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NCT05998616Terminated

Feasibility of Remote Exercise Training for Hispanics/Latinos With MS

The Feasibility and Efficacy of a Remotely Delivered Exercise Training Intervention for the Hispanic/Latino Community With Multiple Sclerosis

Source: ClinicalTrials.gov · Last updated 7 Aug 2026

Brief summary (registry, in English)

The goal of this clinical trial is to investigate the potential benefits of a specially designed exercise program for Hispanics/Latinos with multiple sclerosis (MS). The main questions it aims to answer are: * Can a 4-month remotely-delivered exercise training program improve physical function, symptom management, and quality of life in Hispanics/Latinos with MS? * How do social determinants of health, such as income, education, access to healthcare, and social support, influence the feasibility and effectiveness of the exercise intervention? Participants in this study will engage in a 4-month remotely-delivered exercise training intervention that includes flexibility, or aerobic and resistance exercise training sessions. They will work with experienced coaches who will guide and support them throughout the program. The researchers will compare the participants who receive the exercise intervention with a control group to see if the exercise program leads to significant improvements in physical function, fatigue, mood, and overall well-being for Hispanics/Latinos with MS. The study aims to empower this underserved population and provide insights for future healthcare and research initiatives.

Status (registry)
Terminated
Study type
Interventional
Enrollment
33 (actual)
First submitted
1 Aug 2023
Start date
27 Apr 2024
Primary completion date
30 Jun 2025
Lead sponsor
University of Illinois Chicago
NCT number
NCT05998616

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Not between 18-65 years
  • No diagnosis of MS
  • Not relapse-free for at least 30 days
  • Not able to walk with or without an assistive device
  • Too much physical activity (i.e. 150 minutes or more of moderate to vigorous physical activity per week)
  • Not willing to complete all required testing procedures, outcome questionnaires, and randomization
  • Do not identify as Hispanic/Latino
  • Unable to speak, read, and understand English
  • Not currently residing in Chicago
  • No access to the internet and email
  • Not safe for exercise based on the PAR-Q

Who the study is looking for

  • Age between 18-65 years
  • Diagnosis of MS
  • Relapse-free for at least 30 days
  • Able to walk with or without an assistive device
  • Insufficient physical activity (i.e., not meeting current physical activity guidelines of 150 minutes of moderate to vigorous physical activity per week)
  • Willingness to complete all required testing procedures, outcome questionnaires, and randomization
  • Identify as Hispanic/Latino
  • Able to speak, read, and understand English
  • Currently reside in Chicago
  • Access to the internet and email
  • Safe for exercise based on the Physical Activity Readiness Questionnaire (PAR-Q)

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Illinois at ChicagoChicagoUnited StatesUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.