Qualitative Exploration of Speech Pathologists' Experiences and Priorities for Aphasia Service Design: Initial Stage of an Experience‐Based Co‐Design Project to Improve Aphasia Services

ABSTRACT Introduction and Aims Stroke survivors with aphasia (impaired language/communication) have poor outcomes and gaps in the clinical implementation of best practice contribute to this. Little is known, however, about speech pathologist perspectives on the touchpoints (key moments shaping exper...

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Veröffentlicht in:Health expectations : an international journal of public participation in health care and health policy 2024-06, Vol.27 (3), p.e14105-n/a
Hauptverfasser: Anemaat, Lisa, Palmer, Victoria J., Copland, David A., Binge, Geoffrey, Druery, Kent, Druery, Julia, Mainstone, Kathryn, Aisthorpe, Bruce, Mainstone, Penelope, Wallace, Sarah J.
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container_issue 3
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container_title Health expectations : an international journal of public participation in health care and health policy
container_volume 27
creator Anemaat, Lisa
Palmer, Victoria J.
Copland, David A.
Binge, Geoffrey
Druery, Kent
Druery, Julia
Mainstone, Kathryn
Aisthorpe, Bruce
Mainstone, Penelope
Wallace, Sarah J.
description ABSTRACT Introduction and Aims Stroke survivors with aphasia (impaired language/communication) have poor outcomes and gaps in the clinical implementation of best practice contribute to this. Little is known, however, about speech pathologist perspectives on the touchpoints (key moments shaping experiences) in the clinical care pathway that have the greatest impact on service delivery nor how this varies by geographical location. We explored the experiences of speech pathologists who provide aphasia services to establish priorities for improvement and design. Methods and Analysis This is the initial experience gathering and priority identification stage of an experience‐based co‐design (EBCD) project. Speech pathologists were recruited from 21 geographically diverse Hospital and Health Services in Queensland, Australia. Speech pathologists working in acute, rehabilitation and community services shared positive and negative experiences of delivering aphasia care in interviews and focus groups. Experiential data were analysed using qualitative thematic analysis to determine touchpoints. Priorities for service design were identified using an adapted nominal group technique. Results Speech pathologists (n = 62) participated in 16 focus groups and nine interviews and shared 132 experiences of delivering aphasia care. Providing care in teams with poor awareness of the impacts of aphasia was identified as a key challenge, as poor patient‐provider communication was perceived to increase risk of adverse outcomes for patients. Speech pathologists identified areas for improvement related to their own professional needs (e.g., greater access to clinical supervision); collaborative health care (e.g., better coordination and interdisciplinary care to increase therapy time); and the service context and environment (e.g., psychological services able to support diverse communication needs). Conclusions Speech pathologist delivery of aphasia services could be improved through increased access to clinical supervision, opportunities for peer debriefing and interdisciplinary care. Priorities for service design varied by geographical location and included: education to support care transitions (remote areas), improved referral pathways and service linkage (regional areas) and dedicated aphasia staffing (metropolitan areas). Patient or Public Contribution A consumer advisory committee comprising people with aphasia (n = 3, authors K.M., K.D. and B.A.), their significant others (n
doi_str_mv 10.1111/hex.14105
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Little is known, however, about speech pathologist perspectives on the touchpoints (key moments shaping experiences) in the clinical care pathway that have the greatest impact on service delivery nor how this varies by geographical location. We explored the experiences of speech pathologists who provide aphasia services to establish priorities for improvement and design. Methods and Analysis This is the initial experience gathering and priority identification stage of an experience‐based co‐design (EBCD) project. Speech pathologists were recruited from 21 geographically diverse Hospital and Health Services in Queensland, Australia. Speech pathologists working in acute, rehabilitation and community services shared positive and negative experiences of delivering aphasia care in interviews and focus groups. Experiential data were analysed using qualitative thematic analysis to determine touchpoints. Priorities for service design were identified using an adapted nominal group technique. Results Speech pathologists (n = 62) participated in 16 focus groups and nine interviews and shared 132 experiences of delivering aphasia care. Providing care in teams with poor awareness of the impacts of aphasia was identified as a key challenge, as poor patient‐provider communication was perceived to increase risk of