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Clinical Trials/NCT04113473
NCT04113473
Completed
Not Applicable

Effectiveness of Yoga Therapy for Neck Pain Relief in Patients With Cervical Spondylosis

NMP Medical Research Institute1 site in 1 country62 target enrollmentDecember 11, 2018
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ConditionsCervical SpondylosisNeck Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervical Spondylosis
Sponsor
NMP Medical Research Institute
Enrollment
62
Locations
1
Primary Endpoint
Neck pain
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Cervical spondylosis is a chronic degenerative condition, commonly affecting >40-year-old adults worldwide. Cervical spondylosis is an important cause of neck pain and low back pain, and seriously affects the physical health, mental health, patients quality of life. Yoga has been most commonly used intervention for pain conditions. But its efficacy in cervical spondylosis has not yet been studied in clinical trials. The primary aim of the present study was to assess the efficacy of yoga chikitsa (therapy) compared with control intervention for neck pain caused by cervical spondylosis.

Registry
clinicaltrials.gov
Start Date
December 11, 2018
End Date
August 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Neck pain of CS as per diagnostic criteria of International Classification of Diseases
  • •CS supported by a physical examination, and cervical radiographic examination
  • •History of neck pain longer than 3 months
  • •willing to provide informed consent

Exclusion Criteria

  • •History of neck trauma, fracture or surgery,
  • •Systematic disease of the neck or spine including bones and joints conditions,
  • •Pregnancy

Outcomes

Primary Outcomes

Neck pain

Time Frame: Change from baseline to 12 weeks

ain intensity was measured by a 10-cm VAS scale, with 0 = "no Pain" and 10 = "the worst imaginable pain

Secondary Outcomes

  • Disability(Change from baseline to 12 weeks)
  • Health related Quality of Life(change from baseline to 12 weeks)

Study Sites (1)

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