- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05698797
Proprioceptive Training vs. Hip Abductor With External Rotator Strengthening in Patients With Patellofemoral Pain
January 16, 2023 updated by: Masood Khan, King Saud University
Effects of Proprioceptive Training vs. Hip Abductor With External Rotator Strengthening on Pain and Functions in Patients With Patellofemoral Pain Syndrome
Patellofemoral pain syndrome (PFPS) is a common musculoskeletal disorder characterized by an insidious onset of pain in the knee's anterior /retro-patellar / peripatellar region.
Even though various rehabilitation approaches, including hip strengthening and proprioceptive training, are being considered for managing PFPS, the most appropriate treatment from these two is still unclear.
Therefore, this study aimed to compare the program consisting of hip abductors and external rotators strengthening exercises vs. the program consisting of proprioceptive training of the knee to identify the most effective rehabilitation approach for patients suffering from PFPS.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
45
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
-
-
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Riyadh, Saudi Arabia, 11433
- King Saud University
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-
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
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age 18-35 years
- Patients diagnosed recently by an orthopedic surgeon for Patello-femoral pain syndrome
- experiencing anterior/retro patellar knee pain during activities,
- insidious onset of symptoms not linked to trauma,
- pain persisting for no less than four weeks,
- pain on palpation of the patellar facets,
- pain when stepping down from a 25-cm step or during a double-legged squat.
Exclusion Criteria:
- Patients with recent lower limb fractures or dislocations,
- knee/hip joint surgery,
- signs, symptoms, or radiological findings of intra-articular pathology such as effusion, ligamentous or meniscal involvement,
- those with indications of patellar apprehension,
- referred pain from the hip, back, or sacroiliac joint,
- acute knee strain or sprain,
- on medication such as NSAIDs or corticosteroids,
- degenerative and infectious arthritis
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group 1
In this group participants received hip abductor and external rotator strengthening exercises in addition to conventional physical therapy.
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Hip abductor and external rotator strengthening exercises were performed for 4 weeks.
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|
Active Comparator: Experimental group 2
In this group participants received proprioceptive training and conventional physical therapy.
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Proprioceptive training consisted of eight exercises was performed for 4 weeks.
|
|
Active Comparator: Control group
In this group participants received conventional physical therapy alone.
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Conventional physical therapy included interferential therapy and two types of knee-strengthening exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Kujala Anterior Knee Pain Scale (AKPS)
Time Frame: 4 weeks.
|
Pain was measured using the AKPS.
The AKPS is scored from a minimum score of 0 to a maximum score of 100 points.
Lower scores indicate greater pain and disability.
|
4 weeks.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 11, 2021
Primary Completion (Actual)
May 6, 2022
Study Completion (Actual)
June 24, 2022
Study Registration Dates
First Submitted
January 16, 2023
First Submitted That Met QC Criteria
January 16, 2023
First Posted (Estimate)
January 26, 2023
Study Record Updates
Last Update Posted (Estimate)
January 26, 2023
Last Update Submitted That Met QC Criteria
January 16, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AWH/EC/03/2021
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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.
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