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dc.contributor.authorGibson, A
dc.contributor.authorWelsman, J
dc.contributor.authorBritten, N
dc.date.accessioned2018-01-10T09:02:46Z
dc.date.issued2017-06-30
dc.description.abstractBACKGROUND: There is a growing literature on evaluating aspects of patient and public involvement (PPI). We have suggested that at the core of successful PPI is the dynamic interaction of different forms of knowledge, notably lay and professional. We have developed a four-dimensional theoretical framework for understanding these interactions. AIM: We explore the practical utility of the theoretical framework as a tool for mapping and evaluating the experience of PPI in health services research. METHODS: We conducted three workshops with different PPI groups in which participants were invited to map their PPI experiences on wall charts representing the four dimensions of our framework. The language used to describe the four dimensions was modified to make it more accessible to lay audiences. Participants were given sticky notes to indicate their own positions on the different dimensions and to write explanatory comments if they wished. Participants' responses were then discussed and analysed as a group. RESULTS: The three groups were distinctive in their mapped responses suggesting different experiences in relation to having a strong or weak voice in their organization, having few or many ways of getting involved, addressing organizational or public concerns and believing that the organization was willing to change or not. DISCUSSION: The framework has practical utility for mapping and evaluating PPI interactions and is sensitive to differences in PPI experiences within and between different organizations. The workshops enabled participants to reflect collaboratively on their experiences with a view to improving PPI experiences and planning for the future.en_GB
dc.description.sponsorshipThis research was funded by the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care South West Peninsula and the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care West.en_GB
dc.identifier.citationVol. 20 (5), pp. 826 - 835en_GB
dc.identifier.doi10.1111/hex.12486
dc.identifier.urihttp://hdl.handle.net/10871/30884
dc.language.isoenen_GB
dc.publisherWileyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/28664563en_GB
dc.rights© 2017 The Authors Health Expectations published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectevaluationen_GB
dc.subjecthealth researchen_GB
dc.subjectknowledge spacesen_GB
dc.subjectmapping experiencesen_GB
dc.subjectpublic involvementen_GB
dc.subjecttheoretical frameworken_GB
dc.titleEvaluating patient and public involvement in health research: from theoretical model to practical workshopen_GB
dc.typeArticleen_GB
dc.date.available2018-01-10T09:02:46Z
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the final version of the article. Available from Wiley via the DOI in this record.en_GB
dc.identifier.journalHealth Expectationsen_GB


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