Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome
Patellofemoral Pain Syndrome
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About this trial
This is an interventional treatment trial for Patellofemoral Pain Syndrome focused on measuring Patellofemoral pain syndrome, vibration, Planter/Dorsi ratio, pain
Eligibility Criteria
Inclusion Criteria: Age: Adults aged 18 -35 years Symptoms: Pain in the anterior or retro patellar knee region during activities such as running, jumping, squatting, or prolonged sitting Duration: Pain lasting at least 6 weeks Exclusion Criteria: Presence of other knee conditions: Individuals with PFPS who also have other knee conditions such as ligament or meniscal injuries, osteoarthritis, or patellar tendinopathy may be excluded. History of knee surgery: Patients who have undergone any knee surgery may be excluded as this may affect the outcomes of the study. Systemic conditions: Patients with systemic conditions that may affect the musculoskeletal system such as rheumatoid arthritis or lupus may be excluded. Pregnancy: Pregnant women with PFPS may be excluded as pregnancy may affect the outcomes of the study. Inability to comply with study requirements: Patients who are unable to comply with the study requirements such as attending follow-up appointments or completing questionnaires may be excluded.
Sites / Locations
- Faculty of physical therapy , cairo universityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
whole body viberation group
control group