The effect of ostrich oil on musculoskeletal disorders' pai
Not Applicable
Recruiting
- Conditions
- Musculoskeletal pain.Myalgia
- Registration Number
- IRCT2016122831631N1
- Lead Sponsor
- Prolife Company
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Being an adult and having musculoskeletal pain; Having no medical history of injection, surgery and topical medicine on the area.
Exclusion criteria:
No willingness for participation;
Requiring to use brace or cast;
Having other conditions such as CTS;
Requiring physical therapy;
Having history of surgery on the area .
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity. Timepoint: Before intervention, and 1 week(5-10 days), 2 weeks(10-16 days), one month(4-6 weeks) after intervention. Method of measurement: VAS and McGill questionnaire.
- Secondary Outcome Measures
Name Time Method Symptoms improvement time. Timepoint: At the begining and at the end of the trial. Method of measurement: VAS and McGill questionnaire.;Area of pain. Timepoint: Before and after the intervention. Method of measurement: using the area of pain diagram and software for calculating the area.;Quality of Life. Timepoint: Before and after intervention. Method of measurement: WHOQOL questionnaire.