Effects of Hip and Ankle Mobility Rehabilitation in Male Collegiate Athletes With Patellofemoral Pain

April 26, 2026 updated by: Yue Dou, Beijing Sport University

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

This study evaluates whether a 6-week hip- and ankle-mobility-based rehabilitation program can improve pain, knee-related function, neuromuscular coordination, and physical performance in male soccer players with patellofemoral pain. Patellofemoral pain is a common condition in soccer players and may affect training tolerance, movement control, and sports performance. In this randomized controlled trial, participants are assigned to either an intervention group receiving hip- and ankle-mobility-based rehabilitation in addition to regular soccer training or a control group continuing regular soccer training alone. The rehabilitation program is performed 3 times per week for 6 weeks. Main outcomes include pain intensity and knee-related function. Additional outcomes include hip and ankle range of motion, vastus medialis-vastus lateralis onset timing, Y-Balance Test performance, and countermovement jump height. This study aims to determine whether improving proximal and distal joint mobility can contribute to better clinical and functional recovery in soccer players with patellofemoral pain.

Study Overview

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

Interventional

Enrollment (Actual)

48

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

    • Shaanxi
      • Xi'an, Shaanxi, China, 710068
        • Xi'an Physical Education 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

  • Adult

Accepts Healthy Volunteers

No

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

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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.
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.
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.

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
Average anterior knee pain related to patellofemoral pain assessed using a 10-cm visual analog scale. Higher scores indicate greater pain intensity.
Baseline and 6 weeks
Knee-related function assessed by Kujala score
Time Frame: Baseline and 6 weeks
Knee-related function assessed using the Kujala Anterior Knee Pain Scale. Higher scores indicate better knee-related function.
Baseline and 6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hip internal rotation range of motion
Time Frame: Baseline and 6 weeks
Hip internal rotation range of motion measured in degrees using a standard goniometer.
Baseline and 6 weeks
Hip external rotation range of motion
Time Frame: Baseline and 6 weeks
Hip external rotation range of motion measured in degrees using a standard goniometer.
Baseline and 6 weeks
Weight-bearing ankle dorsiflexion assessed by weight-bearing lunge test
Time Frame: Baseline and 6 weeks
Weight-bearing ankle dorsiflexion measured as the maximum toe-to-wall distance in centimeters during the weight-bearing lunge test.
Baseline and 6 weeks
Vastus medialis-vastus lateralis onset timing
Time Frame: Baseline and 6 weeks
Relative onset timing difference between vastus medialis and vastus lateralis measured during a standardized bilateral squat task using surface electromyography.
Baseline and 6 weeks
Y-Balance Test composite score
Time Frame: Baseline and 6 weeks
Dynamic balance performance assessed using the Y-Balance Test composite score.
Baseline and 6 weeks
Countermovement jump height
Time Frame: Baseline and 6 weeks
Lower-limb performance assessed by countermovement jump height measured using a force platform.
Baseline and 6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Actual)

January 15, 2026

Primary Completion (Actual)

March 2, 2026

Study Completion (Actual)

March 4, 2026

Study Registration Dates

First Submitted

April 14, 2026

First Submitted That Met QC Criteria

April 14, 2026

First Posted (Actual)

April 21, 2026

Study Record Updates

Last Update Posted (Actual)

April 30, 2026

Last Update Submitted That Met QC Criteria

April 26, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

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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