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Effectiveness of gait retraining for patients with patellofemoral pain

Effectiveness of gait retraining for patients with patellofemoral pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078289
Enrollment
Unknown
Registered
2023-12-04
Start date
2023-12-04
Completion date
Unknown
Last updated
2023-12-10

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

Conditions

Patellofemoral joint pain syndrome

Interventions

Intervention group:gait retraining

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) 18-40 years of age; (2) unilateral anterior knee pain over 4 weeks ; (3) insidious onset of symptoms unrelated to traumatic accident; (4) presence of pain in any two following activities: running, jumping, squat ting, kneeling, upstairs/downstairs or prolonged sitting; and (5) presence of two signs in following examiniations: pain during apprehension test, pain during patellar compression test, crepitation during the compression test, tenderness upon palpation of the posterior surface of the patella or surrounding structures, and pain during resisted knee extension.

Exclusion criteria

Exclusion criteria: (1) history of patellar dislocation or subluxation, chondral damage, or ligament laxity; (2) suspicion of patellar tendinopathy, localized pain on patellar tendon and relieved pain during knee resisted extension; (3) previous knee surgery or arthritis; (4) any other invasive procedure in the affected knee, including arthroscopy or intra-articular injection in the past 12 months; (5) history of physical therapy or a strengthening procedure of the affected knee in the past 6 months; (6) received nonsteroidal anti-inflammatory drugs (NSAIDs) in the past 3 months; (7) any neurological, heart, or vascular disease, such as blood coagulation disorders; (8) abnormal blood pressure (resting systolic blood pressure [SBP] > 140 or diastolic blood pressure [DBP] > 90 mmHg); (9) other acute or chronic disorders or psychiatric conditions that will affect physical or cognitive functions; (10) pregnancy.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
AKPS;Running biomechanical evaluation;

Countries

China

Contacts

Public ContactHaonan Wang

Beijing Sport University

wanghaonan@bsu.edu.cn+86 156 0056 3019

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026