- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06128668
The Effect of Yoga on Sleep Quality, Fatigue and Physical Activity Level of Multiple Sclerosis
December 10, 2024 updated by: Gülcan Bahçecioğlu Turan, Ataturk University
The Effect of Yoga on Sleep Quality, Fatigue and Physical Activity Level of Multiple Sclerosis Patients: A Randomized Controlled Study
This randomized controlled study will be conducted to examine the effects of Yoga on Sleep, Fatigue and Physical Activity in Individuals Diagnosed with Relapsing-Remitting Multiple Sclerosis.
Study Overview
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Elazığ, Turkey
- Gülcan Bahçecioğlu TURAN
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
Patients diagnosed with Relapsing-Remitting Multiple Sclerosis Being an adult between the ages of 18-65
Exclusion Criteria:
- Those who have communication problems Those with psychiatric problems Having a condition that prevents you from doing yoga
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Yoga
Yoga will be aplicated
|
Yoga will be applied
|
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No Intervention: Control
Yoga will not be aplicated
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pittsburgh Sleep Quality Index
Time Frame: Six week
|
A reliable distinction can be made at the desired level between "good sleepers" and "poor sleepers".
The scale contains a total of 24 questions, 19 of which are self-evaluation questions. 5 of them are answered by the individual's spouse or roommate, are used only for clinical information and are not included in the scoring.
Question 19, one of the self-assessment questions, is about whether there is a roommate or spouse and is not taken into account in determining the total and component scores of the scale.
Scale questions that determine sleep quality include different factors related to sleep quality.
These questions are to determine sleep duration, sleep latency, and the frequency and severity of specific sleep-related problems.
The 18 items scored were grouped into 7 component scores.
|
Six week
|
|
Fatigue Severity Scale:
Time Frame: six week
|
The Fatigue Severity Scale is used in most studies evaluating fatigue in MS.
The scale consists of 9 questions.
Each question consists of 7 points.
High scores indicate fatigue.
The validity and reliability studies of the scale for Turkey were conducted by Armutlu et al. in 2007, and the Turkish version was also found to be valid and reliable.
The scales include the day they were filled in and inquire about fatigue status in the last month.
The Fatigue Severity Scale was developed in the 1980s to facilitate the research and treatment of fatigue and to distinguish fatigue from depression and somatic disorders.
The survey demonstrated good internal consistency when repeated and across disease responses.
The validity of the questionnaire was found to be higher in MS patients.
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six week
|
|
Expanded Disability Status Scale (EDSS, ExpandedDisabilityStatusScala):
Time Frame: six week
|
This test, created by Kurtzke, measures disability and neurological symptoms in MS patients.
A score is given between 0 and 10. 0 indicates no disability or disorder, while 10 indicates death due to MS. MS patients were divided into 2 groups according to their EDSS scores.
EDSS = 6 (requires cane, crutches or other aids to walk)
|
six week
|
|
International Physical Activity Questionnaire (IPAQ):
Time Frame: six week
|
It obtains data on sitting, walking, moderate-intensity activities and time spent in vigorous activities.
In evaluating all activities, the criterion is that each activity should be done for at least 10 minutes at a time.
A score as METmin/week is obtained by multiplying the minute, day and MET value.
After scoring, physical activity levels are classified as physically inactive (inactive), low physical activity level (minimally active) and sufficient physical activity level (very active).
It has short and long forms, and the short form is generally used in studies.
The short form consists of 8 questions
|
six week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 25, 2023
Primary Completion (Actual)
March 25, 2024
Study Completion (Actual)
July 25, 2024
Study Registration Dates
First Submitted
October 24, 2023
First Submitted That Met QC Criteria
November 7, 2023
First Posted (Actual)
November 13, 2023
Study Record Updates
Last Update Posted (Estimated)
December 13, 2024
Last Update Submitted That Met QC Criteria
December 10, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 338394
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.