- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06937359
Healing Space Reiki Therapy: Effectiveness and Experiences
Prospective Observational Study of Self-Reported Outcomes in Reiki Healing in the Netherlands Using the Measure Yourself Medical Outcomes Profile (MYMOP)
Reiki is an energetic healing method in which a therapist uses his hands on or near the clients body to channel life energy and send it to the client. This activates healing within the client and restores balance.
In this study clients at the Reiki training institute Healing Space are monitored for 4 weeks during 4 weekly Reiki healing sessions. Any client 18 years or older with any complaint can participate. A validated MYMOP questionnaire is used to monitor one main complaint, one secondary complaint and overall wellbeing after each of the 4 treatment sessions and before the start of treatment. A small number of clients will be interviewed for additional in depth data about their experiences. The aim of the study is to gain understanding about the effectiveness of Reiki.
Study Overview
Status
Intervention / Treatment
Detailed Description
Given the substantial international socio-economic burden of healthcare, the development of inexpensive, safe, and evidence-based treatments is highly desirable. Reiki, as a non-invasive and low-cost therapy, holds potential as a complementary approach to conventional medical treatments. However, the lack of consensus on its efficacy and mechanisms necessitates further investigation. This study aims to address these gaps by exploring the conditions clients report when visiting a Reiki healer and evaluating the subjective effectiveness and experiences of Reiki therapy. By doing so, the study seeks to contribute to the growing body of evidence on Reiki and inform its potential integration into healthcare systems.
This study is an observational prospective pre-post study with a convenience sample. The study is conducted at the Healing Space Reiki center in the Netherlands by Reiki practitioners trained at Healing Space. Each Reiki session lasts 1 hour and is conducted by 2 Reiki practitioners supervised by the founders of Healing Space. MYMOP questionnaires are provided before the first treatment (baseline) and then after each of the 4 treatments. A number of interviews is conducted after the complete treatment. All participants provided written informed consent. A waiver for full ethical assessment will be obtained from an ethical committee.
The MYMOP complaints are categorized into four primary groups: pain, psychological problems, fatigue, and other. Pre- and post comparisons of the four MYMOP measurements were performed usign paired t-tests and independent sample t-tests. Interviews are analysed thematically.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Utrecht
-
Bussum, Utrecht, Netherlands, 1402AD
- Healing Space
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Presence of any self reported complaint
- 18 years or older
- No other treatments for this complaint during the intervention period
Exclusion Criteria:
- Other treatments for the complaint during the intervention period
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self reported main symptom
Time Frame: 1 week
|
Self reported main symptom measured with the MYMOP questionnaire.
|
1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self reported secondary symptom
Time Frame: 1 week
|
Self reported secondary symptom with the MYMOP questionnaire
|
1 week
|
|
Overall wellbeing
Time Frame: 1 week
|
Self reported overall welbeing with the MYMOP questionnaire
|
1 week
|
Collaborators and Investigators
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
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
- ANALYTIC_CODE
- CSR
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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