International Study of Biofield Therapy
International Cross-sectional Study on the Effectiveness of Biofield Therapy for the Relief of Various Symptoms
1 other identifier
observational
12,000
0 countries
N/A
Brief Summary
Participants from 14 different countries received a single session of biofield therapy (Okada Purifying Therapy) lasting 30 minutes or longer from the volunteer practitioners. Before and after the therapy, they reported the severity of physical pain, anxiety/depression, dizziness/palpitation, and overall symptoms. The team compared the effectiveness/safety of biofield therapy between countries and analyzed the factors associated with the outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2008
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2010
CompletedFirst Submitted
Initial submission to the registry
June 17, 2019
CompletedFirst Posted
Study publicly available on registry
June 21, 2019
CompletedJune 21, 2019
June 1, 2019
2.7 years
June 17, 2019
June 19, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
improvement/exacerbation rate of symptoms after a single session of biofield therapy
The Mann-Whitney test was conducted to compare the improvement/exacerbation rates between countries.
Up to one year after all the data were collected.
adjusted odds ratio of the factors associated with the changes in symptoms
Logistic regression analyses
Up to one year after all the data were collected.
Interventions
The practitioner raises his/her hand forward towards the recipient with the palm directed toward the recipient. The practitioner uses his/her hands alternately during the administration of Okada Purifying Therapy. The distance between the palm and the body is usually 1-2 feet, with each session typically lasting 30 to 60 minutes.
Eligibility Criteria
Participants were recruited in various settings, including the workshop, the investigator's house, or the participant's home in 14 different countries.
You may qualify if:
- Individuals who agreed to receive a single session of biofield therapy for 30 minutes or longer from the volunteer investigators.
- Individuals who were able to self-evaluate the change of their symptoms.
- Individuals who were competent to answer the questionnaires.
- Individuals who were aged 16 or older.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Suzuki K, Uchida S, Kimura T, Tanaka H, Katamura H. International Cross-Sectional Study on the Effectiveness of Okada Purifying Therapy, a Biofield Therapy, for the Relief of Various Symptoms. J Altern Complement Med. 2020 Aug;26(8):708-720. doi: 10.1089/acm.2019.0264. Epub 2020 Jun 17.
PMID: 32551797DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Kiyoshi Suzuki, MD, PhD
MOA Health Science Foundation
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- President
Study Record Dates
First Submitted
June 17, 2019
First Posted
June 21, 2019
Study Start
January 1, 2008
Primary Completion
September 30, 2010
Study Completion
September 30, 2010
Last Updated
June 21, 2019
Record last verified: 2019-06
Data Sharing
- IPD Sharing
- Will not share