Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/26578
Title: 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.
Authors: Delatycki M.B.;Dalziel K.;Lagrappe D.;Willis L.;Freijah A.;Gerken P.;Milne S.C. ;Corben L.A.;Roberts M.;Szmulewicz D.;Burns J.;Grobler A.C.;Williams S.;Chua J.;Liang C.;Lamont P.J.;Grootendorst A.C.;Massey L.;Sue C.
Monash Health Department(s): Physiotherapy
Allied Health
Institution: (Milne, Corben, Roberts, Delatycki) Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Parkville, VIC, Australia (Milne, Roberts) Physiotherapy Department, Monash Health, Cheltenham, VIC, Australia (Milne, Corben) School of Primary and Allied Health Care, Monash University, Frankston, VIC, Australia (Milne, Corben, Grobler, Delatycki) Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia (Szmulewicz) Balance Disorders and Ataxia Service, Royal Victorian Eye and Ear Hospital, East Melbourne, VIC, Australia (Szmulewicz) Cerebellar Ataxia Clinic, Alfred Health, Caulfield, VIC, Australia (Szmulewicz) Monash Medical Centre, Monash Health, Clayton, VIC, Australia (Szmulewicz) The Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia (Burns) University of Sydney School of Health Sciences, Faculty of Medicine and Health, Children's Hospital at Westmead, Sydney, NSW, Australia (Grobler) Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Parkville, VIC, Australia (Williams) Physiotherapy Department, Royal Perth Hospital, Perth, WA, Australia (Williams) Physiotherapy Department, Sir Charles Gairdner Hospital, Nedlands, WA, Australia (Chua) Physiotherapy Department, Ryde Hospital, Eastwood, NSW, Australia (Liang, Sue) Department of Neurology, Royal North Shore Hospital, St Leonards, NSW, Australia (Liang, Sue) Kolling Institute of Medical Research, University of Sydney, St Leonards, NSW, Australia (Lamont) Neurogenetic Unit, Royal Perth Hospital, Perth, WA, Australia (Grootendorst, Massey, Lagrappe, Willis) Mjd Foundation, Darwin, NT, Australia (Dalziel) Melbourne School of Population and Global Health, University of Melbourne, Parkville, VIC, Australia (Freijah, Gerken) Rehabilitation Services, Royal Darwin and Palmerston Hospitals, Darwin, NT, Australia (Delatycki) Victorian Clinical Genetics Services, Melbourne, VIC, Australia
Issue Date: 26-Apr-2021
Copyright year: 2020
Publisher: BMJ Publishing Group
Place of publication: United Kingdom
Publication information: BMJ Open. 10 (12) (no pagination), 2020. Article Number: e040230. Date of Publication: 17 Dec 2020.
Journal: BMJ Open
Abstract: 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.Copyright ©
DOI: http://monash.idm.oclc.org/login?url=
http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1136/bmjopen-2020-040230
PubMed URL: 33334834 [http://www.ncbi.nlm.nih.gov/pubmed/?term=33334834]
ISSN: 2044-6055 (electronic)
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/26578
Type: Article
Type of Clinical Study or Trial: Randomised controlled trial
Appears in Collections:Articles

Show full item record

Page view(s)

90
checked on Jan 5, 2025

Google ScholarTM

Check


Items in Monash Health Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.