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Comparison of the effect of a course of corrective exercises with and without foot orthosis on people with patellofemoral pain syndrome.

comparison of the effect of a course of course of corrective exercises with and without foot orthosis on the improvement of pain and performance of patients with patellofemoral pain syndrome.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230604058380N1
Enrollment
117
Registered
2023-07-28
Start date
2023-08-21
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Patellofemoral pain syndrome.

Interventions

Intervention 1: Intervention group: Intervention group: The first intervention group receives proximal hip and core strengthening exercises for eight weeks. Intervention 2: Intervention group: The sec

Sponsors

University of guilan
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age range between 18 and 40 years Having knee pain for at least 6 weeks or more Having anterior knee pain with non-traumatic origin Not having a history of injury and surgery on the spine and lower limbs Exacerbation of pain with at least 2 of the following activities including: running, jumping, walking on a hill or stairs, sitting for a long time, kneeling, squatting Clark's test is positive Navicular drop more than 9 mm A score greater than 6 from the foot posture index Pain score greater than 3 on the visual analog scale

Exclusion criteria

Exclusion criteria: Knee meniscus and ligament or tendon injury patellar dislocation (patellar instability) Osgoodschlatter disease Celica syndrome, Larsen-Johnson syndrom knee joint effusion

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pain measurement before and after exercises and intervention. Method of measurement: Visual Analog Scale (VAS).

Secondary

MeasureTime frame
Disability. Timepoint: Measurement of functional before and after exercises and intervention. Method of measurement: Kujala questionnaire.;Balance. Timepoint: Measurement of functional before and after exercises and intervention. Method of measurement: Y balance test.;Functional. Timepoint: Measurement of functional before and after exercises and intervention. Method of measurement: step down test at 30 second.;Functional. Timepoint: Measurement of functional before and after exercises and intervention. Method of measurement: Single leg squat test.;Functional. Timepoint: Measurement of functional before and after exercises and intervention. Method of measurement: bilateral squat test.;Q angle. Timepoint: Measurement of Q angle before and after exercises and intervention. Method of measurement: Measuring the angle Q with a goniometer.;Flat foot. Timepoint: Measurement before and after exercises and intervention. Method of measurement: Navicular drop.;Quality of life. Timepoint: Measurement before and after exercises and intervention. Method of measurement: Quality of life questionnaire (SF_36).;Functional. Timepoint: Measurement of functional before and after exercises and intervention. Method of measurement: anteromidial lunge test.;Disability. Timepoint: Measurement disability of before and after exercises and intervention. Method of measurement: Kujala questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmansoureh barati ashtiani

Gilan University

manbarati1377@gmail.com+98 903 499 0769

Outcome results

None listed

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