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Study identifier: NCT06341023 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Functional Balance Intervention in Multiple Sclerosis

Condition: Multiple Sclerosis  ·  Sponsor: University of Illinois at Chicago

PhaseNA
Planned participants120
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

This project involves two sub-parts: Study 1: Effect of lab-based Functional Balance Intervention (FBI) for physical and cognitive symptoms of Multiple Sclerosis. Study 2: Feasibility of home-based FBI for physical and cognitive symptoms of Multiple Sclerosis. Each study involves a 2-arm, Phase-1, randomized controlled clinical trial to evaluate the effect of FBI on physical, cognitive function, and daily living among people with MS (PwMS). Study 1 is conducted in a lab setting, while Study 2 is conducted at home with additional safety measures. A total of 150 people with multiple sclerosis will be recruited and telephone screened, with an expected enrollment of 120 (60 per phase). After in-person screening, 96 eligible participants (48 per phase) will undergo pre-training assessment and randomization into FBI or Stretching groups. Training sessions will occur twice a week for four months. Anticipating a 15-17% attrition rate, the target sample size is 80 (40 per phase) for completion of the study. Post-training assessments will be conducted after four months to evaluate FBI's impact on physical and cognitive functions. This evidence-based protocol, previously successful with neurological and older adult populations, intends to provide a low-cost, safe, and effective intervention for PwMS in clinical and community settings, including rural areas.

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

Talk to the study team

Rudri Purohit, MS  ·  312-413-9772  ·  rpuroh2@uic.edu

Swaranka Deshmukh, MS  ·  3123553988  ·  sdeshm9@uic.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Illinois at ChicagoChicago, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06341023