Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/52464
Title: Efficacy of arch contouring foot orthoses for midfoot osteoarthritis: Protocol for a randomised controlled trial.
Authors: Lim P.Q.X.;Menz H.B.;Landorf K.B.;Kaminski M.R.;Buldt A.K.;Lithgow M.J.;Paterson K.L.;Halstead J.;Munteanu S.E.
Monash Health Department(s): Podiatry
Allied Health
Institution: (Lim, Menz, Landorf, Kaminski, Buldt, Lithgow, Munteanu) Discipline of Podiatry, School of Allied Health, Human Services and Sport, La Trobe University, Melbourne, VIC, Australia
(Kaminski) Department of Podiatry, Monash Health, Melbourne, VIC, Australia
(Kaminski) School of Primary and Allied Health Care, Monash University, Melbourne, VIC, Australia
(Paterson) Department of Physiotherapy, Centre for Health, Exercise and Sports Medicine, School of Health Sciences, University of Melbourne, Melbourne, VIC, Australia
(Halstead) University of Leeds, NIHR Leeds Biomedical Research Centre, Leeds Community Healthcare NHS Trust, Leeds, United Kingdom
Issue Date: 9-Sep-2024
Copyright year: 2024
Place of publication: United States
Publication information: Journal of Foot and Ankle Research. 17(3) (pp e70000), 2024. Date of Publication: 01 Sep 2024.
Journal: Journal of Foot and Ankle Research
Abstract: INTRODUCTION: Midfoot osteoarthritis (OA) is a painful and disabling condition. Arch contouring foot orthoses have been recommended for midfoot OA, yet there is no high-quality evidence from randomised controlled trials to support their use. This clinical trial aims to evaluate the efficacy of arch contouring foot orthoses for midfoot OA. METHOD(S): This will be a parallel-group randomised controlled superiority trial. One-hundred and forty community-dwelling people with painful midfoot OA will be randomised to receive either arch contouring foot orthoses or flat sham inserts. Outcome measures will be obtained at baseline, 4, 8 and 12 weeks; the primary endpoint for assessing efficacy being 12 weeks. The primary outcome measure will be average midfoot pain whilst walking over the last 7 days on an 11-point numerical rating scale. Secondary outcome measures include function (walking/standing subscale of the Manchester-Oxford Foot Questionnaire), participants' perception of overall treatment effect (self-reported global rating of change on a 15-point Likert scale), physical activity (Incidental and Planned Exercise Questionnaire), general health-related quality of life (Short Form-12 Version 2.0), use of co-interventions and adverse events. DISCUSSION: This trial will evaluate the efficacy of arch contouring foot orthoses for relieving pain and improving function, physical activity and health-related quality of life in people with midfoot OA. The findings will provide high-quality evidence as to whether arch contouring foot orthoses are efficacious and will help to inform clinical guidelines about the use of foot orthoses for midfoot OA. TRIAL REGISTRATION: Australian and New Zealand Clinical Trial Registry (ACTRN12623000953639).Copyright © 2024 The Author(s). Journal of Foot and Ankle Research published by John Wiley & Sons Australia, Ltd on behalf of Australian Podiatry Association and The Royal College of Podiatry.
DOI: http://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1002/jfa2.70000
PubMed URL: 39223075 [https://www.ncbi.nlm.nih.gov/pubmed/?term=39223075]
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/52464
Type: Article
Subjects: foot orthosis
middle osteoarthritis
rehabilitation
Type of Clinical Study or Trial: Randomised controlled trial
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