Resistance Exercise Therapy After COVID-19 Infection: a Randomized, Controlled Trial
Abstract Body (Do not enter title and authors here): Objective:To determine the effects of a resistance exercise intervention on exercise capacity in adults after COVID-19 infection. Secondary objectives included assessments of health status.
Study Design: A two-arm randomized, controlled clinical trial including adults with a hospital or community diagnosis of COVID-19 in the preceding 12 months was undertaken during June 2021-April 2024. Population Studied: 233 individuals with persisting physical symptoms post-COVID-19. Intervention:Personalized resistance exercise intervention for 3-months. A guideline was provided by research staff supported by an exercise physiologist. The document included an exercise log and links to training videos. Control: Treatment-as-usual. Power Calculation:Taking a clinically important between-group difference in the incremental shuttle walk test (ISWT) at follow-up (3-months) to be 46 m, with a SD of 105m, the sample size providing 80% power, at 5% significance, with no loss to follow-up (LTFU) was 85 per group; allowing for LTFU, the target was 110 per group (220 total). Primary End Point:Distance achieved (m) in the ISWT at 3-months. Secondary End Points:Health-related quality of life (EQ-5D-5L), anxiety and depression (Patient Health Questionnaire) and grip strength (kg). Outcome:233 adults (median (interquartile range) 53.6 (43.8, 60.8) years; 146 (62.7%) female, 91 (39.1%) hospitalized with COVID-19 were randomized (n=117 (50.2%) intervention, n=116 (49.8%) control). The median (interquartile range) % adherence with the exercise intervention was 71.0 (47.8, 96.8), equivalent of performing exercises on 5 days/week. The mean (SD) distances achieved in the ISWT at baseline and at 3-months follow-up were 328 (225) m and 389 (249) m, in 224 and 193 individuals, respectively. The change in ISWT at 3-months compared to baseline was 83 (118) m in the intervention group (n=94) and 47 (95) m in the control group (n=98) (effect estimate (95%) confidence interval 36.5 (6.6, 66.3) m; p=0.017). Greater improvements in the intervention group were observed for the EQ-5D-5L utility score (0.06 (0.01, 0.11); p=0.018), Patient Health Questionnaire (0.5 (0.2, 0.8); p=0.013) and handgrip strength (2.58 (0.92, 4.24) kg; p=0.002). The cost of the intervention per participant was $252.
Conclusion: In this randomized clinical trial, a program of resistance exercise for 3 months in adults after COVID-19 infection, improved exercise capacity, quality of life, anxiety and depression, and grip strength.
Berry, Colin
( University of Glasgow
, Glasgow
, United Kingdom
)
Welsh, Paul
( UNIVERSITY OF GLASGOW
, Glasgow
, United Kingdom
)
Dawkes, Susan
( Edinburgh Napier University
, Edinburgh
, United Kingdom
)
Mcconnachie, Alex
( University of Glasgow
, Glasgow
, United Kingdom
)
Gray, Stuart
( University of Glasgow
, Glasgow
, United Kingdom
)
Mckinley, Gemma
( University of Glasgow
, Glasgow
, Lanarkshire
, United Kingdom
)
Bayes, Hannah
( NHS Greater Glasgow and Clyde Health Board
, Glasgow
, Lanarkshire
, United Kingdom
)
Anderson, David
( NHS Greater Glasgow and Clyde Health Board
, Glasgow
, Lanarkshire
, United Kingdom
)
Lang, Chim
( University of Dundee
, Dundee
, United Kingdom
)
Gill, Adam
( NHS Greater Glasgow and Clyde Health Board
, Glasgow
, United Kingdom
)
Sykes, Robert
( University of Glasgow
, Glasgow
, United Kingdom
)
Taggart, Diann
( NHS Greater Glasgow and Clyde Health Board
, Glasgow
, United Kingdom
)
Kamdar, Anna
( University of Glasgow
, Glasgow
, United Kingdom
)
Author Disclosures:
Colin Berry:DO have relevant financial relationships
;
Research Funding (PI or named investigator):Abbott:Active (exists now)
; Research Funding (PI or named investigator):Zoll Medical:Active (exists now)
; Research Funding (PI or named investigator):Xylocor :Active (exists now)
; Advisor:Novartis:Past (completed)
; Advisor:Servier:Past (completed)
; Advisor:Merck:Active (exists now)
; Advisor:Edwards LifeSciences:Active (exists now)
; Researcher:CorFlow:Active (exists now)
; Research Funding (PI or named investigator):Boehringer Ingelheim:Active (exists now)
; Research Funding (PI or named investigator):AstraZeneca:Past (completed)
; Advisor:AskBio:Active (exists now)
| Paul Welsh:No Answer
| Susan Dawkes:DO NOT have relevant financial relationships
| Alex McConnachie:DO NOT have relevant financial relationships
| Stuart Gray:DO NOT have relevant financial relationships
| Gemma McKinley:DO NOT have relevant financial relationships
| Hannah Bayes:No Answer
| David Anderson:No Answer
| Chim Lang:DO NOT have relevant financial relationships
| Adam Gill:DO NOT have relevant financial relationships
| Robert Sykes:DO have relevant financial relationships
;
Independent Contractor:Novartis:Past (completed)
; Research Funding (PI or named investigator):Medical Research Council:Active (exists now)
| Diann Taggart:DO NOT have relevant financial relationships
| Anna Kamdar:DO NOT have relevant financial relationships