adverse outcomes for patients. Speech pathologists identified areas for improvement related to their own professional needs (e.g., greater access to clinical supervision); collaborative health care (e.g., better coordination and interdisciplinary care to increase therapy time); and the service context and environment (e.g., psychological services able to support diverse communication needs). Conclusions Speech pathologist delivery of aphasia services could be improved through increased access to clinical supervision, opportunities for peer debriefing and interdisciplinary care. Priorities for service design varied by geographical location and included: education to support care transitions (remote areas), improved referral pathways and service linkage (regional areas) and dedicated aphasia staffing (metropolitan areas). Patient or Public Contribution A consumer advisory committee comprising people with aphasia (n = 3, authors K.M., K.D. and B.A.), their significant others (n = 2, authors J.D. and P.M.), and a Cultural Capability Officer (author G.B.) guided this research. The team: (1) reviewed participant information; (2) co‐designed surveys and workshop resources; (3) copresented research outcomes and contributed to publications. Research questions and study design (e.g., analysis methods and assessment measures) were developed by the research team (authors L.A., V.J.P., D.A.C. and S.J.W.).</description><identifier>ISSN: 1369-6513</identifier><identifier>ISSN: 1369-7625</identifier><identifier>EISSN: 1369-7625</identifier><identifier>DOI: 10.1111/hex.14105</identifier><identifier>PMID: 38879788</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Access ; Advisory committees ; Aphasia ; Aphasia - therapy ; Best practice ; Clinical outcomes ; Co-design ; Communication ; Community services ; Coordination ; coproduction ; Data collection ; Debriefing ; Design analysis ; Experience ; Female ; Focus Groups ; Geographical distribution ; Geographical locations ; Health care management ; Health services ; Humans ; Interdisciplinary aspects ; Interviews ; Interviews as Topic ; Male ; Medical referrals ; Metropolitan areas ; Negative experiences ; Nominal group technique ; Original ; Pandemics ; Patient communication ; Patients ; patient‐centred care ; Priorities ; Psychological services ; qualitative ; Qualitative analysis ; Qualitative Research ; Queensland ; Rehabilitation ; Research design ; Risk perception ; Service design ; Speech ; Speech-Language Pathology ; Stroke ; Stroke - complications ; Stroke - therapy ; Supervision ; Teams</subject><ispartof>Health expectations : an international journal of public participation in health care and health policy, 2024-06, Vol.27 (3), p.e14105-n/a</ispartof><rights>2024 The Author(s). published by John Wiley &amp; Sons Ltd.</rights><rights>2024 The Author(s). Health Expectations published by John Wiley &amp; Sons Ltd.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Little is known, however, about speech pathologist perspectives on the touchpoints (key moments shaping experiences) in the clinical care pathway that have the greatest impact on service delivery nor how this varies by geographical location. We explored the experiences of speech pathologists who provide aphasia services to establish priorities for improvement and design. Methods and Analysis This is the initial experience gathering and priority identification stage of an experience‐based co‐design (EBCD) project. Speech pathologists were recruited from 21 geographically diverse Hospital and Health Services in Queensland, Australia. Speech pathologists working in acute, rehabilitation and community services shared positive and negative experiences of delivering aphasia care in interviews and focus groups. Experiential data were analysed using qualitative thematic analysis to determine touchpoints. Priorities for service design were identified using an adapted nominal group technique. Results Speech pathologists (n = 62) participated in 16 focus groups and nine interviews and shared 132 experiences of delivering aphasia care. Providing care in teams with poor awareness of the impacts of aphasia was identified as a key challenge, as poor patient‐provider communication was perceived to increase risk of adverse outcomes for patients. Speech pathologists identified areas for improvement related to their own professional needs (e.g., greater access to clinical supervision); collaborative health care (e.g., better coordination and interdisciplinary care to increase therapy time); and the service context and environment (e.g., psychological services able to support diverse communication needs). Conclusions Speech pathologist delivery of aphasia services could be improved through increased access to clinical supervision, opportunities for peer debriefing and interdisciplinary care. Priorities for service design varied by geographical location and included: education to support care transitions (remote areas), improved referral pathways and service linkage (regional areas) and dedicated aphasia staffing (metropolitan areas). Patient or Public Contribution A consumer advisory committee comprising people with aphasia (n = 3, authors K.M., K.D. and B.A.), their significant others (n = 2, authors J.D. and P.M.), and a Cultural Capability Officer (author G.B.) guided this research. The team: (1) reviewed participant information; (2) co‐designed surveys and workshop resources; (3) copresented research outcomes and contributed to publications. 