- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05716373
The Effect of Reiki Application on Pain, Fatigue and Sleep Quality in Elderly Persons Staying in Nursing Homes
April 16, 2026 updated by: Gülcan Bahçecioğlu Turan, Ataturk University
A person's life is a stage that passes in the time interval that ends with his birth when he opens his eyes to the world and his death when he closes his eyes to the world.
Old age is a forced end for all people.
Sleep is one of the most important and basic human needs.
It prepares the individual for a new day by resting the body, strengthening and regulating the cerebral functions and repairing the brain.
While a change in sleep pattern and quality affects a person's daily life activities, long-term persistence of this change may lead to deterioration of body and mental health.During Reiki practices, the hands are held in each position for 3-5 minutes by touching the head, neck, chest, abdominal cavity and groin.
In problem areas, this time can be extended to 10-20 minutes.
The duration of treatment lasts an average of 30-90 minutes.
During the application, the person is in a lying or lying position and does not need to take off his clothes.
Study Overview
Detailed Description
In the elderly, the pathology of fatigue has not yet been fully elucidated.
Natural changes and the disadvantages of age can be the cause of fatigue.
Decrease in muscle strength, sarcopenia, pain, inactivity, changes in body composition due to malnutrition, decrease in physical fitness, insufficient energy systems, cardiovascular and respiratory problems, medications used can cause fatigue in the elderly.
It has been shown that 27-50% of the elderly suffer from moderate to severe fatigue.
Increasing the severity of fatigue reduces the daily activity performance of the elderly (6).
Today, in many areas, in addition to medical treatment to reduce the symptoms of chronic diseases, alternative and complementary medicine are also used.
Reiki, which constitutes our research subject; one of the energy approaches, in Japan at the end of the 19th century, Dr.
It is a complementary medicine application discovered by Usui in Sanskrit inscriptions, which has been shown to be effective on pain, depression, insomnia and fatigue symptoms.
Reiki is generally safe and no serious side effects have been reported.
Reiki practice in the last 10 years; it increases among physicians, nurses and other health workers.
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
-
-
Merkez
-
Elâzığ, Merkez, Turkey (Türkiye), 23000
- Gülcan B 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
50 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
• Being a nursing home resident and being 50 years or older,
- Not having a communication problem,
- Not having been diagnosed with bipolar disorder, schizophrenia or other mental illness,
- Not taking antidepressant treatment,
- Having chronic pain (arthralgia, back pain, musculoskeletal pain - at least once a day),
- Not using a pain reliever all the time,
- Willingness to participate in a four-week reiki program,
- Not having received body-mind therapy (yoga, reiki, massage, meditation) in the last six months.
- Having a scale score of >5 on the Piper Fatigue Scale
- A score of >5 on the Pittsburgh Sleep Quality Scale
- A scale score of >5 on the Visual Analog Scale
Exclusion Criteria:
- Needing antidepressant treatment,
- Not getting bored with work and not wanting to answer questions.
Exclusion Criteria:
-
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: Sequential Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental:
reiki will be aplicated
|
reiki
Other Names:
|
|
No Intervention: control
Routine maintenance will be applied.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pittsburgh Sleep Quality Index (PUKI);
Time Frame: 1 hours later
|
The scale is a safe and consistent questionnaire that evaluates the amount of sleep, sleep quality, presence and severity of sleep disorders in individuals in the last month.There are seven components in PUKI.
These components are subjective sleep quality (component 1), sleep latency (component 2), sleep duration (component 3), habitual sleep efficiency (component 4), sleep disturbance (component 5), sleep medication use (component 6) and daytime dysfunction.
(component 7).
The evaluation score of each item is between 0-3.
The total score obtained varies between 0-21.
The higher the score, the worse the sleep quality.
A score greater than five indicates poor sleep quality.
|
1 hours later
|
|
Piper Fatigue Scale
Time Frame: 1 hours later
|
The scale evaluates the individual's subjective perception of fatigue in four sub-dimensions.
These; behavior/violence sub-dimension evaluating the effect and severity of fatigue on activities of daily living (ADLs (6 items; 2-7); affect sub-dimension, which includes the emotional meaning attributed to fatigue (5 items; 8-12); it is the sensory sub-dimension (5 items; 13-17) that reflects the mental, physical and emotional symptoms of fatigue, and the cognitive/spiritual sub-dimension that reflects the effect of fatigue on cognitive functions and mental state (6 items; 18-23).
As a result of the average score; 0 points are interpreted as no fatigue, 1-3 points as mild fatigue, 4-6 points as moderate fatigue, 7-10 points as severe fatigue.
High scores obtained from the scale mean that the perceived fatigue level is high.
|
1 hours later
|
|
Visual Analog Scale (VAS) Evaluation
Time Frame: 1 hours later
|
The Visual Analog Scale (VAS) is used to convert some values that cannot be measured numerically.
Two end definitions of the parameter to be evaluated are written at the two ends of a 100 mm line, and the patient is asked to indicate where on this line their situation is appropriate by drawing a line or by placing a dot or pointing.
For example, for pain, I have no pain at one end and very severe pain at the other end and the patient marks his/her current state on this line.
The length of the distance from the point where there is no pain to the point marked by the patient indicates the patient's pain.
|
1 hours later
|
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)
December 1, 2022
Primary Completion (Actual)
January 6, 2023
Study Completion (Actual)
April 30, 2023
Study Registration Dates
First Submitted
January 28, 2023
First Submitted That Met QC Criteria
January 28, 2023
First Posted (Actual)
February 8, 2023
Study Record Updates
Last Update Posted (Actual)
April 21, 2026
Last Update Submitted That Met QC Criteria
April 16, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-97132852-050.01.04-162832
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.
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