Multiple Sclerosis (MS) Clinical Trials

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Evaluation of the Effect of Quran Recitation on Fatigue and Mental Well-Being in MS Patients: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study will be conducted to evaluate the effects of Quran recital on fatigue and mental well-being in patients with multiple sclerosis. Hypotheses: 1. Quran recital reduces fatigue in MS patients. 2. Quran recital increases mental well-being in MS patients. The patients will be called by the researcher to ask whether they continue this practice. The control group will continue their routine treatment and care and no additional intervention will be applied. The final test measurements will be made by meeting with the patients in the hospital at the end of the 4th week.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Having been diagnosed with Multiple Sclerosis at least 6 months ago

• Being between the ages of 18-80

• Agreeing to participate in the research

• Not having any obstacles to wearing headphones

• Not having any hearing problems

Locations
Other Locations
Turkey
Van Yüzüncü Yıl University Dursun Odabaş Medical Center
RECRUITING
Van
Contact Information
Primary
SEVGİ DEMİR ÇAM, Asst. Prof
sevgidemir91@hotmail.com
905073468284
Backup
Yavuz Üren, Asst. Prof
yavuzuren@yyu.edu.tr
905065961050
Time Frame
Start Date: 2025-09-09
Estimated Completion Date: 2026-05-15
Participants
Target number of participants: 52
Treatments
Experimental: Experimental group
The Quran recital group will be asked to listen to the Quran (Surah Yasin) for half an hour with an mp3 player given to them between 21:00-22:00 3 days a week (Monday-Wednesday-Friday) and they will be asked to continue this practice for 4 weeks. The patients will be called by the researcher to ask whether they continue this practice. The final test measurements will be made at the end of the 4th week by interviewing the patients at the hospital.
No_intervention: Control group
Personal and contact information about the patients will be recorded and pre-test forms will be applied. The control group will continue their routine treatment and care and no additional intervention will be applied. Post-test measurements will be made by meeting with the patients at the hospital at the end of the 4th week.
Related Therapeutic Areas
Sponsors
Leads: Artvin Coruh University

This content was sourced from clinicaltrials.gov