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Home-based e-based exercise protocol feasibility study for patients with multiple sclerosis and comorbidities

Home-based e-based exercise protocol feasibility study for patients with multiple sclerosis and como…
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Key Takeaway
Note that primary efficacy outcomes are pending as this is a feasibility protocol for a future RCT.

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.

Study Details

Study typeRct
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
BackgroundComorbidity is prevalent among people with multiple sclerosis (pwMS) and may contribute to disease progression. Physical exercise (PE) reduces symptoms in pwMS and also benefits comorbidities. Digital (e)-based PE has been proposed as a tool to support the integration of PE.AimsTo describe a protocol for a randomized controlled trial (RCT) based on a structured approach and the results from a controlled feasibility study of an e-based PE intervention in pwMS with and without comorbidities.MethodIn a RCT following a feasibility study (n=50), patients will be randomly assigned in a 1:1 ratio to receive either usual care (n=150) or usual care plus an e-based PE program at home (n=150). The exercise program consists of resistance training with resistance bands targeting the lower extremities. The sessions will enable participants to engage in group exercises from their homes, supervised online by physiotherapists, two 60-minute sessions per week for 6 months (24 weeks and 48 sessions). The primary endpoint is change of walking capacity using the 6-minutes’ walk test. Secondary endpoints include “no evidence of disease activity” (NEDA)-3 scale, measures of quality of life and fatigue as well as levels of neurofilament light chain in blood and cerebrospinal fluid.Results of the feasibility study: Fifty individuals were eligible and randomized to an intervention group (n = 23) or to a usual care control group (n = 27). A total of 24 sessions were conducted for three months in groups of 6, supervised by the physiotherapist. In the intervention group, two pwMS did not begin the PE program due to occupational constraints with a resulting recruitment rate of 91.3% (21/23). Of the remaining 21 individuals, 16 (76.2%) completed the follow-up assessments with a mean attendance of 15.2 (range 6-22) sessions per participant, corresponding to a 63% adherence rate. No intervention‐related adverse events were reported.ConclusionThis protocol describes a prospective RCT study and the supporting feasibility data of an e-based PE performed at home. The effects of e-based PE performed at home will be evaluated, offering a significant contribution to the field of digital healthcare solutions and MS.Clinical Trial Registrationhttps://clinicaltrials.gov/, identifier NCT06298201.
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