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Effect of a 4-week pulmonary telerehabilitation program for people with respiratory post-acute sequelae of COVID-19 -- a randomised controlled trial
Reeves JM, Spencer LM, Tsai LL, Baillie AJ, Han Y, Leung RWM, Bishop J, Troy LK, Corte TJ, Teoh AKY, Peters M, Barton C, Jones L, Alison JA
European Journal of Physiotherapy 2025;27(6):402-411
clinical trial
This trial has not yet been rated.

PURPOSE: To evaluate a 4-week pulmonary telerehabilitation (PTR) program compared to usual care for people with persistent respiratory post-acute sequelae of COVID-19 (PASC). METHODS: A multi-centre randomised controlled trial with remote assessment and assessor blinding. Participants were randomised 1:1 to 4-weeks, twice-weekly PTR or usual care (Control Group (CG)). PTR exercise intensity was titrated based on fatigue and dyspnoea. After the control period, participants in CG could cross-over into PTR to form a combined group (PTR-X). PRIMARY OUTCOME: 1-minute sit-to-stand test (1-minSTST). SECONDARY OUTCOMES: 5-repetition sit-to-stand test; Montreal Cognitive Assessment blind-version; COVID-19 Yorkshire Rehabilitation Scale; COPD Assessment Test; 36-Item Short-Form Health Survey; Hospital Anxiety and Depression Scale; Fatigue Severity Scale; Kessler Psychological Distress Scale, all assessed at baseline and following intervention or control periods. Data were analysed using a linear mixed effects model. RESULTS: Of 50 participants recruited, 39 completed the study (PTR group n = 14, CG n = 25). There were no statistically significant between-group differences in any outcomes. For the PTR-X group (n = 27) there was a statistically significant within-group improvement in 1-minSTST (2.4 repetitions, 95% CI 0.6 to 4.2). CONCLUSIONS: A 4-week (8 session) PTR intervention for respiratory PASC showed no significant between-groups differences suggesting that longer PTR programs or alternative interventions should be evaluated.

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