Chandelier
Senior Member (Voting Rights)
Measurement properties of the 30-second sit-to-stand test in post COVID-19 condition: Results from the PYCNOVID randomised controlled trial
Data were collected at screening, at baseline (approximately 2 weeks after screening), and at follow-up (12 weeks after baseline).
Using screening and baseline data, agreement was evaluated using Bland-Altman analysis (mean bias and limits of agreement), alongside the intraclass correlation coefficient (ICC) and the minimal detectable change (MDC95).
Correlation coefficients were used to assess relationships between the 30s-STS test, physical activity, and key PCC-related symptoms.
The minimal important difference (MID) was estimated with data from baseline and at 12-weeks using anchor- and distribution-based methods.
The 30s-STS was safe (no adverse event) and feasible.
Overall, test performance was reduced, 46% of participants had z-score values below the 5th percentile.
The test showed good test-retest reliability (ICC 0.82 [95% CI, 0.76 to 0.86]) with no indication for a systematic learning effect; however, the limits of agreement were wide.
Mean bias between was 0.84 repetitions (95% CI, 0.26 to 1.42). The MDC95 was 4.25 repetitions.
Correlations with physical activity and key PCC-related symptoms were weak. Distribution-based methods yielded MID values between 1.38 and 3.23 repetitions.
Change correlations between 30s-STS repetitions and the anchors were insufficient for anchor-based MID calculation.
Changes exceeding four repetitions surpass measurement error (MDC95), while distribution-based estimates suggest a provisional MID of two repetitions.
Further studies are needed to establish a triangulated MID to better capture patient-relevant change.
Web | DOI | PMC | PDF | PLOS One | Open Access
Braun, Julia; Kopp, Julia; Künzi, Lisa; Puhan, Milo A; Fehr, Jan S; Radtke, Thomas
Abstract
Background
The 30-second sit-to-stand test (30s-STS) is a frequently used measure of functional capacity in post-COVID-19 condition (PCC), but its measurement properties have not been comprehensively investigated.Methods
We used data from the PYCNOVID randomised controlled trial to examine feasibility, safety, test-retest reliability, construct validity (correlations with key symptoms and physical activity), and responsiveness to change of the 30s-STS.Data were collected at screening, at baseline (approximately 2 weeks after screening), and at follow-up (12 weeks after baseline).
Using screening and baseline data, agreement was evaluated using Bland-Altman analysis (mean bias and limits of agreement), alongside the intraclass correlation coefficient (ICC) and the minimal detectable change (MDC95).
Correlation coefficients were used to assess relationships between the 30s-STS test, physical activity, and key PCC-related symptoms.
The minimal important difference (MID) was estimated with data from baseline and at 12-weeks using anchor- and distribution-based methods.
Results
Data from 150 adults with PCC (74.7% female) were analysed.The 30s-STS was safe (no adverse event) and feasible.
Overall, test performance was reduced, 46% of participants had z-score values below the 5th percentile.
The test showed good test-retest reliability (ICC 0.82 [95% CI, 0.76 to 0.86]) with no indication for a systematic learning effect; however, the limits of agreement were wide.
Mean bias between was 0.84 repetitions (95% CI, 0.26 to 1.42). The MDC95 was 4.25 repetitions.
Correlations with physical activity and key PCC-related symptoms were weak. Distribution-based methods yielded MID values between 1.38 and 3.23 repetitions.
Change correlations between 30s-STS repetitions and the anchors were insufficient for anchor-based MID calculation.
Conclusions
The 30s-STS test is feasible, safe, and demonstrates good test-retest reliability.Changes exceeding four repetitions surpass measurement error (MDC95), while distribution-based estimates suggest a provisional MID of two repetitions.
Further studies are needed to establish a triangulated MID to better capture patient-relevant change.
Web | DOI | PMC | PDF | PLOS One | Open Access