Home-based e-based exercise protocol feasibility study for patients with multiple sclerosis and comorbidities
The study design involves a feasibility study with 50 participants and a prospective randomized controlled trial (RCT) protocol planned for 300 participants. The population includes pwMS with and without comorbidities, receiving a home-based e-based physical exercise program supervised online by physiotherapists. The comparator is usual care. The intervention consists of resistance training with resistance bands targeting the lower extremities, delivered as two 60-minute sessions per week for 24 weeks.
Feasibility results indicate a recruitment rate of 91.3% (21 of 23 eligible participants enrolled). Follow-up completion was 76.2% (16 of 21 enrolled participants completed follow-up). Mean attendance was 15.2 sessions per participant, ranging from 6 to 22 sessions. The adherence rate was 63%. Two participants in the intervention group did not begin the program due to occupational constraints. No intervention-related adverse events were reported during the feasibility phase.
Primary efficacy outcomes, specifically changes in walking capacity using the 6-minutes' walk test, have not yet been reported as this publication is a protocol. Secondary outcomes include the NEDA-3 scale, quality of life measures, fatigue, and neurofilament light chain levels. Key limitations include the feasibility-only nature of current data and recruitment constraints related to occupational factors. Causality regarding the e-based exercise program's effect on outcomes is to be evaluated in the upcoming prospective RCT. Safety data is currently limited to adverse events observed during the feasibility study.