Literature DB >> 31713031

Engaging Patients and Other Non-Researchers in Health Research: Defining Research Engagement.

Lori Frank1, Sally C Morton2, Jeanne-Marie Guise3, Janet Jull4, Thomas W Concannon5, Peter Tugwell6.   

Abstract

With the increase in patient and consumer activism through the late twentieth century and into this century, patient roles in research evolved into a new model of research engagement, with patients serving as active advisors and co-leading or leading clinical research. By requiring active engagement of patients and other stakeholders, several government research funders have advanced this model, particularly in Canada, the United States (US), United Kingdom (UK), and Australia. A consortium of individuals from these countries formed a Multi-Stakeholder Engagement (MuSE) consortium to examine critical issues in engaged research, establish consensus on definitions, and provide guidance for the field, beginning with an overview of how to involve stakeholders in health research (Concannon et al. J Gen Intern Med. 2019;34(3):458-463) and continuing here with an examination of definitions of research engagement. The political and advocacy roots of engaged research are reflected in definitions. Engagement is conceptualized with reference to research project goals, from informing specific clinical decisions to informing health-system level decisions. Political and cultural differences across countries are evident. Some of these government funders focus on empirical rather than ethical rationales. In countries with centralized health technology assessment, the link between societal values and engaged research is explicit. Ethical rationales for engagement are explicit in most of the published literature on research engagement. Harmonization of definitions is recommended so that research engagement elements, methods, and outcomes and impacts can be clearly examined and understood, and so that the field of research engagement can proceed from a clear conceptual foundation. Specific recommendations for terminology definitions are provided. Placing engaged research on a continuum from specific clinical decisions to more global public and social justice concerns clarifies the type of engaged research, supports appropriate comparisons, and improves the rigor of engaged research methods. The results help identify knowledge gaps in this growing field.

Entities:  

Keywords:  international health; patient engagement; patient-centered outcomes research; stakeholder engagement

Mesh:

Year:  2019        PMID: 31713031      PMCID: PMC7048327          DOI: 10.1007/s11606-019-05436-2

Source DB:  PubMed          Journal:  J Gen Intern Med        ISSN: 0884-8734            Impact factor:   5.128


  16 in total

1.  The James Lind Alliance: patients and clinicians should jointly identify their priorities for clinical trials.

Authors:  Nick Partridge; John Scadding
Journal:  Lancet       Date:  2004 Nov 27-Dec 3       Impact factor: 79.321

2.  Public health activism: lessons from history?

Authors:  Virginia Berridge
Journal:  BMJ       Date:  2007-12-22

3.  Practical Guidance for Involving Stakeholders in Health Research.

Authors:  Thomas W Concannon; Sean Grant; Vivian Welch; Jennifer Petkovic; Joseph Selby; Sally Crowe; Anneliese Synnot; Regina Greer-Smith; Evan Mayo-Wilson; Ellen Tambor; Peter Tugwell
Journal:  J Gen Intern Med       Date:  2018-12-18       Impact factor: 5.128

4.  Public involvement in research: making sense of the diversity.

Authors:  Sandy Oliver; Kristin Liabo; Ruth Stewart; Rebecca Rees
Journal:  J Health Serv Res Policy       Date:  2014-09-15

5.  PPI: understanding the difference between patient and public involvement.

Authors:  Jonathan Warsh
Journal:  Am J Bioeth       Date:  2014       Impact factor: 11.229

6.  Collective enquiry and reflective action in research: towards a clarification of the terminology.

Authors:  Felicity Goodyear-Smith
Journal:  Fam Pract       Date:  2017-06-01       Impact factor: 2.267

7.  Revolution or evolution: the challenges of conceptualizing patient and public involvement in a consumerist world.

Authors:  Jonathan Q Tritter
Journal:  Health Expect       Date:  2009-09       Impact factor: 3.377

