Abstract

BackgroundPatellofemoral pain syndrome is a highly prevalent musculoskeletal overuse condition that has a significant impact on participation in daily and physical activities. A recent systematic review highlighted the lack of high quality evidence from randomised controlled trials for the conservative management of patellofemoral pain syndrome. Although foot orthoses are a commonly used intervention for patellofemoral pain syndrome, only two pilot studies with short term follow up have been conducted into their clinical efficacy.Methods/designA randomised single-blinded clinical trial will be conducted to investigate the clinical efficacy and cost effectiveness of foot orthoses in the management of patellofemoral pain syndrome. One hundred and seventy-six participants aged 18–40 with anterior or retropatellar knee pain of non-traumatic origin and at least six weeks duration will be recruited from the greater Brisbane area in Queensland, Australia through print, radio and television advertising. Suitable participants will be randomly allocated to receive either foot orthoses, flat insoles, physiotherapy or a combined intervention of foot orthoses and physiotherapy, and will attend six visits with a physiotherapist over a 6 week period. Outcome will be measured at 6, 12 and 52 weeks using primary outcome measures of usual and worst pain visual analogue scale, patient perceived treatment effect, perceived global effect, the Functional Index Questionnaire, and the Anterior Knee Pain Scale. Secondary outcome measures will include the Lower Extremity Functional Scale, McGill Pain Questionnaire, 36-Item Short-Form Health Survey, Hospital Anxiety and Depression Scale, Patient-Specific Functional Scale, Physical Activity Level in the Previous Week, pressure pain threshold and physical measures of step and squat tests. Cost-effectiveness analysis will be based on treatment effectiveness against resource usage recorded in treatment logs and self-reported diaries.DiscussionThe randomised clinical trial will utilise high-quality methodologies in accordance with CONSORT guidelines, in order to contribute to the limited knowledge base regarding the clinical efficacy of foot orthoses in the management of patellofemoral pain syndrome, and provide practitioners with high-quality evidence upon which to base clinical decisions.Trial registrationAustralian Clinical Trials Registry ACTRN012605000463673ClinicalTrials.gov NCT00118521

Highlights

  • Patellofemoral pain syndrome is a highly prevalent musculoskeletal overuse condition that has a significant impact on participation in daily and physical activities

  • Patellofemoral pain syndrome (PFP) is a distinct clinical entity defined as "idiopathic pain arising from the anterior knee/patellofemoral region that is of otherwise unknown origin" [1]

  • As regular physical activity is highly recommended for the prevention of conditions such as cardiovascular disease and type II diabetes, PFP may have important implications for the long term health of affected individuals

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Summary

Discussion

In order to determine the clinical efficacy and cost-effectiveness of foot orthoses in the management of PFP, a pragmatic randomised clinical trial is to be conducted. As recommended by the CONSORT group [6], the RCT design has endeavoured to utilise outcome measures that have established reliability and validity and, where possible, have been used previously in PFP participants. This enhances the quality of the measurement and outcomes, and facilitates direct comparisons with other studies that have investigated interventions for PFP and possible meta-analyses in the future. It is anticipated that findings from this study will contribute to the limited knowledge base regarding the clinical efficacy of foot orthoses in the management of PFP, and provide clinicians with high-quality evidence upon which to base clinical decision making

Background
Methods
Australian Acute Musculoskeletal Pain Guidelines Group
26. Pontinen PJ
Findings
37. Subotnik SI
Full Text
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