Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18642
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dc.contributor.authorBernhardt, Julie-
dc.contributor.authorRaffelt, Audrey-
dc.contributor.authorChurilov, Leonid-
dc.contributor.authorLindley, Richard I-
dc.contributor.authorSpeare, Sally-
dc.contributor.authorAncliffe, Jacqueline-
dc.contributor.authorKatijjahbe, Md Ali-
dc.contributor.authorHameed, Shahul-
dc.contributor.authorLennon, Sheila-
dc.contributor.authorMcRae, Anna-
dc.contributor.authorTan, Dawn-
dc.contributor.authorQuiney, Jan-
dc.contributor.authorWilliamson, Hannah C-
dc.contributor.authorCollier, Janice-
dc.contributor.authorDewey, Helen M-
dc.contributor.authorDonnan, Geoffrey A-
dc.contributor.authorLanghorne, Peter-
dc.contributor.authorThrift, Amanda G-
dc.date2015-08-17-
dc.date.accessioned2018-08-30T06:34:04Z-
dc.date.available2018-08-30T06:34:04Z-
dc.date.issued2015-08-17-
dc.identifier.citationBMJ Open 2015; 5(8): e008378-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18642-
dc.description.abstractThe purpose of this paper is to examine potential threats to generalisability of the results of a multicentre randomised controlled trial using data from A Very Early Rehabilitation Trial (AVERT). AVERT is a prospective, parallel group, assessor-blinded randomised clinical trial. This paper presents data assessing the generalisability of AVERT. Acute stroke units at 44 hospitals in 8 countries. The first 20,000 patients screened for AVERT, of whom 1158 were recruited and randomised. We use the Proximal Similarity Model, which considers the person, place, and setting and practice, as a framework for considering generalisability. As well as comparing the recruited patients with the target population, we also performed an exploratory analysis of the demographic, clinical, site and process factors associated with recruitment. The demographics and stroke characteristics of the included patients in the trial were broadly similar to population-based norms, with the exception that AVERT had a greater proportion of men. The most common reason for non-recruitment was late arrival to hospital (ie, >24 h). Overall, being older and female reduced the odds of recruitment to the trial. More women than men were excluded for most of the reasons, including refusal. The odds of exclusion due to early deterioration were particularly high for those with severe stroke (OR=10.4, p<0.001, 95% CI 9.27 to 11.65). A model which explores person, place, and setting and practice factors can provide important information about the external validity of a trial, and could be applied to other clinical trials. Australian New Zealand Clinical Trials Registry (ACTRN12606000185561) and Clinicaltrials.gov (NCT01846247).-
dc.language.isoeng-
dc.subjectGeneralisability-
dc.subjectProximal Similarity Model-
dc.subjectRandomised Control Trial-
dc.subjectRehabilitation-
dc.titleExploring threats to generalisability in a large international rehabilitation trial (AVERT).-
dc.typeJournal Article-
dc.identifier.journaltitleBMJ Open-
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationWestmead Clinical School and The George Institute for Global Health, Westmead Hospital C24, Sydney, New South Wales, Australia-
dc.identifier.affiliationRoyal Perth Hospital, Perth, Western Australia, Australia-
dc.identifier.affiliationPhysiotherapy Unit, Medical Rehabilitation Services Department, UKM Medical Centre, Kuala Lumpur, Malaysia-
dc.identifier.affiliationSingapore General Hospital, Singapore, Singapore-
dc.identifier.affiliationSchool of Health Sciences, Flinders University, Repatriation General Hospital, Daw Park, South Australia, Australia-
dc.identifier.affiliationCommunity and Long Term Conditions Directorate, Auckland District Health Board, Auckland City Hospital, Auckland, New Zealand-
dc.identifier.affiliationDepartment of Physiotherapy, Singapore General Hospital, Singapore, Singapore-
dc.identifier.affiliationRoyal Melbourne Hospital, Parkville, Victoria, Australia-
dc.identifier.affiliationDepartment of Physiotherapy, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationFlorey Institute of Neuroscience and Mental Health, and Faculty of Medicine, Nursing and Health Sciences, Monash University, Box Hill Hospital, Box Hill, Victoria, Australia-
dc.identifier.affiliationFlorey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia-
dc.identifier.affiliationInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK-
dc.identifier.affiliationSchool of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia-
dc.identifier.doi10.1136/bmjopen-2015-008378-
dc.identifier.orcid0000-0002-9807-6606en
dc.identifier.orcid0000-0003-2543-8722en
dc.identifier.pubmedid26283667-
dc.type.austinJournal Article-
dc.type.austinMulticenter Study-
dc.type.austinRandomized Controlled Trial-
dc.type.austinResearch Support, Non-U.S. Gov't-
local.name.researcherChurilov, Leonid
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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