- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07542236
Effects of Hip and Ankle Mobility Rehabilitation in Male Collegiate Athletes With Patellofemoral Pain
Effects of a Hip- and Ankle-Mobility-Based Rehabilitation Program on Pain, Neuromuscular Coordination, and Physical Performance in Soccer Players With Patellofemoral Pain: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Patellofemoral pain is one of the most common overuse-related knee problems in soccer players and is often associated with pain during running, squatting, stair ambulation, jumping, landing, and other load-bearing activities. In addition to pain, patellofemoral pain may impair movement control, neuromuscular function, and lower-limb performance. Increasing evidence suggests that patellofemoral pain should not be viewed only as a local knee disorder, but also in relation to proximal and distal dysfunction within the lower-limb kinetic chain. Restricted hip mobility may alter pelvic and femoral motion during functional tasks, whereas limited ankle dorsiflexion may affect shock absorption, tibial progression, and movement strategy during squatting, landing, deceleration, and change-of-direction tasks. Therefore, improving hip and ankle mobility may represent a clinically relevant rehabilitation strategy for soccer players with patellofemoral pain.
This study uses a randomized, assessor-blinded, parallel-group design to examine the effects of a hip- and ankle-mobility-based rehabilitation program in male soccer players with patellofemoral pain. A total of 48 participants are allocated in a 1:1 ratio to either an intervention group or a control group. The intervention group performs a 6-week rehabilitation program focused on hip internal and external rotation mobility, ankle dorsiflexion mobility, and integrated lower-limb movement exercises, 3 times per week for approximately 30 minutes per session, while continuing regular soccer training. The control group continues regular soccer training without additional structured hip or ankle mobility intervention.
The primary outcomes are pain intensity assessed by visual analog scale and knee-related function assessed by Kujala score. Secondary outcomes include hip internal rotation range of motion, hip external rotation range of motion, weight-bearing ankle dorsiflexion, vastus medialis-vastus lateralis onset timing during a standardized bilateral squat task, Y-Balance Test composite score, and countermovement jump height. Assessments are performed at baseline and after the 6-week intervention. The purpose of the study is to determine whether a mobility-oriented rehabilitation approach can improve both clinical outcomes and functional performance-related measures in soccer players with patellofemoral pain.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Shaanxi
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Xi'an, Shaanxi, China, 710068
- Xi'an Physical Education University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male soccer players aged 18 to 25 years At least 3 years of systematic soccer training experience Currently participating in organized soccer training at least 3 times per week Peripatellar or retropatellar pain consistent with patellofemoral pain Pain provoked during at least one load-bearing knee-flexion activity, including squatting, stair ambulation, running, jumping, or prolonged sitting Patellofemoral pain reproducible during squatting Symptom duration of at least 4 weeks Able to complete all testing and intervention procedures
Exclusion Criteria:
- History of knee surgery or major lower-limb surgery Acute lower-limb injury within the previous 6 months Other diagnoses that could explain anterior knee pain, including ligament injury, meniscal injury, patellar instability, osteoarthritis, or other tibiofemoral pathology Neurological or systemic disease affecting exercise performance Current participation in other structured lower-limb rehabilitation interventions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Hip- and Ankle-Mobility-Based Rehabilitation
Participants receive a 6-week hip- and ankle-mobility-based rehabilitation program, performed 3 times per week for approximately 30 minutes per session, in addition to regular soccer training.
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A 6-week rehabilitation program performed 3 times per week for approximately 30 minutes per session.
The program includes standardized warm-up, hip mobility training, ankle mobility training, and integrated movement exercises designed to improve hip internal and external rotation mobility, ankle dorsiflexion, and lower-limb movement control in soccer players with patellofemoral pain.
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No Intervention: Control
Participants continue regular soccer training during the same 6-week period and do not receive any additional structured hip or ankle mobility intervention.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity assessed by Visual Analog Scale (VAS)
Time Frame: Baseline and 6 weeks
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Average anterior knee pain related to patellofemoral pain assessed using a 10-cm visual analog scale.
Higher scores indicate greater pain intensity.
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Baseline and 6 weeks
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Knee-related function assessed by Kujala score
Time Frame: Baseline and 6 weeks
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Knee-related function assessed using the Kujala Anterior Knee Pain Scale.
Higher scores indicate better knee-related function.
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Baseline and 6 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hip internal rotation range of motion
Time Frame: Baseline and 6 weeks
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Hip internal rotation range of motion measured in degrees using a standard goniometer.
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Baseline and 6 weeks
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Hip external rotation range of motion
Time Frame: Baseline and 6 weeks
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Hip external rotation range of motion measured in degrees using a standard goniometer.
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Baseline and 6 weeks
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Weight-bearing ankle dorsiflexion assessed by weight-bearing lunge test
Time Frame: Baseline and 6 weeks
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Weight-bearing ankle dorsiflexion measured as the maximum toe-to-wall distance in centimeters during the weight-bearing lunge test.
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Baseline and 6 weeks
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Vastus medialis-vastus lateralis onset timing
Time Frame: Baseline and 6 weeks
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Relative onset timing difference between vastus medialis and vastus lateralis measured during a standardized bilateral squat task using surface electromyography.
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Baseline and 6 weeks
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Y-Balance Test composite score
Time Frame: Baseline and 6 weeks
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Dynamic balance performance assessed using the Y-Balance Test composite score.
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Baseline and 6 weeks
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Countermovement jump height
Time Frame: Baseline and 6 weeks
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Lower-limb performance assessed by countermovement jump height measured using a force platform.
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Baseline and 6 weeks
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Collaborators and Investigators
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- XAIPE-PFP-2025-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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.
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