Effects of Reiki and Self-Acupressure Applications
Comparison of the Effects of Reiki and Self-Acupressure Applications on Functionality and Quality of Life in Patients With Multiple Sclerosis: A Randomized Controlled Trial
1 other identifier
interventional
50
1 country
1
Brief Summary
Reiki, the subject of our research, is a complementary medicine practice within energy approaches. Discovered in Sanskrit texts by Dr. Usui in Japan in the late 19th century, it was demonstrated through studies demonstrating its effectiveness in symptoms of pain, depression, insomnia, and fatigue. Everything in the universe, including the human body, is composed of energy; any disruption in this energy can lead to illness. There are seven chakras where Reiki is applied. The main chakra centers are located along the spine. During Reiki treatments, the hands are held in each position, touching the head, neck, chest, abdominal cavity, and groin for 3-5 minutes. This period may extend to 10-20 minutes in problematic areas. The average treatment duration is 30-90 minutes. During the treatment, the patient lies down or reclines, and there is no need to remove clothing. During Reiki treatment, individuals may report a slight warming sensation under or near the therapist's hand. The only rule in Reiki practice is that the individual gives the practitioner permission to facilitate the flow of energy. The person receiving Reiki does not need to believe in Reiki during the treatment. Reiki is a universal life energy present in everyone. Reiki is generally safe, and no serious side effects have been reported. Over the last 10 years, Reiki practice has been increasing among physicians, nurses, and other healthcare professionals. This study will compare the effects of acupressure and Reiki treatments on functionality and quality of life in patients with multiple sclerosis.
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 Apr 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
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 20, 2025
CompletedFirst Submitted
Initial submission to the registry
July 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 20, 2025
CompletedFirst Posted
Study publicly available on registry
July 24, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 20, 2025
CompletedJuly 24, 2025
July 1, 2025
3 months
July 17, 2025
July 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
The Multiple Sclerosis Quality of Life
The Turkish adaptation of the scale was conducted by Tülek in 2006. Tülek found Cronbach's alpha reliability coefficients to be 0.94 for the composite physical health and 0.89 for the composite mental health. This scale was created by adding 18 items related to MS-specific problems to the items related to general health perception (5 items), energy/fatigue (5 items), social functioning (2 items), emotional well-being (5 items), role limitations due to emotional problems (3 items), physical functioning (10 functions), role limitations due to physical problems (4 items), pain (3 items), and health changes found in the SF-36, a widely used generic quality of life scale for many conditions. The MSQOL-54 Quality of Life Scale consists of two main groups: physical health composite and mental health composite, 13 subgroups, and two independent items. Scores range from 0 to 100, with higher scores indicating higher quality of life.
4 weeks
The Multiple Sclerosis Functional Composite
The Scale consists of three subtests: the "9-Hole Peg Test" that evaluates upper extremity functions, the "25-Step Walking Test" that checks lower extremity functions, and the "Step Auditory Serial Addition Test" that evaluates immediate memory and cognitive functions. It was administered within the MSFC.
4 weeks
Study Arms (3)
Reiki group
EXPERIMENTALGroup where Reiki was applied
Self-acupressure applied group
EXPERIMENTALGroup where Self-acupressure was applied
Control
NO INTERVENTIONGroup with no intervention
Interventions
Eligibility Criteria
You may qualify if:
- Patients who are willing to participate
- Patients who have no communication problems
- Patients who are 18 years of age or older
- Patients who live in the center
- Patients who have no scratches or deformities in the treatment area
- Patients who do not smoke, use drugs, or use tranquilizers, and are not pregnant
- Patients who have been receiving MS treatment for more than three months
You may not qualify if:
- Patients who smoke, use substances, or use tranquilizers
- Have dyspnea
- Have anemia
- Have diabetes
- Have received corticosteroid treatment in the last three months
- Have had an MS attack in the last three months
- Have an autoimmune disease other than multiple sclerosis
- Have signs of infection
- Have a thyroid problem
- Are taking psychostimulant medications
- Have anxiety or depression detected in outpatient clinic screenings
- Refuse to participate in the study
- Have another known neurological system disease (dementia, Alzheimer's, etc.)
- Have a communication barrier will not be included in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Firat Universitylead
Study Sites (1)
Muğla Sıtkı Koçman University
Muğla, Fethi̇ye, 48300, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Caner F Demir, MD
Firat University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The groups doing the analysis will do the analysis without knowing it.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
July 17, 2025
First Posted
July 24, 2025
Study Start
April 20, 2025
Primary Completion
July 20, 2025
Study Completion
September 20, 2025
Last Updated
July 24, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share