- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01927250
Influence of Multi-dimensional Wellness Program on Quality of Life (MDWP)
October 17, 2023 updated by: Kiyoshi Suzuki, MOA Health Science Foundation
Influence of Multi-dimensional Wellness Program (Diet, Art and Biofield Therapy) on Quality of Life in Japanese Population
The purpose of this study is to determine whether multi-dimensional wellness program (diet, art and biofield therapy) influences the quality of life for those with different health status in Japan.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Combination of wellness programs may be one of the best approaches to improve quality of life; however, the effectiveness of a treatment that combines various programs is also yet to be clarified.
This study investigated the influence of Okada Health and Wellness program on the quality of life for healthy people and those with illness in Japan.
Okada Health and Wellness program consists of 3 components: diet, art and biofield therapy.
Study Type
Interventional
Enrollment (Actual)
12166
Phase
- Not Applicable
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
-
-
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Tokyo, Japan, 108-0074
- MOA Health Science Foundation
-
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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
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Those who were interested in practicing the diet program and art therapy established by the MOA International Corporation.
- Able to receive Okada Purifying Therapy, a domain of biofield therapy at least once a week.
- Competent to answer the Japanese questionnaires for quality of life
- Aged 16 years or older
Exclusion Criteria:
- Those who did not match the inclusion criteria
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
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Okada Health and Wellness program
12,166 Japanese volunteers with/without illness, who were interested in practicing Okada Health and Wellness program for 3 consecutive months.
|
Each participant were encouraged to practice the diet program and art therapy established by the MOA International Corporation, and to receive Okada Purifying Therapy, a domain of biofield therapy, for 3 consecutive months.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change of quality of life
Time Frame: baseline and after 3 months
|
Participants were encouraged to practice Okada Health and Wellness program during the intervention period (3 months).
They completed a quality of life questionnaire before and after the intervention period.
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baseline and after 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adjusted odds ratios of the factors associated with the change of quality of life.
Time Frame: in 1 year
|
After collecting all the eligible data, to be clarified are such personal variables as demographic factors and the 3 components of Okada Health and Wellness program that influence the quality of life.
|
in 1 year
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kiyoshi Suzuki, MD, PhD, MOA Health Science Foundation
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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
February 1, 2007
Primary Completion (Actual)
December 1, 2007
Study Completion (Actual)
March 1, 2008
Study Registration Dates
First Submitted
August 17, 2013
First Submitted That Met QC Criteria
August 19, 2013
First Posted (Estimated)
August 22, 2013
Study Record Updates
Last Update Posted (Actual)
October 19, 2023
Last Update Submitted That Met QC Criteria
October 17, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MOA-003
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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