessary; you may sit down, but should resume walking as soon as you can. You should pivot briskly around the cones and continue back the other way without hesitation. Remember that the goal of this test is to walk as far as possible for 3 min, but do not run or jog.”
Standardised verbal encouragement was provided at 30 s intervals, using the phrases “You are doing well” and “keep up the good work” alternately. At the 2 min and 45 s mark, a final reminder of the remaining time was given to maintain consistent motivation. At the end of the test, participants were asked to stand where they stopped, and a chair was brought to them so that they could sit and rest. Two trials were administered to account for the learning effect, separated by a minimum 15 min rest period. To ensure complete physiological recovery between trials, particularly for older or less conditioned adults, the initiation of the second trial was strictly conditional upon the participant’s vital signs (heart rate and blood pressure) returning to within ±10% of their baseline resting values, alongside a subjective return to a resting Borg RPE score. An additional rest extension was provided upon request to ensure that vital signs returned to baseline before the second trial. The total distance was recorded in metres (m). For all data analyses, the greater distance achieved between the two trials (the best distance) was used.
2.4. Data Collection
Participants were instructed to attend the session in comfortable clothing and appropriate walking shoes. Before data collection, participants provided physical profiles, including PAR-Q+, anthropometric measurements, height (m) and weight [kilograms (kg)], with BMI calculated using the standard formula: BMI = weight (kg)/height (m)
2. Resting haemodynamic parameters, including BP, PR, and SpO
2, were measured using an Omron
® portable blood pressure monitor (EZ | HEM-7183) (Omron, Kyoto, Japan) and a Nellcor
® pulse oximeter (PM10N) (Nellcor, Hayward, CA, USA). To assess the physiological intensity of the test, the following cardiovascular variables were derived: Predicted Maximum HR (HRmax) calculated using HRmax = 208 − (0.7 × Age) [
21]; while the HR Reserve (HRR) was calculated as the difference between HRmax and the resting HR (HRrest): HRR = HRmax − HRrest. Additionally, Percentage of Predicted Maximum Heart Rate (%predHRmax) = (Highest HR during 3MWT/HRmax) × 100%. Perceived exertion was assessed with the RPE scale [
20]. To ensure validity, the scale was explained using the repeat-back method, confirming each participant’s understanding of the scoring system before recording pre- and post-test RPE values.
2.5. Pilot Trial and Reliability
A pilot trial (n = 30) was conducted using the main study’s eligibility criteria to familiarise the team with the protocol and evaluate the intra- and inter-rater reliability of the 3MWT. To assess reliability, each pilot participant underwent three 3MWT trials. Data was collected concurrently and independently by the investigators. Since the operational protocol, testing environment, and eligibility criteria were identical to those of the main study, these 30 participants were pooled in the final analysis to maximise statistical power. To ensure full methodological consistency with the full-scale cohort, only the first two trials from the pilot participants were utilised to extract the optimal walking distance for the primary analysis.
2.6. Full-Scale Study
Following the successful completion of the pilot phase, the full-scale study was initiated using the identical inclusion and exclusion criteria. All participants completed two trials of the 3MWT. For all 240 participants across both phases, the longest distance achieved between the first two standardised trials was taken as the primary outcome measure.
2.7. Statistical Analysis
Statistical analysis was performed using GraphPad Prism Version 8.4.3, with a significance level of
p < 0.05. Data normality was assessed using the Shapiro–Wilk test. Descriptive statistics included the mean and standard deviation (SD), median and IQR, and 95% confidence interval (95% CI) for the median. Differences between genders were analysed using the Mann–Whitney U test, with the Point-Biserial correlation (r) as the effect size, while the Kruskal–Wallis test evaluated differences across age groups. The strength of
r was categorised as very weak (0.00 to 0.19), weak (0.20 to 0.39), moderate (0.40 to 0.59), strong (0.60 to 0.79) or very strong (0.80 to 1.00). Intra- and inter-rater reliability were evaluated using two-way mixed-effects, absolute agreement, and single-measure intraclass correlation coefficients (ICC). To ensure objectivity during reliability testing, distance measurements were standardised using a pre-marked corridor and measurement wheel rounded strictly to the nearest 0.1 metre. ICC values were interpreted as follows: <0.50 indicated poor reliability; 0.50–0.75, moderate reliability; 0.75–0.90, good reliability; and >0.90, excellent reliability [
22]. Spearman’s correlation coefficient (ρ) determined the strength of the relationship between 3MWT and independent variables. The strength of the correlation (ρ) was interpreted as follows: negligible (<0.30), low (0.30–0.49), moderate (0.50–0.69), high (0.70–0.89), and very high (≥0.90) [
23]. Multiple linear regression analysis with a forward stepwise selection method was used to develop reference equations for the 3MWT based on pre- and post-test variables. Before final model acceptance, the regression assumptions of linearity and normality of the residuals were verified by inspecting residual plots. To avoid multicollinearity, independent variables with high conceptual and mathematical redundancy were restricted from entering the same model. To compare the measured 3MWT against two predicted distances derived from established reference equations [
13,
14], the Friedman test was employed, followed by Dunn’s post hoc test with Bonferroni adjustment to account for multiple comparisons and maintain the family-wise error rate at
p < 0.05.
