To check the relationship of back pain with lower spine and related factors among women.
Phase 1
- Registration Number
- CTRI/2020/05/025004
- Lead Sponsor
- Pfizer Inc
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Females over 18 years, who havenâ??t attained menopause .
Exclusion Criteria
Pregnancy, Postpartum up to 6 months, Bony or muscular abnormalities in the spine, pelvis and lower limbs (traumatic, congenital, infectious, systemic or post-surgical).
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) To identify the prevalence of chronic lumbopelvic pain among women. <br/ ><br>2) To identify the relationship between chronic lumbopelvic pain and pelvic asymmetry among women. <br/ ><br>Timepoint: total duration of study is 2 years. In the first 8 months, 2400 women will be assessed from 12 localities of Delhi through organization of camps in order to determine the prevalence of chronic lumbopelvic pain and identifying risk factors among women.
- Secondary Outcome Measures
Name Time Method To identify the risk factors associated with chronic lumbopelvic pain from a multidimensional approach.Timepoint: IN 2 months statistical analysis will be done. In next 6 months sensitization camps will be conducted, Based on the factors derived following analysis of risk factors from the participating women; camps/workshops will be organised for sensitization about chronic lumbopelvic pain.In the last 6 months final report will be prepared.