Patellofemoral pain syndrome. Patellofemoral disorders, unspecified knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Diagnosed patients with patellofemoral pain syndrome having three months history of pain Patients having positive clinical patellar test will be included
Exclusion criteria
Exclusion criteria: Patients with Osteoarthritis of knee joint, patellar tendinopathy will not be included Patients with Osgood Schlatter disease Those with recent history if fracture of knee joint will not be included in the trial Those who will have had history of malignancy will not be taken into account
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Primary outcome will be measured at baseline, 3rd and 6th week post intervention. Method of measurement: Pain will be assessed using Visual Analog Scale.;Functional disability. Timepoint: It will be assessed at Baseline, 3rd and 6th week post intervention. Method of measurement: It will be measured using Lower Extremity Functional Index.;Range of motion. Timepoint: Range of motion will be assessed at Baseline, 3rd and 6th week post intervention. Method of measurement: Range of motion will be measured using Goniometer. | — |
Countries
Pakistan
Contacts
Sialkot college of physical therapy Sialkot