IRCT20240211060958N2
Recruiting
Phase 3
Comparison of the effect of neurodynamic mobilization and dry needling technique on the pain, function, and range of motion in subjects with patellofemoral pain syndrome
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- patellofemoral pain syndrome.
- Sponsor
- Kerman University of Medical Sciences
- Enrollment
- 120
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All participants are aged from 18 to 40 years
- •Having a clinical diagnosis of patellofemoral syndrome.
- •Complaints of pain in the anterior of the knee or around the patella on the affected side are determined during at least 3 of the following activities: squatting, step up and down from stairs, running, prolonged sitting, and kneeling.
- •Positive Clark test
- •Unilateral pain in one knee
- •having constant pain for at least the last 4 weeks and the average pain in the last week is more than 3 according to the NPRS scale.
- •The present of trigger points in the gluteus medius and quadriceps muscles on the same side and quadratus lumborum on the opposite side.
Exclusion Criteria
- •History of previous knee surgery
- •Any knee pathology (meniscus tear, patella tendinopathy, ligament sprain and osteoarthritis)
- •Any systemic diseases and/or connective tissue disorders
- •People who have received acupuncture, injections, or dry needling treatment for knee in the past 6 months.
- •Pregnant women
Outcomes
Primary Outcomes
Not specified
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