- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04313413
Yoga@Work for Reducing Musculoskeletal Pain in Neck and Shoulder
Effectiveness of Yoga@Work Program for Reducing Musculoskeletal Pain in Neck and Shoulder: Evaluation Study
Work-related musculoskeletal disorders (MSDs) are disorders of muscles, tendons, joints and nerves which can affect all body parts, although the neck, upper limb and back are the most common areas.
The peer-reviewed literature about workplace prevention describes a variety of interventions that have been implemented and evaluated.but only few studies show sustainable positive effects on symptom outcomes.
Yoga@Work program was developed to self manage pain around neck and shoulder areas among office workers.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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London, United Kingdom
- Yog Kulam
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Office workers
- Willing to participate and give consent
- non specific neck and shoulder pain
Exclusion Criteria:
- neck injury
- Trauma
- Cancer related pain
- psychiatric disorder/ medication
- Pregnancy
Study Plan
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: Yoga@Work
Yoga sessions specifically designed for office workers were provided in work settings.
participants were given handouts and encouraged to practice in their own time and space during work days.
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Yoga sessions includes sukshma vyayama (strengthening yoga expertise), stretching and relaxing postures (asana) on chair or standing, breathing and meditation practices.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neck and Shoulder pain
Time Frame: From baseline to 4-week post intervention
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self reported neck and shoulder pain using visual analogue scale on 0 to 10 scale, where 0 is no pain and 10 is worst pain.
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From baseline to 4-week post intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Global Outcome
Time Frame: from baseline to 5 week post intervention
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Patient Global Received Rating of Improvement or Satisfaction
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from baseline to 5 week post intervention
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Monomita Nandy, Brunel University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AU03
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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