3. Results
Figure 1 illustrates the participant recruitment and flow. Of the 246 participants screened, six were excluded, resulting in a final sample of 240 (males: n = 114, 47.5%; females: n = 126, 52.5%). The cohort included the pilot trial (n = 30, 12.5%) and the full trial phase (n = 210, 87.5%). There was no missing data due to the prospective study design. Detailed demographic and anthropometric characteristics are summarised in
Table 1. The median age of all participants was 35.5 years (IQR 24.0 to 54.0), with an overall age range of 20 to 80 years. The 3MWT is reported as 290.0 m (IQR 257.0 to 323.0) [female: 282.0 (IQR 255.0 to 314.0); male: 302.0 (IQR 264.0 to 332.0);
p = 0.002; r = 0.170]. The difference between Trials 2 and 1 is 7.0 m (IQR 0.0 to 16.0), which is approximately 2.4% of the difference between the two trials. Notably, the %predHRmax is only 38.3 (IQR 0.0 to 48.3) among these healthy participants.
Figure 2 and
Figure 3 depict the age-stratified 3MWT for female and male participants, respectively. Significant age-related differences in the 3MWT were observed in female participants (
p = 0.005), with post hoc analysis showing a progressive decline in distance with increasing age. In contrast, male participants showed no significant differences in walk performance across the 20-to-80-year age span (
p = 0.225), a trend also evident in the analysis of the total cohort, which showed no statistically significant differences across the age decades (
p = 0.397). The 3MWT showed high intra-rater reliability (ICC = 0.921, IQR: 0.861–0.959) and perfect inter-rater reliability (ICC = 1.0, IQR: 1.000–1.000), reflecting total agreement between assessors.
Table 2 presents variables that are correlated with the 3MWT. Among all pre-test variables, age, height, and resting PR are the only ones that correlate with the 3MWT. At the same time, the net changes in BP, PR, SpO
2, and RPE, together with %predHRmax, are the post-test variables that correlate.
Table 3 and
Table 4 present the multiple linear regression models for the determinants of 3MWT. The baseline model, including only pre-test variables, explains 16% of the variance (R
2 = 0.16,
p < 0.001). Predictive power improved significantly to 47% (R
2 = 0.47,
p < 0.001) when post-test physiological responses were included, identifying age and changes in SBP, PR, and RPE as the primary drivers. This marked increase in explained variance indicates that incorporating post-test physiological variables and perceived exertion scores substantially improves the model’s explanatory power compared to utilising baseline demographics alone.
The evaluation of the relationship between the 3MWT and established 6 min walk distance benchmarks reveals that the median of the 2 × 3MWT was 579.0 metres (514.0 to 645.0). This is significantly higher than the predicted 6 min walk distance calculated using the Poh et al. (2006) [
24] [442.0 metres (IQR 354.0 to 542.0)] and Yeung et al. (2022) [
10] [436.0 metres (IQR 313.0 to 480.0)] equations (
Table 5). Friedman’s test showed a statistically significant difference across these measures (
p < 0.001; adj
p < 0.001). These results suggest that participants maintained a higher average speed during the 3 min walk test than would be predicted for a 6 min duration.
4. Discussion
To our knowledge, this is among the first studies to establish normative reference values (NRV) for the 3MWT in healthy adults spanning the full adult lifespan. While the 6MWT is the clinical gold standard [
2], the 3MWT is a time-efficient alternative for busy settings or patients with limited endurance [
19]. However, compared to the 6MWT, there remains a significant lack of comprehensive reference data and validated equations for the 3 min format. The study’s overall median 3MWT, 290.0 m (IQR 257.0 to 323.0), for participants aged 20 to 80 years, aligns closely with recent findings from Japan [
8]. However, a more granular analysis reveals distinct age-related trends between genders. Among younger cohorts, the mean distances for females (314.8 ± 46.4 m) and males (343.3 ± 33.2 m) were slightly higher than our age-matched medians, 301.7 m (IQR 274.0 to 321.3) and 315.0 m (IQR 278.5 to 358.8), respectively. Interestingly, this performance gap appears to narrow or reverse in the older cohort (ages 70 to 80). While it was significantly lower for males (280.5 ± 44.9 m) and females (268.9 ± 24.9 m) among the Japanese participants, our cohort mostly maintained the distances, with medians of 276.9 m (IQR 218.0 to 313.8) and 270.2 m (IQR 255.5 to 283.1), respectively. These differences may stem from variations in the lifestyles, habitual occupational physical demands, or built-environment behaviours of the different populations. Furthermore, the normative values established in this study are generally higher than those reported in the obese populations [
6], a predictable finding given our BMI exclusion criteria, although BMI was not a correlating variable in this study. Conversely, our distances are lower than those reported by Yeung et al. (2025) [
16]. However, this difference is directly attributable to the earlier trial’s study design, which capped participation at age 64, thereby excluding the natural decline in walking performance observed in the seventh and eighth decades. Additionally, while earlier literature suggests the brief 3MWT format is highly applicable in specialised populations, care must be taken not to over-generalise early paediatric data, which has historically been limited to restricted cohorts of very young children [
7].
