Patellofemoral Pain Syndrome Clinical Trial
Official title:
Foot Orthotics in the Treatment of Patellofemoral Pain Syndrome: A Randomised Clinical Trial in Primary Care
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.
Status | Completed |
Enrollment | 176 |
Est. completion date | June 2007 |
Est. primary completion date | June 2007 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 40 Years |
Eligibility |
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 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Australia | Musculoskeletal Pain & Injury Research Unit, Division of Physiotherapy, The University of Queensland | Brisbane | Queensland |
Lead Sponsor | Collaborator |
---|---|
The University of Queensland | National Health and Medical Research Council, Australia |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Worst and Usual Pain Visual Analogue Scale | |||
Primary | Functional Index Questionnaire | |||
Primary | Anterior Knee Pain Scale | |||
Primary | Patient Perceived Treatment Effect score | |||
Primary | Perceived Global Effect 5 Point Scale | |||
Secondary | Physical activity level in previous week | |||
Secondary | Step up, step down and squat tests | |||
Secondary | Lower Extremity Functional Scale | |||
Secondary | McGill Pain Questionnaire | |||
Secondary | SF-36 Health Survey | |||
Secondary | Hospital Anxiety and Depression Scale | |||
Secondary | Patient Specific Functional Scale | |||
Secondary | Pressure pain threshold |
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