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Little is known, however, about speech pathologist perspectives on the touchpoints (key moments shaping experiences) in the clinical care pathway that have the greatest impact on service delivery nor how this varies by geographical location. We explored the experiences of speech pathologists who provide aphasia services to establish priorities for improvement and design. Methods and Analysis This is the initial experience gathering and priority identification stage of an experience‐based co‐design (EBCD) project. Speech pathologists were recruited from 21 geographically diverse Hospital and Health Services in Queensland, Australia. Speech pathologists working in acute, rehabilitation and community services shared positive and negative experiences of delivering aphasia care in interviews and focus groups. Experiential data were analysed using qualitative thematic analysis to determine touchpoints. Priorities for service design were identified using an adapted nominal group technique. Results Speech pathologists (n = 62) participated in 16 focus groups and nine interviews and shared 132 experiences of delivering aphasia care. Providing care in teams with poor awareness of the impacts of aphasia was identified as a key challenge, as poor patient‐provider communication was perceived to increase risk of adverse outcomes for patients. Speech pathologists identified areas for improvement related to their own professional needs (e.g., greater access to clinical supervision); collaborative health care (e.g., better coordination and interdisciplinary care to increase therapy time); and the service context and environment (e.g., psychological services able to support diverse communication needs). Conclusions Speech pathologist delivery of aphasia services could be improved through increased access to clinical supervision, opportunities for peer debriefing and interdisciplinary care. Priorities for service design varied by geographical location and included: education to support care transitions (remote areas), improved referral pathways and service linkage (regional areas) and dedicated aphasia staffing (metropolitan areas). Patient or Public Contribution A consumer advisory committee comprising people with aphasia (n = 3, authors K.M., K.D. and B.A.), their significant others (n = 2, authors J.D. and P.M.), and a Cultural Capability Officer (author G.B.) guided this research. The team: (1) reviewed participant information; (2) co‐designed surveys and workshop resources; (3) copresented research outcomes and contributed to publications. Research questions and study design (e.g., analysis methods and assessment measures) were developed by the research team (authors L.A., V.J.P., D.A.C. and S.J.W.).</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38879788</pmid><doi>10.1111/hex.14105</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-0600-9343</orcidid><orcidid>https://orcid.org/0009-0006-9081-0649</orcidid><orcidid>https://orcid.org/0009-0005-3652-5698</orcidid><orcidid>https://orcid.org/0009-0008-6532-5443</orcidid><orcidid>https://orcid.org/0009-0002-6594-5307</orcidid><orcidid>https://orcid.org/0000-0002-2257-4270</orcidid><orcidid>https://orcid.org/0009-0004-2642-735X</orcidid><orcidid>https://orcid.org/0000-0001-7410-4652</orcidid><orcidid>https://orcid.org/0000-0001-7212-932X</orcidid><orcidid>https://orcid.org/0009-0005-0714-1505</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1369-6513
ispartof Health expectations : an international journal of public participation in health care and health policy, 2024-06, Vol.27 (3), p.e14105-n/a
issn 1369-6513
1369-7625
1369-7625
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source Applied Social Sciences Index & Abstracts (ASSIA); MEDLINE; Wiley-Blackwell Open Access Titles; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Sociological Abstracts
subjects Access
Advisory committees
Aphasia
Aphasia - therapy
Best practice
Clinical outcomes
Co-design
Communication
Community services
Coordination
coproduction
Data collection
Debriefing
Design analysis
Experience
Female
Focus Groups
Geographical distribution
Geographical locations
Health care management
Health services
Humans
Interdisciplinary aspects
Interviews
Interviews as Topic
Male
Medical referrals
Metropolitan areas
Negative experiences
Nominal group technique
Original
Pandemics
Patient communication
Patients
patient‐centred care
Priorities
Psychological services
qualitative
Qualitative analysis
Qualitative Research
Queensland
Rehabilitation
Research design
Risk perception
Service design
Speech
Speech-Language Pathology
Stroke
Stroke - complications
Stroke - therapy
Supervision
Teams
title Qualitative Exploration of Speech Pathologists' Experiences and Priorities for Aphasia Service Design: Initial Stage of an Experience‐Based Co‐Design Project to Improve Aphasia Services
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