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Gait Retraining for Runners With Patellofemoral Pain

Gait Retraining Intervention for Female Runners With Patellofemoral Pain: Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07557797
Enrollment
44
Registered
2026-04-29
Start date
2026-05-15
Completion date
2026-12-15
Last updated
2026-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patellofemoral Pain, PFP

Keywords

Patellofemoral pain, gait retraining, runner

Brief summary

Patellofemoral pain (PFP) is a common overuse injury in runners. Increased patellofemoral joint stress (PFJS) is an important biomechanical factor associated with PFP. Gait retraining, especially cadence modification, may reduce PFJS and improve symptoms, but evidence from randomized controlled trials remains limited. This study investigated whether wearable device-assisted gait retraining was more effective than education alone in reducing pain, improving function, and altering running biomechanics in female runners with PFP.

Interventions

BEHAVIORALGait retraining

The intervention is a wearable device-assisted gait retraining program (home) designed specifically for female runners with patellofemoral pain.

BEHAVIORALEducation

PFP education, load management strategies, symptom-based training modifications, and strengthening exercises

Sponsors

Beijing Sport University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Female, Age 18-45 years * Unilateral/bilateral anterior knee pain \> 4 weeks * VAS pain ≥ 3/10 during running and ≥ 2 of the following: jumping, squatting, kneeling, stairs, prolonged sitting, or resisted knee extension * Running ≥ 15 km per week * Natural rearfoot striker

Exclusion criteria

* Acute trauma, history of patellar dislocation, meniscal/chondral lesions * Prior knee surgery or injection in past 12 months * Rheumatologic, neurologic, or degenerative disease * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Visual Analogue Scale for Pain during runningBaseline, Week 6, Week 18The Visual Analogue Scale (VAS) is a validated, widely used instrument for assessing subjective pain intensity. It consists of a 10-centimeter horizontal line, with one end (0) representing "no pain" and the other end (10) representing "worst imaginable pain." It will be evaluated during running.

Secondary

MeasureTime frameDescription
Visual Analogue Scale for usual painBaseline, Week 6, Week 18The Visual Analogue Scale (VAS) is a validated, widely used instrument for assessing subjective pain intensity. It consists of a 10-centimeter horizontal line, with one end (0) representing "no pain" and the other end (10) representing "worst imaginable pain." It will be evaluated for usual pain.
Anterior Knee Pain ScaleBaseline, Week 6, Week 18The Anterior Knee Pain Scale (AKPS), also referred to as the Kujala Score, is a patient-reported outcome measure designed to evaluate symptoms and functional limitations associated with anterior knee pain and patellofemoral disorders. It consists of 13 items covering domains such as pain during various activities (e.g., walking, running, jumping, climbing stairs, squatting), functional limitations, abnormal gait, muscle atrophy, and difficulty with prolonged sitting. Each item is scored on an ordinal scale, and the total score ranges from 0 to 100, with higher scores indicating better knee function and fewer symptoms.
Knee Flexion AngleBaseline, Week 6Peak knee flexion angle will be assessed during running trials using a 3-dimensional motion capture system. Reflective markers will be placed according to a standard lower-limb biomechanical model.
Ground Reaction ForceBaseline, Week 6Ground reaction force (GRF) will be measured during overground running using embedded force plates synchronized with motion capture.
Visual Analogue Scale for the worst painBaseline, Week 6, Week 18The Visual Analogue Scale (VAS) is a validated, widely used instrument for assessing subjective pain intensity. It consists of a 10-centimeter horizontal line, with one end (0) representing "no pain" and the other end (10) representing "worst imaginable pain." It will be evaluated for the worst pain.

Countries

China

Contacts

CONTACTHaonan Wang
wanghaonan@bsu.edu.cn8615600563019
PRINCIPAL_INVESTIGATORHaonan Wang

Beijing Sport University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026