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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 |
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container_title | Clinical rehabilitation |
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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 |
format | article |
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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.</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 & 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. 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><subject>Aged</subject><subject>Australia</subject><subject>Citizen participation</subject><subject>Clinical medicine</subject><subject>Clinical research</subject><subject>Communication</subject><subject>Consensus</subject><subject>Data Collection Tools</subject><subject>Delphi Technique</subject><subject>Dysarthria</subject><subject>Dysarthria - etiology</subject><subject>Dysarthria - rehabilitation</subject><subject>Female</subject><subject>Humans</subject><subject>Intelligibility</subject><subject>Male</subject><subject>Measurement</subject><subject>Meetings</subject><subject>Middle Aged</subject><subject>Outcome Assessment, Health Care</subject><subject>Polls & surveys</subject><subject>Speech therapists</subject><subject>Stroke</subject><subject>Stroke - complications</subject><subject>Stroke Rehabilitation</subject><subject>Surveys and Questionnaires</subject><subject>Survivor</subject><subject>United Kingdom</subject><issn>0269-2155</issn><issn>1477-0873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>7QJ</sourceid><recordid>eNp1kUtv1TAQhS1ERS-FH8AGWWLDJsXP2GZToQooUqVuWrG0JvG4NyW5LrZD1X9Prm5bHlU1i1nMN2fm6BDyhrNDzo35wETrBNdaKC4kd8I9IyuujGmYNfI5WW3nzRbYJy9LuWKM2QV9QfallUa11qzI2Xm6gRwKBdqnjDTNtU8T0oKVxpRpuC2Q6zoPQCFWzLTUnH7gR_p9DZWWdZrHQG-QTghlznj0iuxFGAu-vusH5OLL5_Pjk-b07Ou340-nTa-4q41VQSjQImII2hjLlGmZXspg7BlIHjoU2AI3bSsBIzMxOgAHXeC665Q8IEc73eu5mzD0uKkZRn-dhwnyrU8w-H8nm2HtL9MvzznTzkqxKLy_U8jp54yl-mkoPY4jbDDNxQsnrNXKmu2xd_-hV2nOm8Wfl0xZqR3XbqH4jupzKiVjfPiGM7_Nyz_Ka9l5-7eNh437gBbgcAcUuMQ_Z59W_A2CsJ2-</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Mitchell, Claire</creator><creator>Woodward-Nutt, Kate</creator><creator>Dancer, Annette</creator><creator>Taylor, Stephen</creator><creator>Bugler, Joe</creator><creator>Bowen, Audrey</creator><creator>Conroy, Paul</creator><creator>Whelan, Brooke-Mai</creator><creator>Wallace, Sarah J</creator><creator>El Kouaissi, Sabrina</creator><creator>Kirkham, Jamie</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>AFRWT</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><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></search><sort><creationdate>20240601</creationdate><title>Towards a core outcome set for dysarthria after stroke: What should we measure?</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-84d24a52fedd57780476050507efc0a31dbe2e6a17663aef07ff9aa9abd15bb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Australia</topic><topic>Citizen participation</topic><topic>Clinical medicine</topic><topic>Clinical research</topic><topic>Communication</topic><topic>Consensus</topic><topic>Data Collection Tools</topic><topic>Delphi Technique</topic><topic>Dysarthria</topic><topic>Dysarthria - etiology</topic><topic>Dysarthria - rehabilitation</topic><topic>Female</topic><topic>Humans</topic><topic>Intelligibility</topic><topic>Male</topic><topic>Measurement</topic><topic>Meetings</topic><topic>Middle Aged</topic><topic>Outcome Assessment, Health Care</topic><topic>Polls & 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 & Abstracts (ASSIA)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & 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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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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