Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/36710
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dc.contributor.authorForbat, Lizen_UK
dc.contributor.authorMacgregor, Aishaen_UK
dc.contributor.authorBrown, Talithaen_UK
dc.contributor.authorMcCormack, Brendanen_UK
dc.contributor.authorSpilsbury, Karenen_UK
dc.contributor.authorRutherford, Alasdairen_UK
dc.contributor.authorHanratty, Barbaraen_UK
dc.contributor.authorHockley, Joen_UK
dc.contributor.authorMcKenzie, Maisieen_UK
dc.contributor.authorSoulsby, Ireneen_UK
dc.contributor.authorOgden, Margareten_UK
dc.date.accessioned2025-03-08T01:19:27Z-
dc.date.available2025-03-08T01:19:27Z-
dc.date.issued2024-09en_UK
dc.identifier.urihttp://hdl.handle.net/1893/36710-
dc.description.abstractPatient and public involvement and engagement (PPIE) is an increasingly important component of research conduct to enhance processes and potential for impact, yet is rarely critically interrogated. This paper draws on Foucauldian analysis to highlight the disciplinary powers and tensions arising in PPIE. The paper draws on a nested evaluation interview study with three PPIE members and eight academics, who had been involved in an implementation science study focused on palliative care. PPIE members were involved in the whole study and are co-authors of this article. Through shared values and commitments to the study, a team culture of equality was developed. Yet while power was dispersed and taken-up by all team members, in so doing a self-governance approach within the team was developed. The pace and focus of discussions was at times more subjugating than co-production. Identities and positions were porous; the simplistic division of ‘academic’ and ‘PPIE’ did not stand up to scrutiny, with an increasing blurring of boundaries as people’s experiences and insights changed over time. Continual, subtle, negotiations of roles, inputs and identities were manifest throughout the project. PPIE in research involves subtle, complex and ongoing disciplinary practices enacted by all members of the team.en_UK
dc.language.isoenen_UK
dc.publisherWileyen_UK
dc.relationForbat L, Macgregor A, Brown T, McCormack B, Spilsbury K, Rutherford A, Hanratty B, Hockley J, McKenzie M, Soulsby I & Ogden M (2024) Negotiating pace, focus and identities: Patient/public involvement/engagement in a palliative care study. <i>Sociology of Health & Illness</i>, 46 (7), pp. 1327-1344. https://doi.org/10.1111/1467-9566.13785en_UK
dc.rights© 2024 The Authors. Sociology of Health & Illness published by John Wiley & Sons Ltd on behalf of Foundation for the Sociology of Health & Illness. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectco-productionen_UK
dc.subjectnegotiationen_UK
dc.subjectpalliative careen_UK
dc.subjectpatient/public involvement and engagementen_UK
dc.subjectpoweren_UK
dc.titleNegotiating pace, focus and identities: Patient/public involvement/engagement in a palliative care studyen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1111/1467-9566.13785en_UK
dc.identifier.pmid38720523en_UK
dc.citation.jtitleSociology of Health and Illnessen_UK
dc.citation.issn1467-9566en_UK
dc.citation.issn0141-9889en_UK
dc.citation.volume46en_UK
dc.citation.issue7en_UK
dc.citation.spage1327en_UK
dc.citation.epage1344en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderNIHR National Institute for Health Researchen_UK
dc.author.emailelizabeth.forbat1@stir.ac.uken_UK
dc.citation.date08/05/2024en_UK
dc.contributor.affiliationFaculty of Social Sciencesen_UK
dc.contributor.affiliationDementia and Ageingen_UK
dc.contributor.affiliationUniversity of Surreyen_UK
dc.contributor.affiliationUniversity of Sydneyen_UK
dc.contributor.affiliationUniversity of Leedsen_UK
dc.contributor.affiliationSociology, Social Policy & Criminologyen_UK
dc.contributor.affiliationNewcastle Universityen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationDementia and Ageingen_UK
dc.contributor.affiliationDementia and Ageingen_UK
dc.identifier.isiWOS:001215920000001en_UK
dc.identifier.scopusid2-s2.0-85192533067en_UK
dc.identifier.wtid2071576en_UK
dc.contributor.orcid0000-0002-7218-5775en_UK
dc.contributor.orcid0000-0001-5812-9323en_UK
dc.contributor.orcid0000-0001-8525-8905en_UK
dc.contributor.orcid0000-0002-6908-0032en_UK
dc.contributor.orcid0000-0003-2530-1195en_UK
dc.contributor.orcid0000-0002-3122-7190en_UK
dc.contributor.orcid0000-0001-5445-0515en_UK
dc.date.accepted2024-03-21en_UK
dcterms.dateAccepted2024-03-21en_UK
dc.date.filedepositdate2024-11-15en_UK
dc.relation.funderprojectImproving end of life care: supporting the workforce and reducing hospitalisations through an implementation study in care homesen_UK
dc.relation.funderrefNIHR128799en_UK
rioxxterms.apcpaiden_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorForbat, Liz|0000-0002-7218-5775en_UK
local.rioxx.authorMacgregor, Aisha|0000-0001-5812-9323en_UK
local.rioxx.authorBrown, Talitha|en_UK
local.rioxx.authorMcCormack, Brendan|0000-0001-8525-8905en_UK
local.rioxx.authorSpilsbury, Karen|0000-0002-6908-0032en_UK
local.rioxx.authorRutherford, Alasdair|0000-0003-2530-1195en_UK
local.rioxx.authorHanratty, Barbara|0000-0002-3122-7190en_UK
local.rioxx.authorHockley, Jo|0000-0001-5445-0515en_UK
local.rioxx.authorMcKenzie, Maisie|en_UK
local.rioxx.authorSoulsby, Irene|en_UK
local.rioxx.authorOgden, Margaret|en_UK
local.rioxx.projectNIHR128799|National Institute for Health Research|http://dx.doi.org/10.13039/501100000272en_UK
local.rioxx.freetoreaddate2024-12-06en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2024-12-06|en_UK
local.rioxx.filenameSociology Health Illness - 2024 - Forbat - Negotiating pace focus and identities Patient public involvement engagement (1).pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1467-9566en_UK
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