Normal Healthy Individuals with patellofemoral pain syndrome..
Conditions
Interventions
Intervention 1: Intervention Group A will receive Compression Technique along with Mulligan's PRP. The treatment was administered three times a week for four weeks. Intervention 2: Intervention Group
Sponsors
None
Eligibility
Sex/Gender
All
Age
35 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age: 35 -65 years. Both Genders Symptoms positive for patellofemoral pain syndrome. Positive Clarke's Test Positive for provocative tests: patellar tracking, crepitus, J sign. Patients with grade-I Osteoarthritis
Exclusion criteria
Exclusion criteria: Age less than 35 or more than 65 years. Any Infection –Tuberculosis. Inflammation around the knee. Tumors around the knee. Rheumatoid Arthritis, trauma, ligamentous injury. Osteoporosis Any Red Flag Signs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale (VAS) for Pain. Timepoint: Before 1st Treatment session and after last Treatment session. Method of measurement: On VAS.;Knee Range of Motion (ROM). Timepoint: Before 1st Treatment Session and after Last Treatment session. Method of measurement: Measured by Standard Goniometer. | — |
Secondary
| Measure | Time frame |
|---|---|
| Lower Extremity Function scale (LEFS). Timepoint: Before 1st Treatment Session and after Last Treatment session. Method of measurement: The LEFS was completed by the patient him/her self and calculated by the therapist. | — |
Countries
Pakistan
Contacts
Public ContactWajida Perveen
Sialkot College of Physical Therapy, Amin Welfare & Teaching Hospital.
Outcome results
None listed