- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07305610
INFLUENCE OF SELECTED POSITIONS ON HIP ABDUCTORS STRENGTH AND ACTIVATION IN PATELLOFEMORAL PAIN SYNDROME IN MALES (PFPS)
December 13, 2025 updated by: Mohamed Gouda Mohamed, Ahram Canadian University
The study aims to explore the effect of body position (side-lying versus standing) on hip abductors muscle strength and activation in individuals with and without PFPS and then to compare these measures between the two groups in each position
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
A cross-sectional comparative study involving 44 subjects (22 subjects with PFPS and 22 healthy controls), aged 18-35 years.
The study will measure hip abductor muscle strength (Peak torque, Maximal total work) using the Biodex Isokinetic System 4 PRO and muscle activity (%MVC) of the gluteus medius, gluteus maximus, and tensor fascia lata using Surface EMG (Noraxon Ultium EMG).
Measurements will be taken in both standing and side-lying positions.
Study Type
Observational
Enrollment (Estimated)
44
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: MOHAMED GOUDA MOHAMED, bachelor of physical therapy
- Phone Number: +201092948701
- Email: mohamed.gouda@acu.edu.eg
Study Locations
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Giza, Egypt
- Ahram Canadian University
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Contact:
- Mohamed Gouda
- Phone Number: +20 10 92948701
- Email: mohamed.gouda@acu.edu.eg
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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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
44 subjects, divided into 22 subjects with PFPS and 22 healthy controls, recruited from the outpatient clinics and staff/students of Ahram Canadian University
Description
Inclusion Criteria:
- Age 18-35 years; Normal BMI; Subjects in the PFPS group diagnosed with unilateral PFPS by an orthopedist; Healthy individuals without knee pain (for the control group)
Exclusion Criteria:
- History of lower limb surgery; Any neurological disorders; Musculoskeletal disorders affecting the lower limb; Additional sources of anterior knee pain (tendonitis, Osgood-Schlatter, bursitis, etc.); Any inflammatory diseases
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
Cohorts and Interventions
Group / Cohort |
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PFPS Group
Subjects with unilateral PFPS diagnosed by an orthopedist; age 18-35 years; normal BMI
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Control Group
Healthy individuals without knee pain; age 18-35 years; normal BMI
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Muscle activity (%MVC) of the gluteus medius, gluteus maximus, and tensor fascia lata
Time Frame: During the assessment procedure (single time point)
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using SEMG
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During the assessment procedure (single time point)
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Peak torque (Nm) of hip abductors muscles
Time Frame: During the assessment procedure (single time point)
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using isokinetic
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During the assessment procedure (single time point)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Maximal total work (J) during concentric and eccentric contractions
Time Frame: During the assessment procedure (single time point)
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Using Isokinetic
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During the assessment procedure (single time point)
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The Arabic Version of the Kujala Score (Anterior Knee Pain Scale)
Time Frame: Baseline/Pre-assessment
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A questionnaire
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Baseline/Pre-assessment
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: mohamed gouda mohamed, bachelor of physical therapy, Teaching assistant, Department of Physiotherapy, Department of Physical Therapy for Musculoskeletal Disorders and its Surgery, Faculty of Physical Therapy, Ahram Canadian University, Giza, Egypt
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Estimated)
December 15, 2025
Primary Completion (Estimated)
January 15, 2026
Study Completion (Estimated)
February 15, 2026
Study Registration Dates
First Submitted
December 13, 2025
First Submitted That Met QC Criteria
December 13, 2025
First Posted (Actual)
December 26, 2025
Study Record Updates
Last Update Posted (Actual)
December 26, 2025
Last Update Submitted That Met QC Criteria
December 13, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cairo University (Other Identifier: Cairo University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
no specific reason
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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