8.  The science of stakeholder engagement in research: classification, implementation, and evaluation.

Authors:  Melody S Goodman; Vetta L Sanders Thompson
Journal:  Transl Behav Med       Date:  2017-09       Impact factor: 3.046

9.  Practicing partnered research.

Authors:  Joe V Selby; Jean R Slutsky
Journal:  J Gen Intern Med       Date:  2014-12       Impact factor: 5.128

10.  Patient and citizen participation in health: the need for improved ethical support.

Authors:  Laura Williamson
Journal:  Am J Bioeth       Date:  2014       Impact factor: 11.229

View more
  5 in total

1.  Strategies of community engagement in research: definitions and classifications.

Authors:  Vetta L Sanders Thompson; Nicole Ackermann; Kyla L Bauer; Deborah J Bowen; Melody S Goodman
Journal:  Transl Behav Med       Date:  2021-03-16       Impact factor: 3.046

2.  Engaging Stakeholders in the Design and Conduct of Embedded Pragmatic Clinical Trials for Alzheimer's Disease and Alzheimer's Disease-Related Dementias.

Authors:  Jill Harrison; Katie Maslow; Ellen Tambor; Louise Phillips; Lori Frank; Laurie Herndon; Gary Epstein-Lubow
Journal:  J Am Geriatr Soc       Date:  2020-07       Impact factor: 5.562

Review 3.  The Precision Interventions for Severe and/or Exacerbation-Prone (PrecISE) Asthma Network: An overview of Network organization, procedures, and interventions.

Authors:  Steve N Georas; Rosalind J Wright; Anastasia Ivanova; Elliot Israel; Lisa M LaVange; Praveen Akuthota; Tara F Carr; Loren C Denlinger; Merritt L Fajt; Rajesh Kumar; Wanda K O'Neal; Wanda Phipatanakul; Stanley J Szefler; Mark A Aronica; Leonard B Bacharier; Allison J Burbank; Mario Castro; Laura Crotty Alexander; Julie Bamdad; Juan Carlos Cardet; Suzy A A Comhair; Ronina A Covar; Emily A DiMango; Kim Erwin; Serpil C Erzurum; John V Fahy; Jonathan M Gaffin; Benjamin Gaston; Lynn B Gerald; Eric A Hoffman; Fernando Holguin; Daniel J Jackson; John James; Nizar N Jarjour; Nicholas J Kenyon; Sumita Khatri; John P Kirwan; Monica Kraft; Jerry A Krishnan; Andrew H Liu; Mark C Liu; M Alison Marquis; Fernando Martinez; Jacob Mey; Wendy C Moore; James N Moy; Victor E Ortega; David B Peden; Emily Pennington; Michael C Peters; Kristie Ross; Maria Sanchez; Lewis J Smith; Ronald L Sorkness; Michael E Wechsler; Sally E Wenzel; Steven R White; Joe Zein; Amir A Zeki; Patricia Noel
Journal:  J Allergy Clin Immunol       Date:  2021-11-29       Impact factor: 14.290

4.  Partnering to Increase Colorectal Cancer Screening: Perspectives of Community Advisory Board Members.

Authors:  Susan M Rawl; Sandra Bailey; Beatrice Cork; Matthew Fields; Thomas Griffin; Laura Haunert; Judy Kline; Connie Krier; Juan Lagunes; Ruth L Lambert; Caeli Malloy; Jack Quick; Rivienne Shedd-Steele; Sylvia Strom; Lisa Carter-Harris
Journal:  West J Nurs Res       Date:  2021-02-15       Impact factor: 1.967

5.  Engaging multi-stakeholder perspectives to identify dementia care research priorities.

Authors:  Neela K Patel; Sara S Masoud; Kylie Meyer; Angelica V Davila; Sheran Rivette; Ashlie A Glassner; Deborah James; Carole L White
Journal:  J Patient Rep Outcomes       Date:  2021-06-22
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.