A single-blinded, randomized, parallel group superiority trial investigating the effects of footwear and custom foot orthoses versus footwear alone in individuals with patellofemoral joint osteoarthritis: a phase II pilot trial protocol

被引:6
|
作者
Wyndow, Narelle [1 ]
Crossley, Kay M. [2 ]
Vicenzino, Bill [1 ]
Tucker, Kylie [3 ]
Collins, Natalie J. [1 ]
机构
[1] Univ Queensland, Sch Hlth & Rehabil Sci, St Lucia, Qld 4072, Australia
[2] La Trobe Univ, Sch Allied Hlth, Coll Sci Hlth & Engn, Bundoora, Vic 3086, Australia
[3] Univ Queensland, Sch Biomed Sci, St Lucia, Qld 4072, Australia
来源
基金
英国医学研究理事会;
关键词
Randomised controlled trial; Phase II trial; Footwear; Foot orthoses; Patellofemoral; Osteoarthritis; ANTERIOR KNEE PAIN; OUTCOME SCORE KOOS; CLINICAL-TRIAL; MUSCULOSKELETAL PAIN; PHYSIOTHERAPY; PREVALENCE; EFFICACY; THERAPY; HEALTH; SCALE;
D O I
10.1186/s13047-017-0200-y
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Patellofemoral joint osteoarthritis is a common condition, yet information regarding conservative management is lacking. Foot orthoses are an effective intervention for improving pain and function in younger individuals with patellofemoral pain and may be effective in those with patellofemoral osteoarthritis. This pilot study will seek to establish the feasibility of a phase III randomised controlled trial to investigate whether foot orthoses worn in prescribed motion controlled footwear are superior to prescribed motion control footwear alone in the management of patellofemoral osteoarthritis. Methods/design: This phase II pilot clinical trial is designed as a randomized, single-blind, parallel group, two arm, superiority trial. The trial will recruit 44 participants from Queensland and Tasmania, Australia. Volunteers aged 40 years and over must have clinical symptoms and radiographic evidence of patellofemoral osteoarthritis to be eligible for inclusion. Those eligible will be randomized to receive either foot orthoses and prescribed motion control shoes, or prescribed motion control shoes alone, to be worn for a period of 4 months. The feasibility of a phase III clinical trial will be evaluated by assessing factors such as recruitment rate, number of eligible participants, participant compliance with the study protocol, adverse events, and drop-out rate. A secondary aim of the study will be to determine completion rates and calculate effect sizes for patient reported outcome measures such as knee-related symptoms, function, quality of life, kinesiophobia, self-efficacy, general and mental health, and physical activity at 2 and 4 months. Primary outcomes will be reported descriptively while effect sizes and 95% confidence intervals will be calculated for the secondary outcome measures. Data will be analysed using an intention-to-treat principle. Discussion: The results of this pilot trial will help determine the feasibility of a phase III clinical trial investigating whether foot orthoses plus motion control footwear are superior to motion control footwear alone in individuals with patellofemoral osteoarthritis. A Phase III clinical trial will help guide footwear and foot orthoses recommendations in the clinical management of this disorder.
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页数:13
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