Literature DB >> 28949867

How are PCORI-funded researchers engaging patients in research and what are the ethical implications?

Lauren E Ellis1, Nancy E Kass2.   

Abstract

BACKGROUND: Despite growing interest in patient engagement in research, there are few empirical investigations of the nature of engagement and its effects. This information is important, not only to inform practical decisions researchers and funders must make, but also to inform discussion of the ethical implications of engaging patients, which has received little attention to date.
METHODS: The aim of this study was to characterize patient engagement in research funded by the Patient-Centered Outcomes Research Institute (PCORI) as a step toward enhancing current understanding of the nature and effects of engagement and prompting an in-depth consideration of the ethical implications of engaging patients in research. Qualitative interviews were conducted with 19 PCORI-funded principal investigators and with 33 patients engaged in 18 of the same 19 projects.
RESULTS: Reasons cited for engaging patients included to enhance relevance and feasibility and to improve dissemination. While engagement occurred at different points during the research, patients were most commonly engaged in reviewing study materials and less commonly engaged at earlier points. Engagement varied by approach, frequency of interaction, and the extent to which patient input changed the research. Impacts of engagement included improving the relevance, feasibility, acceptability, and quality of the research.
CONCLUSION: Our findings on the nature and impacts of engagement have importance not only for practical questions researchers, funders, and patients might raise, but also for several ethical considerations regarding patient engagement related to why patients are engaged, the kinds of patients engaged, when patients are engaged, and how patients are engaged. We discuss our findings in consideration of the main ethical issues they imply, including ethical rationales for engagement, justice-related concerns, and ethical concerns arising from when and how patients are engaged. As efforts to engage patients increase, this discussion provides insights that researchers, funders, and patients may find valuable.

Entities:  

Keywords:  patient engagement; patient-centered outcomes research; qualitative methods; research ethics

Mesh:

Year:  2016        PMID: 28949867     DOI: 10.1080/23294515.2016.1206045

Source DB:  PubMed          Journal:  AJOB Empir Bioeth        ISSN: 2329-4515


  14 in total

1.  Using the diffusion of innovations model to guide participant engagement in the genomics era.

Authors:  Katie L Lewis; Flavia M Facio; Courtney D Berrios
Journal:  J Genet Couns       Date:  2019-01-17       Impact factor: 2.537

2.  The Role of Participants in a Medical Information Commons.

Authors:  Mary A Majumder; Juli M Bollinger; Angela G Villanueva; Patricia A Deverka; Barbara A Koenig
Journal:  J Law Med Ethics       Date:  2019-03       Impact factor: 1.718

3.  Patients as research partners; how to value their perceptions, contribution and labor?

Authors:  Elise Smith; Jean-Chrisophe Bélisle-Pipon; David Resnik
Journal:  Citiz Sci       Date:  2019-03-08

4.  Go Slow to Go Fast: Successful Engagement Strategies for Patient-Centered, Multi-Site Research, Involving Academic and Community-Based Organizations.

Authors:  Laura T Pinsoneault; Emily R Connors; Elizabeth A Jacobs; Jerica Broeckling
Journal:  J Gen Intern Med       Date:  2018-10-23       Impact factor: 5.128

5.  Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons.

Authors:  Amy L McGuire; Mary A Majumder; Angela G Villanueva; Jessica Bardill; Juli M Bollinger; Eric Boerwinkle; Tania Bubela; Patricia A Deverka; Barbara J Evans; Nanibaa' A Garrison; David Glazer; Melissa M Goldstein; Henry T Greely; Scott D Kahn; Bartha M Knoppers; Barbara A Koenig; J Mark Lambright; John E Mattison; Christopher O'Donnell; Arti K Rai; Laura L Rodriguez; Tania Simoncelli; Sharon F Terry; Adrian M Thorogood; Michael S Watson; John T Wilbanks; Robert Cook-Deegan
Journal:  J Law Med Ethics       Date:  2019-03       Impact factor: 1.718

Review 6.  Considerations for the Design and Implementation of COVID-19 Contact Tracing Apps: Scoping Review.

Authors:  Esli Osmanlliu; Edmond Rafie; Sylvain Bédard; Jesseca Paquette; Genevieve Gore; Marie-Pascale Pomey
Journal:  JMIR Mhealth Uhealth       Date:  2021-06-09       Impact factor: 4.773

7.  Engaging patients in health research: identifying research priorities through community town halls.

Authors:  Holly Etchegary; Lisa Bishop; Catherine Street; Kris Aubrey-Bassler; Dale Humphries; Lidewij Eva Vat; Brendan Barrett
Journal:  BMC Health Serv Res       Date:  2017-03-11       Impact factor: 2.655

8.  IRB Oversight of Patient-Centered Outcomes Research: A National Survey of IRB Chairpersons.

Authors:  Joel S Weissman; Eric G Campbell; I Glenn Cohen; Holly Fernandez Lynch; Emily A Largent; Avni Gupta; Ronen Rozenblum; Melissa Abraham; Karen Spikes; Maureen Fagan; Martie Carnie
Journal:  J Empir Res Hum Res Ethics       Date:  2018-06-14       Impact factor: 1.742

9.  Participant Engagement in Translational Genomics Research: Respect for Persons-and Then Some.

Authors:  Janet E Childerhose; Candice R Finnila; Joon-Ho Yu; Barbara A Koenig; Jean McEwen; Stacey L Berg; Benjamin S Wilfond; Paul S Appelbaum; Kyle B Brothers
Journal:  Ethics Hum Res       Date:  2019-09

Review 10.  Partnering with patients in healthcare research: a scoping review of ethical issues, challenges, and recommendations for practice.

Authors:  Joé T Martineau; Asma Minyaoui; Antoine Boivin
Journal:  BMC Med Ethics       Date:  2020-05-11       Impact factor: 2.652

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