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Towards a core outcome set for dysarthria after stroke: What should we measure?

Objective To identify and agree on what outcome domains should be measured in research and clinical practice when working with stroke survivors who have dysarthria. Design Delphi process, two rounds of an online survey followed by two online consensus meetings. Setting UK and Australia. Participants...

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Published in:Clinical rehabilitation 2024-06, Vol.38 (6), p.802-810
Main Authors: Mitchell, Claire, Woodward-Nutt, Kate, Dancer, Annette, Taylor, Stephen, Bugler, Joe, Bowen, Audrey, Conroy, Paul, Whelan, Brooke-Mai, Wallace, Sarah J, El Kouaissi, Sabrina, Kirkham, Jamie
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container_end_page 810
container_issue 6
container_start_page 802
container_title Clinical rehabilitation
container_volume 38
creator Mitchell, Claire
Woodward-Nutt, Kate
Dancer, Annette
Taylor, Stephen
Bugler, Joe
Bowen, Audrey
Conroy, Paul
Whelan, Brooke-Mai
Wallace, Sarah J
El Kouaissi, Sabrina
Kirkham, Jamie
description Objective To identify and agree on what outcome domains should be measured in research and clinical practice when working with stroke survivors who have dysarthria. Design Delphi process, two rounds of an online survey followed by two online consensus meetings. Setting UK and Australia. Participants Stroke survivors with experience of dysarthria, speech and language therapists/pathologists working in stroke and communication researchers. Methods Initial list of outcome domains generated from existing literature and with our patient and public involvement group to develop the survey. Participants completed two rounds of this survey to rate importance. Outcomes were identified as ‘in’, ‘unclear’ or ‘out’ from the second survey. All participants were invited to two consensus meetings to discuss these results followed by voting to identify critically important outcome domains for a future Core Outcome Set. All outcomes were voted on in the consensus meetings and included if 70% of meeting participants voted ‘yes’ for critically important. Results In total, 148 surveys were fully completed, and 28 participants attended the consensus meetings. A core outcome set for dysarthria after stroke should include four outcome domains: (a) intelligibility of speech, (b) ability to participate in conversations, (c) living well with dysarthria, (d) skills and knowledge of communication partners (where relevant). Conclusions We describe the consensus of ‘what’ speech outcomes after stroke are valued by all stakeholders including those with lived experience. We share these findings to encourage the measurement of these domains in clinical practice and research and for future research to identify ‘how’ best to measure these outcomes.
doi_str_mv 10.1177/02692155241231929
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Design Delphi process, two rounds of an online survey followed by two online consensus meetings. Setting UK and Australia. Participants Stroke survivors with experience of dysarthria, speech and language therapists/pathologists working in stroke and communication researchers. Methods Initial list of outcome domains generated from existing literature and with our patient and public involvement group to develop the survey. Participants completed two rounds of this survey to rate importance. Outcomes were identified as ‘in’, ‘unclear’ or ‘out’ from the second survey. All participants were invited to two consensus meetings to discuss these results followed by voting to identify critically important outcome domains for a future Core Outcome Set. All outcomes were voted on in the consensus meetings and included if 70% of meeting participants voted ‘yes’ for critically important. Results In total, 148 surveys were fully completed, and 28 participants attended the consensus meetings. A core outcome set for dysarthria after stroke should include four outcome domains: (a) intelligibility of speech, (b) ability to participate in conversations, (c) living well with dysarthria, (d) skills and knowledge of communication partners (where relevant). Conclusions We describe the consensus of ‘what’ speech outcomes after stroke are valued by all stakeholders including those with lived experience. We share these findings to encourage the measurement of these domains in clinical practice and research and for future research to identify ‘how’ best to measure these outcomes.</description><identifier>ISSN: 0269-2155</identifier><identifier>EISSN: 1477-0873</identifier><identifier>DOI: 10.1177/02692155241231929</identifier><identifier>PMID: 38374687</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Aged ; Australia ; Citizen participation ; Clinical medicine ; Clinical research ; Communication ; Consensus ; Data Collection Tools ; Delphi Technique ; Dysarthria ; Dysarthria - etiology ; Dysarthria - rehabilitation ; Female ; Humans ; Intelligibility ; Male ; Measurement ; Meetings ; Middle Aged ; Outcome Assessment, Health Care ; Polls &amp; surveys ; Speech therapists ; Stroke ; Stroke - complications ; Stroke Rehabilitation ; Surveys and Questionnaires ; Survivor ; United Kingdom</subject><ispartof>Clinical rehabilitation, 2024-06, Vol.38 (6), p.802-810</ispartof><rights>The Author(s) 2024</rights><rights>The Author(s) 2024 2024 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c419t-84d24a52fedd57780476050507efc0a31dbe2e6a17663aef07ff9aa9abd15bb43</cites><orcidid>0000-0003-4075-1215 ; 0000-0002-7909-3160 ; 0000-0002-2445-8468 ; 0000-0002-0600-9343</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925,30999,79364</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38374687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitchell, Claire</creatorcontrib><creatorcontrib>Woodward-Nutt, Kate</creatorcontrib><creatorcontrib>Dancer, Annette</creatorcontrib><creatorcontrib>Taylor, Stephen</creatorcontrib><creatorcontrib>Bugler, Joe</creatorcontrib><creatorcontrib>Bowen, Audrey</creatorcontrib><creatorcontrib>Conroy, Paul</creatorcontrib><creatorcontrib>Whelan, Brooke-Mai</creatorcontrib><creatorcontrib>Wallace, Sarah J</creatorcontrib><creatorcontrib>El Kouaissi, Sabrina</creatorcontrib><creatorcontrib>Kirkham, Jamie</creatorcontrib><title>Towards a core outcome set for dysarthria after stroke: What should we measure?