MedPath

Effects addition of patient education to hip and knee exercise on the pain of patient with patellofemoral pain syndrome

Not Applicable
Recruiting
Conditions
M22.2
patellofemoral pain syndrome.
Patellofemoral disorders
Registration Number
IRCT20240713062427N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Patients between 18 and 45 years old.
Self-reported anterior knee pain (unilateral or bilateral) when performing at least two of the following activities: prolonged sitting, squatting, kneeling, running, ascending and descending stairs, jumping and landing.
Self-reported anterior knee pain with insidious onset lasting at least 3 months.
Self- reported pain in the previous month should be at least 30 mm on a VAS scale of 100 mm.

Exclusion Criteria

Report of anterior knee pain caused by knee injury.
History report of patellar dislocation.
History of surgery in any lower limb joint.
Report any history of meniscus damage, ligament instability or patellar tendinopathy .
History of osteoarthritis in any lower limb joint.
Rheumatic or neurological disease reported by the patient.
Physiotherapy treatment for patellofemoral pain during the previous 6 months.
History of current or past psychosis, major depressive episode, attempted suicide, post-traumatic stress disorder, bipolar disorder, manic episode, or substance dependence.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analog Scale (VAS). Timepoint: They will be measured at the beginning of the study (before the intervention), immediately after the end of the treatment sessions (4 weeks) and two months after the end of the sessions. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath