Efficacy of Adding Patellar Mobilization to Hip and Knee Exercises in Patients With Patellofemoral Pain Syndrome

August 19, 2024 updated by: Nadia Abdo Mohamed Abdelhafez, Cairo University

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

Detailed Description

this is interventional study in which patients will receive stretching and strengthening exercises in control group. in addition, experimental group will receive the same exercises of control group in addition to patellar mobilization, retinacula release and deep friction message.

Study Type

Interventional

Enrollment (Actual)

59

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Giza, Egypt
        • Cairo university

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Age ranging between 18 and 35 years
  2. Tenderness of medial and lateral borders of patella
  3. Retropatellar pain
  4. Duration of symptoms of patellofemoral pain syndrome is greater than 4 weeks
  5. Positive patellar compression test
  6. Pain intensity is more than 3 at visual analogue scale
  7. Had a history of insidious onset
  8. Had anterior knee pain during 2 or more of provocative activities that include stair ascent or descent, kneeling, prolonged sitting, or squatting

Exclusion Criteria:

  1. Previous patellar realignment surgery or patellar fracture
  2. Had a history of traumatic patellar dislocation
  3. Had a history of previous knee surgery
  4. Had any form of inflammatory arthritis that include osteoarthritis or rheumatoid arthritis
  5. Had a history of knee menisci, ligaments, bursae, or synovial plica syndrome dysfunction
  6. Taking corticosteroids or nonsteroidal anti-inflammatory medication
  7. Inability to attend treatment program to the end of sessions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

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.

Experimental: Group (2)
patients will receive stretch, strength, patellar mobilization, retinacula release and deep friction message

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
Changes in pain that felt during ascending, descending, squatting and prolonged sitting
Time Frame: It will be assessed one week before and after treatment
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.
It will be assessed one week before and after treatment
Changes in functional disability
Time Frame: It will be assessed one week before and after treatment
Functional disability will be assessed using Kujala questionnaire.The scale ranges from 0 to 100 score where 100 represents no functional limitation.
It will be assessed one week before and after treatment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in hip abductors strength
Time Frame: It will be assessed one week before and after treatment
It will be assessed using handheld dynamometer
It will be assessed one week before and after treatment
Changes in hip external rotators strength
Time Frame: It will be assessed one week before and after treatment
It will be assessed using handheld dynamometer
It will be assessed one week before and after treatment
changes in quadriceps strength
Time Frame: It will be assessed one week before and after treatment
It will be assessed using handheld dynamometer
It will be assessed one week before and after treatment
changes in functional performance
Time Frame: It will be assessed one week before and after treatment
It will be assessed using step down test
It will be assessed one week before and after treatment
changes in hamstring flexibility
Time Frame: It will be assessed one week before and after treatment
It will be assessed using 90-90 test
It will be assessed one week before and after treatment
changes in gastrocnemius flexibility
Time Frame: It will be assessed one week before and after treatment
It will be assessed using ankle dorsiflexion range of motion
It will be assessed one week before and after treatment
changes in knee valgus
Time Frame: It will be assessed one week before and after treatment
It will be assessed using Q angle
It will be assessed one week before and after treatment
changes in foot pronation
Time Frame: It will be assessed one week before and after treatment
It will be assessed using navicular drop test
It will be assessed one week before and after treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nadia A Mohamed, Msc, Assistant lecturer at orthopedic department of faculty of physical therapy

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2023

Primary Completion (Actual)

December 11, 2023

Study Completion (Actual)

March 18, 2024

Study Registration Dates

First Submitted

October 26, 2022

First Submitted That Met QC Criteria

December 22, 2022

First Posted (Actual)

December 27, 2022

Study Record Updates

Last Update Posted (Actual)

August 21, 2024

Last Update Submitted That Met QC Criteria

August 19, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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