Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27716
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dc.contributor.authorHayward, Kathryn S-
dc.contributor.authorKramer, Sharon F-
dc.contributor.authorDalton, Emily J-
dc.contributor.authorHughes, Gemma R-
dc.contributor.authorBrodtmann, Amy-
dc.contributor.authorChurilov, Leonid-
dc.contributor.authorCloud, Geoffrey-
dc.contributor.authorCorbett, Dale-
dc.contributor.authorJolliffe, Laura-
dc.contributor.authorKaffenberger, Tina-
dc.contributor.authorRethnam, Venesha-
dc.contributor.authorThijs, Vincent N-
dc.contributor.authorWard, Nick-
dc.contributor.authorLannin, Natasha-
dc.contributor.authorBernhardt, Julie-
dc.date2021-10-04-
dc.date.accessioned2021-10-11T04:12:53Z-
dc.date.available2021-10-11T04:12:53Z-
dc.date.issued2021-11-
dc.identifier.citationStroke 2021; 52(11): 3706-3717en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27716-
dc.description.abstractThis systematic review aimed to investigate timing, dose, and efficacy of upper limb intervention during the first 6 months poststroke. Three online databases were searched up to July 2020. Titles/abstracts/full-text were reviewed independently by 2 authors. Randomized and nonrandomized studies that enrolled people within the first 6 months poststroke, aimed to improve upper limb recovery, and completed preintervention and postintervention assessments were included. Risk of bias was assessed using Cochrane reporting tools. Studies were examined by timing (recovery epoch), dose, and intervention type. Two hundred and sixty-one studies were included, representing 228 (n=9704 participants) unique data sets. The number of studies completed increased from one (n=37 participants) between 1980 and 1984 to 91 (n=4417 participants) between 2015 and 2019. Timing of intervention start has not changed (median 38 days, interquartile range [IQR], 22-66) and study sample size remains small (median n=30, IQR 20-48). Most studies were rated high risk of bias (62%). Study participants were enrolled at different recovery epochs: 1 hyperacute (<24 hours), 13 acute (1-7 days), 176 early subacute (8-90 days), 34 late subacute (91-180 days), and 4 were unable to be classified to an epoch. For both the intervention and control groups, the median dose was 45 (IQR, 600-1430) min/session, 1 (IQR, 1-1) session/d, 5 (IQR, 5-5) d/wk for 4 (IQR, 3-5) weeks. The most common interventions tested were electromechanical (n=55 studies), electrical stimulation (n=38 studies), and constraint-induced movement (n=28 studies) therapies. Despite a large and growing body of research, intervention dose and sample size of included studies were often too small to detect clinically important effects. Furthermore, interventions remain focused on subacute stroke recovery with little change in recent decades. A united research agenda that establishes a clear biological understanding of timing, dose, and intervention type is needed to progress stroke recovery research. Prospective Register of Systematic Reviews ID: CRD42018019367/CRD42018111629.en
dc.language.isoeng-
dc.subjectintensityen
dc.subjectstroke rehabilitationen
dc.subjectsystematic reviewen
dc.subjecttimeen
dc.subjectupper extremityen
dc.titleTiming and Dose of Upper Limb Motor Intervention After Stroke: A Systematic Review.en
dc.typeJournal Articleen
dc.identifier.journaltitleStrokeen
dc.identifier.affiliationDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Neuroscience, Central Clinical School, Monash University and Alfred Health, Melbourne, Australiaen
dc.identifier.affiliationMelbourne Medical School, University of Melbourne, Parkville, Australiaen
dc.identifier.affiliationDepartment of Clinical and Movement Neuroscience, UCL Queen Square Institute of Neurology, The National Hospital for Neurology and Neurosurgery, London, United Kingdomen
dc.identifier.affiliationCellular and Molecular Medicine and Canadian Partnership for Stroke Recovery, University of Ottawa, Canadaen
dc.identifier.affiliationCentre for Quality and Patient Safety Research, Institute for Health Transformation, and Alfred Health Partnership, Deakin University, Burwood, Australiaen
dc.identifier.affiliationDepartment of Physiotherapy, University of Melbourne, Heidelberg, Australiaen
dc.identifier.affiliationPhysiotherapyen
dc.identifier.affiliationDepartments of Physiotherapy and Medicine, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Heidelberg, Australiaen
dc.identifier.affiliationNeurologyen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen
dc.identifier.doi10.1161/STROKEAHA.121.034348en
dc.type.contentTexten
dc.identifier.orcid0000-0001-5240-3264en
dc.identifier.orcid0000-0003-2795-6259en
dc.identifier.orcid0000-0003-3920-8530en
dc.identifier.orcid0000-0002-3077-4256en
dc.identifier.orcid0000-0001-9466-2862en
dc.identifier.orcid0000-0002-9807-6606en
dc.identifier.orcid0000-0002-8365-6907en
dc.identifier.orcid0000-0003-0217-4576en
dc.identifier.orcid0000-0002-1369-9442en
dc.identifier.orcid0000-0001-9848-2666en
dc.identifier.orcid0000-0002-0493-8536en
dc.identifier.orcid0000-0002-6614-8417en
dc.identifier.orcid0000-0002-2066-8345en
dc.identifier.orcid0000-0002-2787-8484en
dc.identifier.pubmedid34601901-
local.name.researcherBrodtmann, Amy
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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