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Treatment of anterior knee pain according to risk factor correction

Comparing two treatments of pattelofemoral pain syndrome, routin approch and based on risk factors according to pain and function, among patients visited in sport medicine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201010305050N1
Enrollment
60
Registered
2011-04-14
Start date
2011-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Patellofemoral pain syndrome. Patellofemoral disorders

Interventions

Intervention 1: group A: regardless of risk factors, routin treatment that includes perscription of narcotic drugs and quadriceps isometric exercise is done 3 times per day with 8 repitition each time
Rehabilitation
group A: regardless of risk factors, routin treatment that includes perscription of narcotic drugs and quadriceps isometric exercise is done 3 times per day with 8 repitition each time holding for 10-
group B: In addition to treatments in group A, receive treatment and correction of found risk factors in physical exam including: 1-appropriate shoes and insoles for pess planus or pess cavus 2-heel l

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: having at least 3 of these signs/symptoms: 1.pain during stair climbing or squat exercise, running, cycling, long sitting in bending knee position 2.patellar grinding 3.positive physical tests. Exclusion criteria are any history of knee trauma or operation, history of rheumatologic disease, history of knee osteoarthritis and any interventional treartment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: at begining of study and 3month later. Method of measurement: questioner.;Function. Timepoint: at begining of study and 3 months later. Method of measurement: Kujala Function Score Questionnaire.

Secondary

MeasureTime frame
EMG changing. Timepoint: at begening and 3 months later. Method of measurement: surface EMG.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Zahra Hamedi

Tehran university of medical sciences

hamedi@razi.tums.ac.ir+98 21 8863 0227

Outcome results

None listed

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