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Trials / Completed

CompletedNCT03994809

International Study of Biofield Therapy

International Cross-sectional Study on the Effectiveness of Biofield Therapy for the Relief of Various Symptoms

Status
Completed
Phase
Study type
Observational
Enrollment
12,000 (actual)
Sponsor
MOA Health Science Foundation · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Accepted

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.

Detailed description

Participants aged 16 or older from 14 different countries (Japan, USA, Argentina, Brazil, Chile, Mexico, Peru, Taiwan, Thai, South Korea, Belgium, France, Portugal, and Spain) received a single session of biofield therapy (Okada Purifying Therapy) lasting 30 minutes or longer from the volunteer practitioners in their country of residence. Before and after the intervention, they reported each severity level of physical pain, anxiety/depression, dizziness/palpitation, and overall symptoms. The team compared the improvement/exacerbation rate of a single session of biofield therapy between the countries, and examined the adjusted odds ratio of the variables associated with the changes in each category of symptoms in a real-world setting.

Conditions

Interventions

TypeNameDescription
OTHEROkada Purifying TherapyThe 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.

Timeline

Start date
2008-01-01
Primary completion
2010-09-30
Completion
2010-09-30
First posted
2019-06-21
Last updated
2019-06-21

Source: ClinicalTrials.gov record NCT03994809. Inclusion in this directory is not an endorsement.