Fatigue and Mental Well-Being in MS Patients(Multiple Sclerosis)
MS
Evaluation of the Effect of Quran Recitation on Fatigue and Mental Well-Being in MS Patients: A Randomized Controlled Trial
1 other identifier
interventional
52
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable multiple-sclerosis
Started Sep 2025
Shorter than P25 for not_applicable multiple-sclerosis
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 4, 2025
CompletedStudy Start
First participant enrolled
September 9, 2025
CompletedFirst Posted
Study publicly available on registry
April 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
April 22, 2026
April 1, 2026
8 months
July 4, 2025
April 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Fatigue Impact
The Fatigue Impact Scale (FIS)
1 mount
Secondary Outcomes (1)
Fatigue Severity Warwick-Edinburgh Mental Well-Being Scale
1 mount
Study Arms (2)
Experimental group
EXPERIMENTALThe 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.
Control group
NO INTERVENTIONPersonal 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.
Interventions
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 three days a week (Monday-Wednesday-Friday) and they will be asked to continue this practice for 4 weeks.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- Those with major psychiatric disorders
- Those with any obstacle to communication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Van Yüzüncü Yıl University Dursun Odabaş Medical Center
Van, 65200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Sevgi Demir Cam, Asst. Prof
Artvin Çoruh University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- The researcher and statistician will be blinded in order to maintain the validity of the research. Randomization will be performed by a single researcher who will not match. The researcher who will do the matching will be able to see which patient is in which group during the matching. The biased behavior of the researcher who does not adapt in this way will be exaggerated. After the matching, the participants will be entered into the SPSS program instead of writing the names of the groups, which will be named as 1st group and 2nd group, without giving information about which group is the group of listening to the Holy Quran, which group is the control group. It is planned to improve the quality of the innovation in these routes.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst. Prof. Dr
Study Record Dates
First Submitted
July 4, 2025
First Posted
April 22, 2026
Study Start
September 9, 2025
Primary Completion (Estimated)
May 15, 2026
Study Completion (Estimated)
May 15, 2026
Last Updated
April 22, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share