Sacroiliitis. Sacroiliitis, not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: participants aged between thirty and fifty years. Both genders Individuals with persistent pain in the lower back, gluteal, and groin regions Participants experienced lower extremity pain for more than four weeks but less than a year individuals who tested positive on pain provocation tests
Exclusion criteria
Exclusion criteria: Pregnant females Patients facing health issues hindering exercise, such as Systemic Lupus Erythematous (SLE), Multiple Sclerosis, and Chronic Fatigue Syndrome Individuals with osteoporosis affecting the pelvic and spine region Patients with inflammatory pathologies, including Ankylosing Spondylitis, Osteoarthritis Hip, and Degenerative Arthritis Those with a history of hip fracture or any spinal surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Before intervention and after 4 weeks. Method of measurement: NPRS.;Strength. Timepoint: Before intervention and after 4 weeks. Method of measurement: MMT.;Quality of life. Timepoint: Before intervention and after 4 weeks. Method of measurement: SF-36. | — |
Countries
Pakistan
Contacts
University of Lahore