- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04313517
Yoga@Work Intervention to Reduce Work-related Stress Among Information Technology Workers
March 18, 2020 updated by: Aarogyam UK
Yoga@Work Intervention to Reduce Work Related Stress Among Information Technology Workers: Waitlist Controlled Trial
Over the last several decades, occupational stress at workplace comprise a major burden.
Office based work are more prone to sedentary lifestyle, postural issues, workplace stress, repetitive strain injury, poor employee health.
Workplace wellness programs has been very feasible access to employees at their own convenience and need.
Yoga@Work Program was developed to suit the need for information technology workers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
140
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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Brussels, Belgium
- UNRI
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Hong Kong, Hong Kong
- Ananda Yoga
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Rajasthan
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Jaipur, Rajasthan, India
- NMP Medical Research Institute
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London, United Kingdom
- Yog-Kulam
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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
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Information Technology employee, or trainee willing and able to participate in a 6-week self-care program during the work day.
- Willing to give informed consent
Exclusion Criteria:
- medical or psychiatric conditions limiting practice of yoga in general
- Cognitive impairment
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Yoga@Work
Yoga session were developed to practice at work anytime feasible.
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Each yoga session included warm-up practices (for the large joints, spine, and extremities), Simple postures (Asana), breathing exercises (pranayama) and meditation/relaxation.
All the yoga participants were given handouts to practice everyday at work as its feasible
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No Intervention: Wait list Control group
Control group with no intervention.
After Intervention period, group was offered same sessions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reductions in occupational stress
Time Frame: From baseline to 6-week post intervention
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Perceived Stress Scale
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From baseline to 6-week post intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mental health problems
Time Frame: From baseline to 6-week post intervention
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General Health questionnaires consists of 12 items, each assessing the severity of a mental problem
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From baseline to 6-week post intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Monomita Nandy, Brunel University
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 (Actual)
January 12, 2019
Primary Completion (Actual)
June 18, 2019
Study Completion (Actual)
September 21, 2019
Study Registration Dates
First Submitted
March 17, 2020
First Submitted That Met QC Criteria
March 17, 2020
First Posted (Actual)
March 18, 2020
Study Record Updates
Last Update Posted (Actual)
March 19, 2020
Last Update Submitted That Met QC Criteria
March 18, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AUI01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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