SELH: Safety/Effectiveness Study of a Single Session of Laying-on-of-hands in Various Settings in Japan

Sponsor
MOA Health Science Foundation (Other)
Overall Status
Completed
CT.gov ID
NCT01316029
Collaborator
(none)
44,587
1
10
4478.9

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the symptomatic changes after a single session of laying-on-of-hands in various settings, and to evaluate optimal conditions for the outcomes.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Okada Purifying Therapy

Detailed Description

Laying-on-of-hands is applied in many different situations; however, most reports published previously described its efficacy in a clinical setting, with its administration conducted by a few expert practitioners. This study aimed to determine the symptomatic changes after a single session of the Okada Purifying Therapy, a form of laying-on-of-hands, in various settings, and to analyze factors influencing the outcomes.

Study Design

Study Type:
Observational
Actual Enrollment :
44587 participants
Observational Model:
Ecologic or Community
Time Perspective:
Cross-Sectional
Official Title:
A Large Cross-sectional Study of Laying-on-of-hands in Japan: Who Responds to it and What Facilitates the Response?
Study Start Date :
Feb 1, 2007
Actual Primary Completion Date :
Dec 1, 2007
Actual Study Completion Date :
Dec 1, 2007

Arms and Interventions

Arm Intervention/Treatment
laying-on-of-hands

44,587 Japanese volunteers with/without illness, who were interested in receiving laying-on-of-hands

Procedure: Okada Purifying Therapy
Each participant received a single session of Okada Purifying Therapy lasting 30 minutes or longer, administered by a voluntary certified practitioner.
Other Names:
  • laying-on-of-hands
  • biofield therapy
  • Therapeutic touch
  • Outcome Measures

    Primary Outcome Measures

    1. Severity of various symptoms [Baseline and immediately after a single intervention]

      Participants self-evaluated the severity of various symptoms before and after the intervention, and determined whether their symptoms got better, worsened, or did not change.

    Secondary Outcome Measures

    1. Adjusted odds ratios of the factors influencing the outcomes [in 1 year]

      After collecting all the eligible data, to be clarified are such personal variables as demographic attributes associated with the tendency to respond, and factors that facilitate such responses.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    16 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • able to receive laying-on-of-hands for 30 minutes or longer from the investigators

    • able to self-evaluate the change of their symptoms

    • competent to answer the Japanese questionnaires

    • aged 16 years or older

    Exclusion Criteria:
    • those who did not match the inclusion criteria

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 MOA Health Science Foundation Tokyo Japan 108-0074

    Sponsors and Collaborators

    • MOA Health Science Foundation

    Investigators

    • Principal Investigator: Kiyoshi Suzuki, MD, PhD, MOA Health Science Foundation

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01316029
    Other Study ID Numbers:
    • MHS-001
    First Posted:
    Mar 16, 2011
    Last Update Posted:
    Mar 16, 2011
    Last Verified:
    Jan 1, 2007

    Study Results

    No Results Posted as of Mar 16, 2011