Multiple Sclerosis (MS) Clinical Trials

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Effect of Multimodal Exercise Training on Disease Activity and Functional Status in Patients With Multiple Sclerosis

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The study aims to examine the effects of multimodal exercise training including aerobic, strengthening and balance exercises via face-to-face and asynchronous video-based telerehabilitation on disease activity, disability level, aerobic capacity, physical activity level, balance, fatigue level and quality of life in individuals with multiple sclerosis. Therefore, this study consists of two hypotheses. Hypotheses: H0: Multimodal exercise training has no effect on disease activity and functional status in patients with multiple sclerosis H1: Multimodal exercise training has effects on disease activity and functional status in patients with multiple sclerosis

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 65
Healthy Volunteers: f
View:

• Being diagnosed with multiple sclerosis by a neurologist

• Volunteering to participate in the study

• Being ambulatory

• EDSS between 3.0-5.5

• Being literate

• Having internet access

• Not having participated in a standardized physiotherapy and rehabilitation program in the last 3 months

Locations
Other Locations
Turkey
Istanbul University-Cerrahpasa
NOT_YET_RECRUITING
Istanbul
Istanbul University-Cerrahpasa
RECRUITING
Istanbul
Contact Information
Primary
Pelin Vural, MSc
pelinvural7@gmail.com
+905344245350
Time Frame
Start Date: 2025-02-10
Estimated Completion Date: 2028-05-01
Participants
Target number of participants: 40
Treatments
Experimental: Multimodal Exercise Training Group
Participants in the multimodal exercise training group will be given a treatment protocol consisting of aerobic exercise and strengthening exercises in the presence of a physiotherapist for a total of 12 weeks, 3 days a week for 1 hour.
Other: Control Group
Participants in the control group will be put on the waiting list after all assessment methods have been applied and will be re-evaluated at the end of 12 weeks.
Related Therapeutic Areas
Sponsors
Leads: Istanbul University - Cerrahpasa

This content was sourced from clinicaltrials.gov