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A Clinical Study in the Use of Orthotics in Treating Pain in the Front of the Knee
This study is currently recruiting participants.
Verified by The University of Queensland, July 2005
Sponsors and Collaborators: The University of Queensland
National Health and Medical Research Council, Australia
Information provided by: The University of Queensland
ClinicalTrials.gov Identifier: NCT00118521
  Purpose

Musculoskeletal conditions account for the third leading cause of health systems expenditure in Australia. Patellofemoral pain syndrome or pain about the knee cap is such a condition often treated in primary care. Both the individual and community are affected by this condition with an estimated 1 in 4 sufferers having problems and pain up to 20 years after first being afflicted. Importantly, it interferes with activities such as walking, jogging, gym classes and aerobics, which are often prescribed to prevent serious conditions of the heart, diabetes and obesity. Hence, it negatively impacts the health and well being of our nation.

Two popular treatment options that are commonly prescribed for the management of patellofemoral pain syndrome are physiotherapy and foot orthotics. To date, there is some evidence supporting physiotherapy, especially current best practice methods, such as a combined program of therapeutic exercise, manual therapy and kneecap taping. There is a lack of evidence for the use of orthotics in treating patellofemoral pain syndrome.

This project will conduct a randomised clinical trial to evaluate the relative benefits of orthotics as the sole treatment of patellofemoral pain syndrome and also when combined with physiotherapy. Factors associated with predicting the results of orthotic therapy will be studied to see if there are any tests that a health care practitioner can perform to provide information early on in a consultation regarding possible treatment outcomes. A cost-benefit analysis will also be conducted to calculate the relative economic merits of the treatments.

A tangible outcome of this project will be the development of clinical guidelines for the most effective method of treating patellofemoral pain syndrome in primary health care.


Condition Intervention Phase
Patellofemoral Pain Syndrome
Procedure: Foot Orthotics
Procedure: Physiotherapy
Phase III

MedlinePlus related topics: Foot Health
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: Foot Orthotics in the Treatment of Patellofemoral Pain Syndrome: A Randomised Clinical Trial in Primary Care

Further study details as provided by The University of Queensland:

Primary Outcome Measures:
  • Worst and Usual Pain Visual Analogue Scale
  • Functional Index Questionnaire
  • Anterior Knee Pain Scale
  • Patient Perceived Treatment Effect score
  • Perceived Global Effect 5 Point Scale

Secondary Outcome Measures:
  • Physical activity level in previous week
  • Step up, step down and squat tests
  • Lower Extremity Functional Scale
  • McGill Pain Questionnaire
  • SF-36 Health Survey
  • Hospital Anxiety and Depression Scale
  • Patient Specific Functional Scale
  • Pressure pain threshold

Estimated Enrollment: 176
Study Start Date: May 2004
Estimated Study Completion Date: July 2007
Detailed Description:

Musculoskeletal conditions account for the third leading cause of health systems expenditure in Australia. Patellofemoral pain syndrome or pain about the knee cap is such a condition often treated in primary care. Both the individual and community are affected by this condition with an estimated 1 in 4 sufferers having problems and pain up to 20 years after first being afflicted. Importantly, it interferes with activities such as walking, jogging, gym classes and aerobics, which are often prescribed to prevent serious conditions of the heart, diabetes and obesity. Hence, it negatively impacts the health and well being of our nation.

  Eligibility

Ages Eligible for Study:   18 Years to 40 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Clinical diagnosis of patellofemoral pain syndrome (non traumatic origin) of at least 6 weeks duration
  • Pain with at least 2 of the following activities: stair walking, jogging/running, squatting, hopping/jumping, kneeling or prolonged sitting

Exclusion Criteria:

  • Concomitant injury or pathology of other knee joint structures, eg. meniscal, ligamentous etc.
  • Pain in or referred from the lumbar spine and hip
  • History of knee fractures, patellar dislocation/subluxation with a positive apprehension test
  • Prior physiotherapy treatment (including patellar taping) within the past 12 months
  • History of allergic reaction to adhesive tape
  • Current or previous foot orthotic use
  • Any condition of the foot that precludes orthotic therapy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00118521

Contacts
Contact: Bill Vicenzino, PhD 61 7 33652781 b.vicenzino@uq.edu.au

Locations
Australia, Queensland
Musculoskeletal Pain & Injury Research Unit, Division of Physiotherapy, The University of Queensland Recruiting
Brisbane, Queensland, Australia, 4072
Contact: Bill Vicenzino, PhD     61-7-33652781     b.vicenzino@uq.edu.au    
Principal Investigator: Bill Vicenzino, PhD            
Sponsors and Collaborators
The University of Queensland
National Health and Medical Research Council, Australia
Investigators
Principal Investigator: Bill Vicenzino, PhD The University of Queensland
  More Information

Publications indexed to this study:
Study ID Numbers: 2003001023NHMRC, NHMRC#301037
Study First Received: July 1, 2005
Last Updated: February 1, 2006
ClinicalTrials.gov Identifier: NCT00118521  
Health Authority: Australia: Human Research Ethics Committee

Keywords provided by The University of Queensland:
Anterior Knee Pain

Study placed in the following topic categories:
Musculoskeletal Diseases
Joint Diseases
Patellofemoral Pain Syndrome
Pain

Additional relevant MeSH terms:
Pathologic Processes
Disease
Syndrome

ClinicalTrials.gov processed this record on February 10, 2009