Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome
Patellofemoral Pain Syndrome
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