- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05665452
Efficacy of Adding Patellar Mobilization to Hip and Knee Exercises in Patients With Patellofemoral Pain Syndrome
Patellofemoral pain syndrome is a common source of anterior knee pain. The causes of PFPS may be multifactorial such as biomechanical disorders, muscle weakness which affect the dynamic stability of lower limb and alter patellar tracking in trochlear groove. Moreover, the syndrome associated with muscular tightness of iliotibial band, gastrocnemius, soleus, hamstring and quadriceps. Strengthening and stretching exercises are effective in improving patient's symptoms. However, they do not sufficient in correction of kinematic changes associated with PFPS. Patellar mobilization is effective in improving patient'symptoms in cases with PFPS. However, studies that conducted patellar mobilization were either low quality studies or no study combined patellar mobilization with hip and knee exercises.
Therefore, APTA guidelines recommended for conducting high quality study to investigate the effect of adding patellar mobilization to exercise therapy to support the definite recommendation delivered to therapists.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Giza, Egypt
- Cairo university
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age ranging between 18 and 35 years
- Tenderness of medial and lateral borders of patella
- Retropatellar pain
- Duration of symptoms of patellofemoral pain syndrome is greater than 4 weeks
- Positive patellar compression test
- Pain intensity is more than 3 at visual analogue scale
- Had a history of insidious onset
- Had anterior knee pain during 2 or more of provocative activities that include stair ascent or descent, kneeling, prolonged sitting, or squatting
Exclusion Criteria:
- Previous patellar realignment surgery or patellar fracture
- Had a history of traumatic patellar dislocation
- Had a history of previous knee surgery
- Had any form of inflammatory arthritis that include osteoarthritis or rheumatoid arthritis
- Had a history of knee menisci, ligaments, bursae, or synovial plica syndrome dysfunction
- Taking corticosteroids or nonsteroidal anti-inflammatory medication
- Inability to attend treatment program to the end of sessions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group (1)
patients will receive stretch and strength exercises
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All exercises will be performed for 30 to 45 minutes per session, 3 times per week for 4 weeks (12 sessions). Group (1): stretch exercises are performed for calf, hamstring, iliotibial band and quadriceps. strength exercises consist from open kinetic chain (hip abductors, hip external rotators and quadriceps) and closed kinetic chain exercises (mini wall squat exercise, forward step up exercise, lateral step up exercise and terminal knee extension exercise). Group (2): stretch exercises are performed for calf, hamstring, iliotibial band and quadriceps. strength exercises consist from open kinetic chain (hip abductors, hip external rotators and quadriceps) and closed kinetic chain exercises (mini wall squat exercise, forward step up exercise, lateral step up exercise and terminal knee extension exercise). manual therapy consists from iliotibial band release, deep friction message for lateral retinacula and medial patella mobilization. |
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Experimental: Group (2)
patients will receive stretch, strength, patellar mobilization, retinacula release and deep friction message
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All exercises will be performed for 30 to 45 minutes per session, 3 times per week for 4 weeks (12 sessions). Group (1): stretch exercises are performed for calf, hamstring, iliotibial band and quadriceps. strength exercises consist from open kinetic chain (hip abductors, hip external rotators and quadriceps) and closed kinetic chain exercises (mini wall squat exercise, forward step up exercise, lateral step up exercise and terminal knee extension exercise). Group (2): stretch exercises are performed for calf, hamstring, iliotibial band and quadriceps. strength exercises consist from open kinetic chain (hip abductors, hip external rotators and quadriceps) and closed kinetic chain exercises (mini wall squat exercise, forward step up exercise, lateral step up exercise and terminal knee extension exercise). manual therapy consists from iliotibial band release, deep friction message for lateral retinacula and medial patella mobilization. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes in pain that felt during ascending, descending, squatting and prolonged sitting
Time Frame: It will be assessed one week before and after treatment
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Pain during ascending, descending, squatting and prolonged sitting will be assessed using visual analogue scale, it is a horizontal line from 0 to 10, where 0 no pain and 10 maximum pain.
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It will be assessed one week before and after treatment
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Changes in functional disability
Time Frame: It will be assessed one week before and after treatment
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Functional disability will be assessed using Kujala questionnaire.The scale ranges from 0 to 100 score where 100 represents no functional limitation.
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It will be assessed one week before and after treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes in hip abductors strength
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using handheld dynamometer
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It will be assessed one week before and after treatment
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Changes in hip external rotators strength
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using handheld dynamometer
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It will be assessed one week before and after treatment
|
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changes in quadriceps strength
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using handheld dynamometer
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It will be assessed one week before and after treatment
|
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changes in functional performance
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using step down test
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It will be assessed one week before and after treatment
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changes in hamstring flexibility
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using 90-90 test
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It will be assessed one week before and after treatment
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changes in gastrocnemius flexibility
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using ankle dorsiflexion range of motion
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It will be assessed one week before and after treatment
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changes in knee valgus
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using Q angle
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It will be assessed one week before and after treatment
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changes in foot pronation
Time Frame: It will be assessed one week before and after treatment
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It will be assessed using navicular drop test
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It will be assessed one week before and after treatment
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nadia A Mohamed, Msc, Assistant lecturer at orthopedic department of faculty of physical therapy
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004020
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Patellofemoral Pain Syndrome
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University of North Carolina, Chapel HillCanadian Institutes of Health Research (CIHR)CompletedPatellofemoral Pain Syndrome | Patellofemoral Pain (PFPS) | Patellofemoral Pain | Patellofemoral Pain, PFPUnited States
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Lauren EricksonAmerican College of Sports MedicineCompleted
-
Beijing Sport UniversityCompletedPatellofemoral PainChina
-
Boston Children's HospitalEnrolling by invitationPatellofemoral PainUnited States
-
Beijing Sport UniversityNot yet recruitingPatellofemoral Pain, PFP
-
Beijing Sport UniversityNot yet recruiting
-
Istanbul University - CerrahpasaRecruitingPatellofemoral Pain, PFPTurkey (Türkiye)
-
Pamukkale UniversityNot yet recruitingPatellofemoral Pain, PFPTurkey (Türkiye)
-
Ahram Canadian UniversityNot yet recruitingPatellofemoral Pain (PFPS)Egypt
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Beijing Sport UniversityCompletedPatellofemoral Pain, PFPChina