Actively Recruiting
Examining the Effects of a Remotely-delivered, Racially-tailored Exercise Training Program for Immediate and Sustained Improvements in Walking Dysfunction, Symptoms, and Health-related Quality of Life (HRQOL) Among African-Americans With Multiple Sclerosis (MS) Residing in Rural Environments.
Led by University of Illinois at Chicago · Updated on 2025-09-22
100
Participants Needed
1
Research Sites
204 weeks
Total Duration
On this page
Sponsors
U
University of Illinois at Chicago
Lead Sponsor
U
University of Alabama at Birmingham
Collaborating Sponsor
AI-Summary
What this Trial Is About
The proposed project involves a high-quality randomized controlled (RCT) design that examines the effects of a remotely-delivered, racially-tailored exercise training program for immediate and sustained improvement in walking dysfunction, symptoms, and health-related quality of life (HRQOL) among African-Americans with MS residing in rural environments. The primary analysis will test the hypothesis that those who are randomly assigned into the intervention condition (i.e., exercise training) will demonstrate (a) improvements in outcomes from baseline that (b) are sustained over 4-months of follow-up compared with those in the control condition (i.e., stretching).
CONDITIONS
Official Title
Examining the Effects of a Remotely-delivered, Racially-tailored Exercise Training Program for Immediate and Sustained Improvements in Walking Dysfunction, Symptoms, and Health-related Quality of Life (HRQOL) Among African-Americans With Multiple Sclerosis (MS) Residing in Rural Environments.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English as primary language
- Identify as African-American or Black
- Age of 18 years or older
- Diagnosis of MS
- Relapse free in the past 30 days
- Internet and email access
- Willingness to complete the outcome questionnaires
- Willingness to undergo randomization
- Insufficient physical activity (not meeting current physical activity guidelines based on GLTEQ)
- Mild-moderate ambulatory disability (MSWS-12 score between 25-49 & PDDS score between 2-4)
You will not qualify if you...
- Individuals not meeting the above inclusion criteria
- Individuals with moderate to high risk for contraindications of possible injury or death when undertaking strenuous or maximal exercise (PARQ)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Illinois at Chicago
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
R
Robert W Motl, PhD
CONTACT
E
Edson Flores, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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