Strength Training Exercises to minimise late Effects of childhood Leukaemia or lymphoma among adolescents (The STEEL study): protocol for a national multicentre randomised controlled trial
Riel, H.; Kristiansen, M. V.; Albertsen, B. K.; Fridh, M. K.; Jensen, C. F.; Larsen, H. B.; Rathe, M.; Svilshave, S.; Tuckuviene, R.; Vad, C.; Wiskemann, J.; Madeleine, P.
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BackgroundAdolescent cancer survivors (ACS) often experience long-term impairments in muscle strength, physical function, and quality of life. Strength training may help address these deficits, but there is limited evidence from randomised trials. This study investigates the efficacy of progressive strength training compared to low-load circuit training in increasing muscle strength over 16 weeks among ACS. MethodsIn this multicentre randomised controlled trial, we will recruit 60 ACS successfully treated for acute lymphoblastic leukaemia or lymphoma. Participants aged 10-19 years are recruited from paediatric oncology departments across Denmark. They are randomised stratified by sex to either: 1. a 16-week partly supervised progressive strength training programme (STEEL) with individually tailored exercises targeting major muscle groups, progressing in load and volume over time; or 2. a 16-week partly supervised circuit training programme involving aerobic and low-load strength exercises. The primary outcomes are the change in isometric muscle strength in elbow flexion and extension, and knee flexion and extension from baseline to the 16-week follow-up. Secondary outcomes include physical function (dynamic strength, rate of force development, grip strength, and walking endurance), health-related quality of life, metabolic markers, bone mineral density, movement-evoked pain, exercise compliance and fidelity, physical activity level, and participant satisfaction. DiscussionThis trial addresses the need for evidence-based rehabilitation strategies in ACS. It is designed to detect short-term effects of supervised strength training on key physical health outcomes using a robust, blinded, and clinically relevant comparison. Results may inform future survivorship care and guidelines. Trial RegistrationClinicalTrials.gov identifier: NCT05673152. Registered January 4, 2023.
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