- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05342610
Effect of Reiki Application on Menopausal Symptoms
In this randomized controlled study, it was aimed to determine the effect of distant reiki on menopausal symptoms. Two different hypothesis teams have been established for the study.
These; H0: There is no significant difference between the menopause rating scores of the women in the study group in which distant reiki was applied and the control group without distant reiki.
H1: There is a significant difference between the menopause rating scores of the women in the study group in which distant reiki was applied and the control group without distant reiki.
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Mersin, Turkey, 33110
- Diğdem LAFCI
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Willing to participate in research,
- Can read and write in Turkish,
- Open to communication,
- Those who are between the ages of 40-55 and do not experience menstruation for at least one year,
- Experiencing at least one or more of the menopausal symptoms,
- Not applying regular reiki,
- Those who have not surgically entered menopause,
- Women without psychiatric problems
Exclusion Criteria:
- Who do not agree to participate in the research,
- Can't read and write Turkish,
- Communication is not possible,
- Those who are younger than 40, older than 55, have experienced menstruation for at least one year,
- Do not experience the symptoms of menopause,
- Using medication for the treatment of menopausal symptoms,
- Chronic illness,
- Regular reiki is applied,
- Surgically in menopause,
- Women with psychiatric problems
Study Plan
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 |
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Experimental: Experimental (distant reiki) group
Reiki (complementary and integrative medicine method) was applied individually to the experimental group for 30 minutes three times a week for four weeks.
Data collection forms was applied 3 times in total, before the intervention, in the fourth and the eighth week.
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Reiki; It is the transfer of energy to other people by the hands of the person who receives the theoretical training and attunement (initiation) from the reiki master, close or distant.
When the hands are brought closer to the body in suitable positions or when the reiki practitioner visualizes the person in his/her thoughts, the energy flow starts spontaneously and the transferred energy is shaped according to the needs of the reiki recipient.
The biggest advantage of Reiki; It is an easy and cost-effective method to ensure that the individual restores the balance between body, mind and spirit, has no side effects, has no negative effects on behavior and attitudes.
Other Names:
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No Intervention: Control group
No intervention was made to women in the control group.
However, data collection forms was applied 3 times in total, before the intervention, in the fourth and the eighth week.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Menopause symptoms evaluated using the Menopause Rating Scale
Time Frame: Change from before intervention, 4th and 8th week of intervention
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It was developed in German by Schneider et al.
In 1992 to measure the severity of menopausal symptoms and was adapted to English in 1996.
MRT was adapted to Turkish by Gürkan in our country in 2005.
There are "0 = None", "1 = Mild", "2 = Moderate", "3 = Severe" and "4 = Very severe" options for each item in the Likert-type scale consisting of 11 items including menopausal complaints.
The total score of the scale is calculated based on the scores given for each item.
The lowest score that can be obtained from the scale is 0, the highest score is 44.
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Change from before intervention, 4th and 8th week of intervention
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MersinUnivers
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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