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Targeted Intervention in Patellofemoral Pain Syndrome

Targeted Intervention in Patellofemoral Pain Syndrome - Targeted treatment in patient with patellofemoral pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028738
Enrollment
20
Registered
2017-08-18
Start date
2017-09-18
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

patellofemoral pain

Interventions

Clinic based knee exercises and/or electrotherapy modalities 3 times per week, duration: 6 weeks Specific exercises and/or foot orthoses and /or knee orthoses application, 3 times per week, duration:

Sponsors

BASKENT UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Anterior knee pain during at least two following activities; prolonged sitting, climbing stairs, squatting,running, hopping, kneeling 2) Pain during at least two of the followings: manuel compression, palpation of the posterolateral and posteromedial borders of the patella, resistive knee extension

Exclusion criteria

Exclusion criteria: previous knee surgery clinical evidence of ligamentous instability, a history of patellar subluxation or dislocation, joint effusion, locking and/or giving way, bursitis, tendinopathy, Osgood Schlatters disease, Sinding-Larsen Johansson Syndrome, muscle tears or symptomatic knee plicae, serious co-morbidity which would preclude or affect compliance with the assessment, pregnancy.

Design outcomes

Primary

MeasureTime frame
Alterations in Pain and functional capabilities after targeted intervention patient with patellofemoral pain syndrome

Secondary

MeasureTime frame
Alterations in lower extremity stifness, strength, biomechanical parameters after treatment

Countries

Europe

Contacts

Public ContactHayri Baran Yosmaoglu

Baskent University Faculty of Health Science/Department of Physiotherapy

baran79@gmail.com+903122466673

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026