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Rehabilitation for ataxia study: protocol for a randomised controlled trial of an outpatient and supported home-based physiotherapy programme for people with hereditary cerebellar ataxia.
Milne, Sarah C; Corben, Louise A; Roberts, Melissa; Szmulewicz, David; Burns, J; Grobler, Anneke C; Williams, Shannon; Chua, Jillian; Liang, Christina; Lamont, Phillipa J; Grootendorst, Alison C; Massey, Libby; Sue, Carolyn; Dalziel, Kim; LaGrappe, Desiree; Willis, Liz; Freijah, Aleka; Gerken, Paul; Delatycki, Martin B.
Afiliação
  • Milne SC; Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Corben LA; Physiotherapy Department, Monash Health, Cheltenham, Victoria, Australia.
  • Roberts M; School of Primary and Allied Health Care, Monash University, Frankston, Victoria, Australia.
  • Szmulewicz D; Department of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.
  • Burns J; Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Grobler AC; School of Primary and Allied Health Care, Monash University, Frankston, Victoria, Australia.
  • Williams S; Department of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.
  • Chua J; Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Liang C; Physiotherapy Department, Monash Health, Cheltenham, Victoria, Australia.
  • Lamont PJ; Balance Disorders & Ataxia Service, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia.
  • Grootendorst AC; Cerebellar Ataxia Clinic, Alfred Health, Caulfield, Victoria, Australia.
  • Massey L; Monash Medical Centre, Monash Health, Clayton, Victoria, Australia.
  • Sue C; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
  • Dalziel K; University of Sydney School of Health Sciences, Faculty of Medicine and Health & Children's Hospital at Westmead, Sydney, New South Wales, Australia.
  • LaGrappe D; Department of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia.
  • Willis L; Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Freijah A; Physiotherapy Department, Royal Perth Hospital, Perth, Western Australia, Australia.
  • Gerken P; Physiotherapy Department, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Delatycki MB; Physiotherapy Department, Ryde Hospital, Eastwood, New South Wales, Australia.
BMJ Open ; 10(12): e040230, 2020 12 17.
Article em En | MEDLINE | ID: mdl-33334834
INTRODUCTION: Emerging evidence indicates that rehabilitation can improve ataxia, mobility and independence in everyday activities in individuals with hereditary cerebellar ataxia. However, with the rarity of the genetic ataxias and known recruitment challenges in rehabilitation trials, most studies have been underpowered, non-randomised or non-controlled. This study will be the first, appropriately powered randomised controlled trial to examine the efficacy of an outpatient and home-based rehabilitation programme on improving motor function for individuals with hereditary cerebellar ataxia. METHODS AND ANALYSIS: This randomised, single-blind, parallel group trial will compare a 30-week rehabilitation programme to standard care in individuals with hereditary cerebellar ataxia. Eighty individuals with a hereditary cerebellar ataxia, aged 15 years and above, will be recruited. The rehabilitation programme will include 6 weeks of outpatient land and aquatic physiotherapy followed immediately by a 24- week home exercise programme supported with fortnightly physiotherapy sessions. Participants in the standard care group will be asked to continue their usual physical activity. The primary outcome will be the motor domain of the Functional Independence Measure. Secondary outcomes will measure the motor impairment related to ataxia, balance, quality of life and cost-effectiveness. Outcomes will be administered at baseline, 7 weeks, 18 weeks and 30 weeks by a physiotherapist blinded to group allocation. A repeated measures mixed-effects linear regression model will be used to analyse the effect of the treatment group for each of the dependent continuous variables. The primary efficacy analysis will follow the intention-to-treat principle. ETHICS AND DISSEMINATION: The study has been approved by the Monash Health Human Research Ethics Committee (HREC/18/MonH/418) and the Human Research Ethics Committee of the Northern Territory Department of Health and Menzies School of Health Research (2019/3503). Results will be published in peer-reviewed journals, presented at national and/or international conferences and disseminated to Australian ataxia support groups. TRIAL REGISTRATION NUMBER: ACTRN12618000908235.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pacientes Ambulatoriais / Qualidade de Vida / Ataxia Cerebelar / Modalidades de Fisioterapia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pacientes Ambulatoriais / Qualidade de Vida / Ataxia Cerebelar / Modalidades de Fisioterapia Idioma: En Ano de publicação: 2020 Tipo de documento: Article