Chronic Low-back Pain Clinical Trial
Official title:
To Observe The Effectiveness Of Cat-Cow Yoga In The Pain Management Of Chronic Low Back Pain In Health Care Professionals
Verified date | February 2023 |
Source | University of Karachi |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A randomized control trial is planned to investigate the effectiveness of Cat-Cow yoga as a treatment for chronic low back pain CLBP. An 12 weeks course of intervention will be provided to the candidates that will meet the eligibility criteria of the study. Substance P, beta endorphins and cortisol will be tested both the groups' pre and post treatment and then the difference from the baseline value will be determined.
Status | Completed |
Enrollment | 100 |
Est. completion date | January 20, 2023 |
Est. primary completion date | December 15, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years to 45 Years |
Eligibility | Inclusion Criteria: Answer Yes to the following questions. 1. Have low back pain constantly or on most days for the last three months. 2. Have you seek care from health care provider due to back pain 3. Average pain intensity, assessed using the Numerical Pain Rating (NPR) scale over the past week = 2 on a 0-10 numerical pain scale. 4. Roland Morris Disability Questionnaire score = 4. 5. Fear Avoidance Beliefs Questionnaire (FABQ) work subscale score <19. Exclusion Criteria: - To be eligible for the study participants must not: - Have a personal history of the following neurological disorders: Alzheimer's, Amyotrophic Lateral Sclerosis, Multiple Sclerosis, Parkinson's, Stroke - Have a personal history of the following cardiorespiratory disorders: Congestive heart failure, Heart attack in past 24 months - Have a personal history of the following musculoskeletal disorders: Rheumatoid Arthritis, pathologic fractures of the spine, avascular necrosis or osteonecrosis, severe osteoarthritis. Including a history of spine surgery or a hip arthroplasty - Have active cancer - Be Blind - Report being pregnant, lactating, or that they anticipate becoming pregnant in the next 3-months - Have a body mass index greater than 35 kg/m2 - Have clinical depression (i.e., subjects who score 24 or higher on the Center for Epidemiology Depression Scale). - Have used narcotics or muscle relaxants within 30 days prior to study enrollment. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Koohi Goth Women Hospital | Karachi | Sindh |
Lead Sponsor | Collaborator |
---|---|
University of Karachi |
Pakistan,
Alleva J, Hudgins T, Belous J, Kristin Origenes A. Chronic low back pain. Dis Mon. 2016 Sep;62(9):330-3. doi: 10.1016/j.disamonth.2016.05.012. Epub 2016 Jun 22. No abstract available. — View Citation
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain Score | It will assessed with the help of Numeric Pain Rating Scale. using a 0-10 scale, where 0 corresponds to "no pain" and 10 to "the greatest pain possible." | 3 Months | |
Primary | Extent of Disability | It will be detected with the help of Oswestry Low Back Pain Disability Questionnaire. This index is considered a standard to assess low back functionality, it has a total of 10 sections, and for each section with a possible score 5. The percentage improvement is calculated through the total possible score x 100. | 3 Months | |
Secondary | Substance P | Changes in the levels of Substance P will be observed during the span of the study in test and control groups. | 3 Months | |
Secondary | Beta Endorphins | Changes in the levels of beta endorphins will be observed during the span of the study in test and control groups. | 3 Months | |
Secondary | Stress Score | Physical stress of the participants will be evaluated with Sadaf Stress Scale (SSS) before and after the therapy in both the groups. | 3 Months | |
Secondary | Cortisol | Changes in the levels of Cortisol will be observed during the span of the study in test and control groups. | 3 Months | |
Secondary | Quality of Life Score | This measure will be evaluated from baseline to post intervention with the help of World Health organization Quality of Life (WHOQOL) Questionnaire | 3 Months |
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