The Effect of Remotely Delivered Pilates on Physical , and Psychological Outcomes in Individuals With Multiple Sclerosis
- Sponsor
- University of Illinois at Chicago
- Study ID
- NCT07504120
- Status
- Not Yet Recruiting
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Conditions
- Balance
- Cognition
- Depression
- Fatigue
- Fatigue in Multiple Sclerosis
- Multiple Sclerosis
- Pain Management
- Pilates Exercise
- Quality of Life
- Walking
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Pilates — BEHAVIORALREMOTLY PILATES EXERCISE
Study Details
Objectives Objective 1: To determine the effects of a 16-week remotely delivered Pilates intervention on walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS. Objective 2: To examine the impact of a 16-week remotely delivered Pilates intervention on depression \& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS. Aim Aim 1: To assess whether the 16-week remotely delivered Pilates intervention significantly improves walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS Aim 2: To investigate whether the 16-week remotely delivered Pilates intervention significantly improves depression \& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS. Hypothesis Hypothesis 1: The 16-week remotely delivered Pilates intervention will significantly improve walking endurance, walking speed, balance, fatigue, and pain compared to a waitlist control group in individuals with MS. Hypothesis 2: Participants receiving the 16-week remotely delivered Pilates intervention will demonstrate significantly greater improvements in depression \& anxiety, cognitive function, and QOL compared to a waitlist control group in individuals with MS.
Key Dates
- First listed
- Mar 31, 2026
- Start date
- Jun 1, 2026
- Status verified
- Aug 2025
- Primary completion
- Nov 1, 2027
- Completion
- Dec 1, 2027
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Other: Pilates groupBehavioral: Pilates group
- No Intervention: Control groupWaitlist Group
Primary Outcome Measure
Change from baseline in walking endurance (Six-Minute Walk Test distance) [ Time Frame: Baseline and 16 weeks (end of treatment) ]
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