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

Author:

Johnson Halle1ORCID,Ogden Margaret2,Brighton Lisa Jane1ORCID,Etkind Simon Noah1,Oluyase Adejoke O1ORCID,Chukwusa Emeka1,Yu Peihan1,de Wolf-Linder Susanne3,Smith Pam2,Bailey Sylvia2,Koffman Jonathan1ORCID,Evans Catherine J14

Affiliation:

1. Cicely Saunders Institute of Palliative Care, Policy & Rehabilitation, Florence Nightingale Faculty of Nursing, Midwifery & Palliative Care, King’s College London, London, UK

2. Patient and Public Contributor, Cicely Saunders Institute, King’s College London, London, UK

3. Institute of Nursing, School of Health Professions, Zurich University of Applied Sciences, Winterthur, Switzerland

4. Sussex Community NHS Foundation Trust, Brighton General Hospital, Brighton, UK

Abstract

Background: Public involvement is increasingly considered a prerequisite for high-quality research. However, involvement in palliative care is impeded by limited evidence on the best approaches for populations affected by life-limiting illness. Aim: To evaluate a strategy for public involvement in palliative care and rehabilitation research, to identify successful approaches and areas for improvement. Design: Co-produced qualitative evaluation using focus groups and interviews. Thematic analysis undertaken by research team comprising public contributors and researchers. Setting/participants: Researchers and public members from a palliative care and rehabilitation research institute, UK. Results: Seven public members and 19 researchers participated. Building and maintaining relationships, taking a flexible approach and finding the ‘right’ people were important for successful public involvement. Relationship building created a safe environment for discussing sensitive topics, although public members felt greater consideration of emotional support was needed. Flexibility supported involvement alongside unpredictable circumstances of chronic and life-limiting illness, and was facilitated by responsive communication, and opportunities for in-person and virtual involvement at a project- and institution-level. However, more opportunities for two-way feedback throughout projects was suggested. Finding the ‘right’ people was crucial given the diverse population served by palliative care, and participants suggested more care needed to be taken to identify public members with experience relevant to specific projects. Conclusion: Within palliative care research, it is important for involvement to focus on building and maintaining relationships, working flexibly, and identifying those with relevant experience. Taking a strategic approach and developing adequate infrastructure and networks can facilitate public involvement within this field.

Funder

NIHR Applied Research Collaboration (ARC) South London at King's College Hospital Foundation Trust

national institute for health research

HEE/NIHR Senior Clinical Lectureship

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

Reference31 articles.

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