- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02837133
Effects of a Single Session of Integrated Yoga Therapy Compared With Other Relaxation Techniques
July 14, 2016 updated by: Hitoshi Okamura, Hiroshima University
Typically a course of yoga therapy for stress management takes place over a week, however, investigators are often asked to provide a single session for workers.
The aim of this study is to assess the benefits of a single session of an integrated yoga program compared with other relaxation techniques for the staff of schools.
Study Overview
Study Type
Interventional
Enrollment (Actual)
145
Phase
- Phase 3
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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- school staff members, including school managers, teachers, school nurses, school office workers, nutritionists and cooks
- volunteers attending a stress management workshop
Exclusion Criteria:
- those who had any previous experience of practicing yoga or any relaxation procedures
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
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: other techniques group
theory and practice of pair massage with tapping, stretching of the ankle and neck, and autogenic training
|
the program as a one-time session for 3 hours as a component of a Stress Management Education program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change of scores on the Subjective Units of Distress (SUD) scale
Time Frame: 1) immediately after the subjects arrived at the facility (baseline) and 2) immediately after the intervention
|
SUD is a scale of 0 (comfort) to 10 (discomfort) for measuring the subjective intensity of disturbance or distress currently experienced by an individual covering both physical and mental aspects.
|
1) immediately after the subjects arrived at the facility (baseline) and 2) immediately after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
March 1, 2014
Primary Completion (Actual)
December 1, 2015
Study Registration Dates
First Submitted
July 7, 2016
First Submitted That Met QC Criteria
July 14, 2016
First Posted (Estimate)
July 19, 2016
Study Record Updates
Last Update Posted (Estimate)
July 19, 2016
Last Update Submitted That Met QC Criteria
July 14, 2016
Last Verified
July 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- HiroshimaU
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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