Patellofemoral Pain. Segmental and somatic dysfunction of lower extremity
Conditions
Interventions
Intervention 1: The first intervention group: Resistance training of the thigh muscles will be done in eight weeks, three sessions a week and each session will last about 60 minutes with the presence
Sponsors
Bu ali Sina University, Hamedan
Eligibility
Sex/Gender
Female
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: 20 to 60 years Pain in the anterior and posterior part of the patella for more than 6 weeks Pain intensity 3 out of 10 on the visual analog scale Dynamic valgus angle of more than 10 degrees The positiveness of the stairs descent test and Clark No injuries in the hip and ankle joints No history of surgery or neurological disease Not having a history of participating in physical therapy in the past years
Exclusion criteria
Exclusion criteria: Deformity of Upper and Lower Limbs History of Surgery or Neurological Disease Injuries Other Than Patellofemoral Pain Knee Joint Instability Use of Painkillers Participation in Physiotherapy Sessions Participation in Sports Activities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: The For Evaluate be Will Use Visual Analogue Scale For Pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| Dynamic Knee Valgus. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: A Camera Will be Used to Evaluate the Dynamic Knee Valgus.;Strength of Hip Abductor Muscles. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: A Manual Dynamometer will be Used to Evaluate the Strength of Hip Abductor Muscles.;Plantar Pressure Distribution. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: A Foot Pressure Device Will be Used to Evaluate The Plantar Pressure Distribution.;Pain Catastrophic. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: Catastrophic Questionnaire Will be Used to Evaluate Catastrophic.;Static and Dynamic Balance. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: Biodex Device Will be Used to Evaluate Static and Dynamic Balance.;Knee Flexion. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: A Camera Will be Used to Evaluate the Knee Flexion.;Pelvic Drop. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: A Camera Will be Used to Evaluate the Pelvic Drop.;Rear-Foot Eversion. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervention. Method of measurement: A Camera Will be Used to Evaluate the Rear-Foot Eversion.;Dorsiflexion. Timepoint: The Timing of The Outcome Measure Will be Performed Before The Intervention and 8 Weeks After The Intervent | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Ali Yalfani
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Outcome results
None listed