</title><title>Clinical rehabilitation</title><addtitle>Clin Rehabil</addtitle><description>Objective To identify and agree on what outcome domains should be measured in research and clinical practice when working with stroke survivors who have dysarthria. Design Delphi process, two rounds of an online survey followed by two online consensus meetings. Setting UK and Australia. Participants Stroke survivors with experience of dysarthria, speech and language therapists/pathologists working in stroke and communication researchers. Methods Initial list of outcome domains generated from existing literature and with our patient and public involvement group to develop the survey. Participants completed two rounds of this survey to rate importance. Outcomes were identified as ‘in’, ‘unclear’ or ‘out’ from the second survey. All participants were invited to two consensus meetings to discuss these results followed by voting to identify critically important outcome domains for a future Core Outcome Set. All outcomes were voted on in the consensus meetings and included if 70% of meeting participants voted ‘yes’ for critically important. Results In total, 148 surveys were fully completed, and 28 participants attended the consensus meetings. A core outcome set for dysarthria after stroke should include four outcome domains: (a) intelligibility of speech, (b) ability to participate in conversations, (c) living well with dysarthria, (d) skills and knowledge of communication partners (where relevant). Conclusions We describe the consensus of ‘what’ speech outcomes after stroke are valued by all stakeholders including those with lived experience. 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surveys</topic><topic>Speech therapists</topic><topic>Stroke</topic><topic>Stroke - complications</topic><topic>Stroke Rehabilitation</topic><topic>Surveys and Questionnaires</topic><topic>Survivor</topic><topic>United Kingdom</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitchell, Claire</creatorcontrib><creatorcontrib>Woodward-Nutt, Kate</creatorcontrib><creatorcontrib>Dancer, Annette</creatorcontrib><creatorcontrib>Taylor, Stephen</creatorcontrib><creatorcontrib>Bugler, Joe</creatorcontrib><creatorcontrib>Bowen, Audrey</creatorcontrib><creatorcontrib>Conroy, Paul</creatorcontrib><creatorcontrib>Whelan, Brooke-Mai</creatorcontrib><creatorcontrib>Wallace, Sarah J</creatorcontrib><creatorcontrib>El Kouaissi, Sabrina</creatorcontrib><creatorcontrib>Kirkham, Jamie</creatorcontrib><collection>SAGE Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical rehabilitation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitchell, Claire</au><au>Woodward-Nutt, Kate</au><au>Dancer, Annette</au><au>Taylor, Stephen</au><au>Bugler, Joe</au><au>Bowen, Audrey</au><au>Conroy, Paul</au><au>Whelan, Brooke-Mai</au><au>Wallace, Sarah J</au><au>El Kouaissi, Sabrina</au><au>Kirkham, Jamie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Towards a core outcome set for dysarthria after stroke: What should we measure?</atitle><jtitle>Clinical rehabilitation</jtitle><addtitle>Clin Rehabil</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>38</volume><issue>6</issue><spage>802</spage><epage>810</epage><pages>802-810</pages><issn>0269-2155</issn><eissn>1477-0873</eissn><abstract>Objective To identify and agree on what outcome domains should be measured in research and clinical practice when working with stroke survivors who have dysarthria. Design Delphi process, two rounds of an online survey followed by two online consensus meetings. Setting UK and Australia. Participants Stroke survivors with experience of dysarthria, speech and language therapists/pathologists working in stroke and communication researchers. Methods Initial list of outcome domains generated from existing literature and with our patient and public involvement group to develop the survey. Participants completed two rounds of this survey to rate importance. Outcomes were identified as ‘in’, ‘unclear’ or ‘out’ from the second survey. All participants were invited to two consensus meetings to discuss these results followed by voting to identify critically important outcome domains for a future Core Outcome Set. All outcomes were voted on in the consensus meetings and included if 70% of meeting participants voted ‘yes’ for critically important. Results In total, 148 surveys were fully completed, and 28 participants attended the consensus meetings. A core outcome set for dysarthria after stroke should include four outcome domains: (a) intelligibility of speech, (b) ability to participate in conversations, (c) living well with dysarthria, (d) skills and knowledge of communication partners (where relevant). Conclusions We describe the consensus of ‘what’ speech outcomes after stroke are valued by all stakeholders including those with lived experience. We share these findings to encourage the measurement of these domains in clinical practice and research and for future research to identify ‘how’ best to measure these outcomes.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>38374687</pmid><doi>10.1177/02692155241231929</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4075-1215</orcidid><orcidid>https://orcid.org/0000-0002-7909-3160</orcidid><orcidid>https://orcid.org/0000-0002-2445-8468</orcidid><orcidid>https://orcid.org/0000-0002-0600-9343</orcidid><oa>free_for_read</oa></addata></record>
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ispartof Clinical rehabilitation, 2024-06, Vol.38 (6), p.802-810
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source Applied Social Sciences Index & Abstracts (ASSIA); SAGE
subjects Aged
Australia
Citizen participation
Clinical medicine
Clinical research
Communication
Consensus
Data Collection Tools
Delphi Technique
Dysarthria
Dysarthria - etiology
Dysarthria - rehabilitation
Female
Humans
Intelligibility
Male
Measurement
Meetings
Middle Aged
Outcome Assessment, Health Care
Polls & surveys
Speech therapists
Stroke
Stroke - complications
Stroke Rehabilitation
Surveys and Questionnaires
Survivor
United Kingdom
title Towards a core outcome set for dysarthria after stroke: What should we measure?
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