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Patello Femoral Pain Syndrome

Not Applicable
Conditions
ormal Healthy Individuals with patellofemoral pain syndrome..
Registration Number
IRCT20201031049207N2
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
45
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
ower 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.
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