Healing Space Reiki Therapy: Effectiveness and Experiences

April 17, 2025 updated by: Herman van Wietmarschen, Louis Bolk Institute

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

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

Observational

Enrollment (Actual)

93

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

    • Utrecht
      • Bussum, Utrecht, Netherlands, 1402AD
        • Healing Space

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

No

Sampling Method

Non-Probability Sample

Study Population

Any adult person with any complaint contacting Healing Space for treatment

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

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

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

This is where you will find people and organizations involved with this study.

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)

August 1, 2017

Primary Completion (Actual)

October 1, 2023

Study Completion (Actual)

November 1, 2023

Study Registration Dates

First Submitted

April 9, 2025

First Submitted That Met QC Criteria

April 17, 2025

First Posted (Actual)

April 22, 2025

Study Record Updates

Last Update Posted (Actual)

April 22, 2025

Last Update Submitted That Met QC Criteria

April 17, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2025HSR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Anonymized MYMOP data and demographic data

IPD Sharing Time Frame

September 2024 till end of 2026

IPD Sharing Access Criteria

NAFKAM will access anonymized MYMOP and demographic data in excel format

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

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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