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Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial

BACKGROUND: Knee osteoarthritis (OA) is a leading cause of musculoskeletal pain and disability globally, and abnormal knee loading is central to disease pathogenesis. Clinical guidelines recommend clinicians provide advice regarding appropriate footwear for people with knee OA, yet there is little r...

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Autores principales: Paterson, Kade L., Bennell, Kim L., Wrigley, Tim V., Metcalf, Ben R., Campbell, Penny K., Kazsa, Jessica, Hinman, Rana S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052703/
https://www.ncbi.nlm.nih.gov/pubmed/30021584
http://dx.doi.org/10.1186/s12891-018-2144-1
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author Paterson, Kade L.
Bennell, Kim L.
Wrigley, Tim V.
Metcalf, Ben R.
Campbell, Penny K.
Kazsa, Jessica
Hinman, Rana S.
author_facet Paterson, Kade L.
Bennell, Kim L.
Wrigley, Tim V.
Metcalf, Ben R.
Campbell, Penny K.
Kazsa, Jessica
Hinman, Rana S.
author_sort Paterson, Kade L.
collection PubMed
description BACKGROUND: Knee osteoarthritis (OA) is a leading cause of musculoskeletal pain and disability globally, and abnormal knee loading is central to disease pathogenesis. Clinical guidelines recommend clinicians provide advice regarding appropriate footwear for people with knee OA, yet there is little research comparing the effects of different footwear on knee OA symptoms. Research suggests that wearing flat flexible shoes is associated with lower knee joint loads compared to stable supportive shoe styles. This two-arm pragmatic, comparative effectiveness randomised controlled trial will compare the effects of daily use of flat flexible shoes and stable supportive shoes on knee OA clinical outcomes, over 6 months. METHODS: 164 people with symptomatic medial tibiofemoral OA of moderate to severe radiographic severity (Kellgren and Lawrence Grade 3 & 4) will be recruited from the community. Following baseline assessment, participants will be randomly allocated to receive either i) flat flexible shoes or; ii) stable supportive shoes. Participants will choose two different pairs of shoes from a selection that fulfil the criteria in their allocated shoe class. Limited disclosure will blind participants to group allocation. Participants will be instructed to wear their allocated shoes daily for 6 months (minimum of 6 h/day), after which participants will be reassessed. The primary outcomes are knee pain severity on walking (measured by numerical rating scale) and self-reported physical function (measured by the Western Ontario and McMaster Universities Osteoarthritis Index), assessed at baseline and 6 months. Secondary outcomes include additional measures of knee pain, function, sport and recreation participation and quality-of-life (measured using subscales of the Knee Osteoarthritis Outcome Score), as well as pain at other sites (measured by numerical rating scale), self-reported global ratings of change in pain and physical function (measured by 7-point rating scale), and physical activity levels (measured by Physical Activity Scale for the Elderly). DISCUSSION: This study will determine whether daily wear of flat flexible shoes improves clinical outcomes in the management of knee OA, compared to stable supportive shoes. Findings will assist clinicians in providing evidence-based advice regarding appropriate footwear for people with knee OA to self-manage symptoms. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry reference: ACTRN12617001098325. Registered 28/07/2017.
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spelling pubmed-60527032018-07-23 Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial Paterson, Kade L. Bennell, Kim L. Wrigley, Tim V. Metcalf, Ben R. Campbell, Penny K. Kazsa, Jessica Hinman, Rana S. BMC Musculoskelet Disord Study Protocol BACKGROUND: Knee osteoarthritis (OA) is a leading cause of musculoskeletal pain and disability globally, and abnormal knee loading is central to disease pathogenesis. Clinical guidelines recommend clinicians provide advice regarding appropriate footwear for people with knee OA, yet there is little research comparing the effects of different footwear on knee OA symptoms. Research suggests that wearing flat flexible shoes is associated with lower knee joint loads compared to stable supportive shoe styles. This two-arm pragmatic, comparative effectiveness randomised controlled trial will compare the effects of daily use of flat flexible shoes and stable supportive shoes on knee OA clinical outcomes, over 6 months. METHODS: 164 people with symptomatic medial tibiofemoral OA of moderate to severe radiographic severity (Kellgren and Lawrence Grade 3 & 4) will be recruited from the community. Following baseline assessment, participants will be randomly allocated to receive either i) flat flexible shoes or; ii) stable supportive shoes. Participants will choose two different pairs of shoes from a selection that fulfil the criteria in their allocated shoe class. Limited disclosure will blind participants to group allocation. Participants will be instructed to wear their allocated shoes daily for 6 months (minimum of 6 h/day), after which participants will be reassessed. The primary outcomes are knee pain severity on walking (measured by numerical rating scale) and self-reported physical function (measured by the Western Ontario and McMaster Universities Osteoarthritis Index), assessed at baseline and 6 months. Secondary outcomes include additional measures of knee pain, function, sport and recreation participation and quality-of-life (measured using subscales of the Knee Osteoarthritis Outcome Score), as well as pain at other sites (measured by numerical rating scale), self-reported global ratings of change in pain and physical function (measured by 7-point rating scale), and physical activity levels (measured by Physical Activity Scale for the Elderly). DISCUSSION: This study will determine whether daily wear of flat flexible shoes improves clinical outcomes in the management of knee OA, compared to stable supportive shoes. Findings will assist clinicians in providing evidence-based advice regarding appropriate footwear for people with knee OA to self-manage symptoms. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry reference: ACTRN12617001098325. Registered 28/07/2017. BioMed Central 2018-07-18 /pmc/articles/PMC6052703/ /pubmed/30021584 http://dx.doi.org/10.1186/s12891-018-2144-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Paterson, Kade L.
Bennell, Kim L.
Wrigley, Tim V.
Metcalf, Ben R.
Campbell, Penny K.
Kazsa, Jessica
Hinman, Rana S.
Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial
title Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial
title_full Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial
title_fullStr Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial
title_full_unstemmed Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial
title_short Footwear for self-managing knee osteoarthritis symptoms: protocol for the Footstep randomised controlled trial
title_sort footwear for self-managing knee osteoarthritis symptoms: protocol for the footstep randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052703/
https://www.ncbi.nlm.nih.gov/pubmed/30021584
http://dx.doi.org/10.1186/s12891-018-2144-1
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