- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04113460
The Effectiveness Yoga@Work Among Office Workers With Chronic Nonspecific Neck Pain (CNNP)
The Effectiveness Yoga@Work Among Office Workers With Chronic Nonspecific Neck Pain (CNNP): A Randomised Controlled Trial.
Chronic nonspecific neck pain (CNNP) is a public health issues with a 50% life prevalence. CNNP is a leading cause of disability which contributes to higher costs due to loss of productivity, disability, and increased absenteeism from work. Yoga has been found effective managing neck pain but there has been no study at work setting for chronic non-specific neck pain.
To determine the effectiveness of Yoga@work program for chronic non specific neck pain among office workers, present randomised controlled trial was undertaken.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Jaipur, India
- Yog Bhawan
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants who gave written informed consent
- Having neck pain for more than 3 month
Exclusion Criteria:
- Systematic disorder
- Neck or spine injuries
- Recent surgery
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Yoga Group
The yoga group received the 8-week yoga sessions at work setting once a week by trained teacher followed by self practices.
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Yoga@work program included physical movements, yoga posture, breathing exercise, pranayama and yoga chants.
Session with trainer was conducted on worksite once a week for an hour.
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No Intervention: Control Group
Participants had one introductory session on proper physical position and stretching exercises to be practiced daily during work.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neck Pain
Time Frame: Change from baseline to 8 weeks
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Pain was measured using Visual Analogue Scale
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Change from baseline to 8 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Health related quality of life
Time Frame: Change from baseline to 8 weeks
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HRQoL was measured with the Short Form 36
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Change from baseline to 8 weeks
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Neck function
Time Frame: change from baseline to 8 weeks
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Neck functions with Northwick Park Neck Pain Questionnaire
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change from baseline to 8 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Neha Sharma, PhD, Yog-Kulam
- Principal Investigator: Shekhar Sharma, NMP Medical Research Institute, India
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
- NMP/32491
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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