None listed
Conditions
Interventions
None listed
Sponsors
Pfizer Inc
Eligibility
Inclusion criteria
Inclusion criteria: Females over 18 years, who havenâ??t attained menopause .
Exclusion criteria
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).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) To identify the prevalence of chronic lumbopelvic pain among women. 2) To identify the relationship between chronic lumbopelvic pain and pelvic asymmetry among women. 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
India
Contacts
Public ContactJasmine Kaur Chawla
Amity Institute of Physiotherapy
Outcome results
None listed