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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04113473
Other study ID # NMP/62548
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 11, 2018
Est. completion date August 30, 2019

Study information

Verified date October 2019
Source NMP Medical Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date August 30, 2019
Est. primary completion date July 12, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Yoga Therapy
An hour of yoga therapy included loosening exercise (sukshma vyayama), yoga postures (asana), yoga breathing (pranayama), relaxation (shavasana) and meditation. Each participant were given handouts to follow home practice sessions everyday for twice a day for at least 15 minutes.

Locations

Country Name City State
India Pain Clinic, NMP Medical Research Institute Jaipur Rajasthan

Sponsors (2)

Lead Sponsor Collaborator
NMP Medical Research Institute Yog-Kulam, UK

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neck pain ain intensity was measured by a 10-cm VAS scale, with 0 = "no Pain" and 10 = "the worst imaginable pain Change from baseline to 12 weeks
Secondary Disability Neck disability was measured using neck disability index (NDI) score Change from baseline to 12 weeks
Secondary Health related Quality of Life Short Form-36 assessed the Quality of life change from baseline to 12 weeks
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