Univariate analysis identified age, gender, height, and resting PR as significant pre-test influences on 3MWT results. However, multiple linear regression revealed that age and resting PR were the only robust pre-test predictors, whereas age, changes in SBP, PR, and RPE dominated the post-test models. Notably, the median %predHRmax during the 3MWT was only 38.3%, lower than the greater cardiovascular strain typically observed during a standard 6MWT. This lower acute cardiovascular load indicates that a 3 min walking duration may not fully challenge the aerobic maximum of healthy, community-dwelling adults. Instead, performance over this shorter duration may better reflect self-selected habitual walking speed and pacing strategy. This physiological profile helps contextually reconcile the apparent discrepancy between our statistical models in male participants. Specifically, the group-level analysis showed no significant differences in 3MWT results across individual male age decades (p = 0.225) or across the total cohort (p = 0.397). This flat cross-sectional trajectory within the male subgroups is likely a statistical artefact due to insufficient localised statistical power, particularly in the heavily screened 70–80-year-old male cell (n = 5). When evaluated as a continuous variable across the entire aggregate lifespan sample (N = 240), the superior statistical weight of the whole-cohort linear regression model successfully identifies age as a highly significant, negative determinant (β = −0.7, p < 0.001), demonstrating that functional capacity does decline progressively over the lifespan when modelled continuously.
Our results demonstrate that mathematically doubling the 3MWT significantly overestimated 6 min capacity (from 514.0 to 645.0 m), highlighting a fundamental pacing discrepancy and that exertional fatigue accumulates non-linearly over time. Participants performing the shorter 3MWT appear to adopt a more aggressive, self-regulated pacing strategy that cannot be sustained for 6 min. Consequently, these preliminary comparative findings strongly indicate that a simple doubling of the 3MWT results is methodologically inappropriate for estimating equation-predicted 6MWT benchmarks, and the two tests should not be considered interchangeable without direct, concurrent validation.
Raw data show a clear divergence between functional walking performance and the underlying physiological effort required to maintain it across age strata. While absolute 3MWT metrics appeared relatively stable across certain age groups in the categorical analysis, a clear upward trend in %predHRmax indicates that older adults require a higher relative cardiovascular effort to achieve comparable walking distances. This increased cardiorespiratory demand is accompanied by a slower post-exercise heart rate recovery profile, indicating diminished cardiovascular deceleration in the older cohorts. This exertional gap is further reflected in our subjective findings: older participants reported greater increases in perceived exertion (RPE) during recovery intervals following test cessation. Taken together, these trends indicate that although older healthy adults possess the functional capacity to sustain a competitive walking velocity for a brief 3 min period, they do so at a significantly higher physiological cost, incurring a greater relative cardiorespiratory load and requiring a longer recovery period than their younger peers.
Limitations
Several limitations warrant consideration. First, the use of single-centre convenience sampling limits the generalisability and overall representativeness of the population. Strict health screening led to a lower yield in the oldest cohort (males: n = 5; females: n = 8, aged 71–80), reducing categorical subgroup power. However, for continuous multivariable regression, our aggregated sample (N = 240) is highly robust, more than doubling the minimum size (N = 118) required by an a priori power analysis (f2 = 0.15, α = 0.05, power = 0.95) to ensure model stability across the lifespan. Second, because the reference equations were developed and evaluated within the same sample, without external or internal validation (e.g., bootstrapping), they must be applied with clinical caution until independent validation is conducted. Additionally, while our rigid distance-verification protocol yielded perfect inter-rater reliability, this level of agreement is uncommon in wider clinical practice and should be interpreted with caution as a reflection of procedural standardisation rather than typical clinical variance. Thirdly, several primary determinants of functional capacity were not controlled for. Most notably, habitual physical activity levels, baseline fitness levels, specific medication use histories and socioeconomic status were not assessed, which limits the value of the reference norms. Additionally, peripheral lower-limb muscle strength and biomechanical variables were not measured, preventing us from isolating musculoskeletal versus cardiorespiratory contributions to the final 3MWT. Furthermore, although the protocol utilised two distinct walks, a potential trial-to-trial learning effect between consecutive efforts cannot be entirely ruled out. Finally, the strict inclusion filters, requiring English proficiency and excluding individuals with obesity, comorbidities, or ambulation with aids, particularly among the older cohorts, restrict participant recruitment, thereby limiting the generalisability of these reference values to other populations. Furthermore, because the 6MWT was not directly measured in this cohort, comparisons remain limited to equation-predicted benchmarks; prospective trials utilising concurrent testing and Bland–Altman analyses are required to confirm clinical interchangeability.