Literature DB >> 25252940

Making patient and public involvement in cancer and palliative research a reality: academic support is vital for success.

Karen Collins1, Jonathan Boote2, David Ardron3, Jacqui Gath3, Tracy Green3, Sam H Ahmedzai3.   

Abstract

OBJECTIVE: Patient and public involvement (PPI) has become an established theme within the UK health research policy and is recognised as an essential force in the drive to improve the quality of services and research. These developments have been particularly rapid in the cancer field.
METHODS: This paper outlines a model of PPI in research (known as the North Trent Cancer Research Network Consumer Research Panel, NTCRN CRP; comprising 38 cancer and palliative care patients/carers) and the key benefits and challenges to effective PPI in cancer research.
RESULTS: The PPI model has become a sustainable, inclusive and effective way of implementing PPI within the cancer context. Challenges include (1) a lack of time and funding available to support the PPI model; (2) tensions between different stakeholder groups when developing and conducting health research; (3) panel members finding it difficult to effectively integrate into research meetings when their role and contribution is not made clear at the outset or when unfamiliar language and jargon are used and not explained; (4) some professionals remain unclear about the role and practical implications of PPI in research. However, notwithstanding its financial and organisational challenges, the way that the NTCRN CRP is supported has provided a solid base for it to flourish.
CONCLUSIONS: PPI provides considerable opportunities for patients and the public to work collaboratively with professionals to influence the cancer research agenda, with the contribution of PPI to the research process being integral to the entire process from the outset, rather than appended to it. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Cancer; Methodological research; Supportive care

Mesh:

Year:  2014        PMID: 25252940     DOI: 10.1136/bmjspcare-2014-000750

Source DB:  PubMed          Journal:  BMJ Support Palliat Care        ISSN: 2045-435X            Impact factor:   3.568


  11 in total

1.  Meeting ethical challenges with authenticity when engaging patients and families in end-of-life and palliative care research: a qualitative study.

Authors:  Matthew DeCamp; Ahmed Alasmar; Stacy Fischer; Jean S Kutner
Journal:  BMC Palliat Care       Date:  2022-05-16       Impact factor: 3.113

Review 2.  Partnering with frail or seriously ill patients in research: a systematic review.

Authors:  Claire Ludwig; Ian D Graham; Wendy Gifford; Josee Lavoie; Dawn Stacey
Journal:  Res Involv Engagem       Date:  2020-09-11

3.  A co-produced method to involve service users in research: the SUCCESS model.

Authors:  Bridie Angela Evans; Alison Porter; Helen Snooks; Vanessa Burholt
Journal:  BMC Med Res Methodol       Date:  2019-02-15       Impact factor: 4.615

Review 4.  Patient and carer involvement in palliative care research: An integrative qualitative evidence synthesis review.

Authors:  Eleni Chambers; Clare Gardiner; Jill Thompson; Jane Seymour
Journal:  Palliat Med       Date:  2019-06-28       Impact factor: 4.762

Review 5.  Ethical considerations for engaging frail and seriously ill patients as partners in research: sub-analysis of a systematic review.

Authors:  Claire Ludwig; Ian D Graham; Josee Lavoie; Wendy Gifford; Dawn Stacey
Journal:  Res Involv Engagem       Date:  2021-01-31

6.  The Role of EUPATI CH in Promoting Patient Involvement in Clinical Research: A Multi-Stakeholder Research Project.

Authors:  Cristiana Sessa; Caecilia Schmid; Angela Tolotti; Annette Magnin; David Haerry; Loris Bonetti; Ingrid Klingmann
Journal:  Front Med (Lausanne)       Date:  2021-12-23

7.  Patient involvement in research priorities (PIRE): a study protocol.

Authors:  Karin Piil; Mary Jarden
Journal:  BMJ Open       Date:  2016-05-24       Impact factor: 2.692

8.  Taking patient and public involvement online: qualitative evaluation of an online forum for palliative care and rehabilitation research.

Authors:  Lisa Jane Brighton; Sophie Pask; Hamid Benalia; Sylvia Bailey; Marion Sumerfield; Jana Witt; Susanne de Wolf-Linder; Simon Noah Etkind; Fliss E M Murtagh; Jonathan Koffman; Catherine J Evans
Journal:  Res Involv Engagem       Date:  2018-05-01

9.  Preparing researchers for patient and public involvement in scientific research: Development of a hands-on learning approach through action research.

Authors:  Maarten de Wit; Anna Beurskens; Barbara Piškur; Esther Stoffers; Albine Moser
Journal:  Health Expect       Date:  2018-02-08       Impact factor: 3.377

10.  Patient and public involvement in palliative care research: What works, and why? A qualitative evaluation.

Authors:  Halle Johnson; Margaret Ogden; Lisa Jane Brighton; Simon Noah Etkind; Adejoke O Oluyase; Emeka Chukwusa; Peihan Yu; Susanne de Wolf-Linder; Pam Smith; Sylvia Bailey; Jonathan Koffman; Catherine J Evans
Journal:  Palliat Med       Date:  2020-09-11       Impact factor: 4.762

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