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Study identifier: NCT06461741 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

EMG Biofeedback Training to Improve Balance in Individuals with Multiple Sclerosis

Condition: Multiple Sclerosis  ·  Sponsor: McMaster University

PhaseNA
Planned participants46
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to test the impact of a novel dual-task EMG Biofeedback training method for improving balance in individuals living with multiple sclerosis. The main question\[s\] it aims to answer are: * Does dual-task EMG biofeedback training deliver lasting balance benefits up to 3 months following the intervention? * Are the benefits greater than those for participation in traditional balance training exercises? * Do the benefits vary with the severity of disability? Participants will receive either EMG Biofeedback (EMG-BF) training or traditional balance exercise (BAL-EX) training. Both treatments involve three 30-minute sessions of the training every week for 6 weeks (18 sessions). During the sessions, participants in the EMG-BF treatment group will perform targeted exercises using feedback from adhesive (sticker) sensors on their arms and legs. Participants in the BAL-EX treatment group will following an instructor through balance training movements that are traditionally prescribed by physiotherapists to improve balance. Measurements will be taken at the beginning of the study, after six weeks of training, and three months after the end of training. Researchers will compare the groups to see if balance and related outcomes are improved more by 6-weeks of EMG-BF training than BAL-EX.

This description comes directly from the study's public registry record.

Talk to the study team

Aimee J Nelson, PhD  ·  905 525 9140  ·  nelsonaj@mcmaster.ca

Stephen L Toepp, PhD  ·  2896964538  ·  toeppsl@mcmaster.ca

Always discuss trial participation with your own doctor first.

Locations (1)

McMaster UniversityHamilton, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06461741