Literature DB >> 28289118

The PCORI Engagement Rubric: Promising Practices for Partnering in Research.

Susan Sheridan1, Suzanne Schrandt1,2, Laura Forsythe, Tandrea S Hilliard3, Kathryn A Paez3.   

Abstract

PURPOSE: Engaging patients, caregivers, and other health care stakeholders as partners in planning, conducting, and disseminating research is a promising way to improve clinical decision making and outcomes. Many researchers, patients, and other stakeholders, however, lack clarity about when and how to engage as partners within the clinical research process. To address the need for guidance on creating meaningful stakeholder partnerships in patient-centered clinical comparative effectiveness research, the Patient-Centered Outcomes Research Institute (PCORI) developed the PCORI Engagement Rubric (Rubric).
METHODS: PCORI developed the Rubric drawing from a synthesis of the literature, a qualitative study with patients, a targeted review of engagement plans from PCORI-funded project applications, and a moderated discussion and review with PCORI's Advisory Panel on Patient Engagement.
RESULTS: The Rubric provides a framework for operationalizing engagement to incorporate patients and other stakeholders in all phases of research. It includes: principles of engagement; definitions of stakeholder types; key considerations for planning, conducting, and disseminating engaged research; potential engagement activities; and examples of promising practices from PCORI-funded projects.
CONCLUSIONS: PCORI designed the Rubric to illustrate opportunities for engagement to researchers interested in applying for PCORI funding and to patients and other stakeholders interested in greater involvement in research. By encouraging PCORI applicants, awardees, and others to apply the rubric, PCORI hopes to shift the research paradigm from one of conducting research on patients as subjects to a pursuit carried out in collaboration with patients and other stakeholders to better reflect the values, preferences, and outcomes that matter to the patient community.
© 2017 Annals of Family Medicine, Inc.

Entities:  

Keywords:  patient engagement; patient outcomes; patient-centered

Mesh:

Year:  2017        PMID: 28289118      PMCID: PMC5348236          DOI: 10.1370/afm.2042

Source DB:  PubMed          Journal:  Ann Fam Med        ISSN: 1544-1709            Impact factor:   5.166


  9 in total

1.  Community engagement in research: frameworks for education and peer review.

Authors:  Syed M Ahmed; Ann-Gel S Palermo
Journal:  Am J Public Health       Date:  2010-06-17       Impact factor: 9.308

Review 2.  Participatory action research.

Authors:  Fran Baum; Colin MacDougall; Danielle Smith
Journal:  J Epidemiol Community Health       Date:  2006-10       Impact factor: 3.710

3.  A guided tour of community-based participatory research: an annotated bibliography.

Authors:  John Westfall; Julie Stevenson
Journal:  Ann Fam Med       Date:  2007 Mar-Apr       Impact factor: 5.166

4.  Introduction: lay participation in the history of scientific observation.

Authors:  Jeremy Vetter
Journal:  Sci Context       Date:  2011-06       Impact factor: 0.425

Review 5.  Evaluating patient and stakeholder engagement in research: moving from theory to practice.

Authors:  Laura Esmail; Emily Moore; Alison Rein
Journal:  J Comp Eff Res       Date:  2015-03       Impact factor: 1.744

Review 6.  Mapping the impact of patient and public involvement on health and social care research: a systematic review.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Health Expect       Date:  2012-07-19       Impact factor: 3.377

Review 7.  Use of community-based participatory research in primary care to improve healthcare outcomes and disparities in care.

Authors:  Hazel Tapp; Lauren White; Mark Steuerwald; Michael Dulin
Journal:  J Comp Eff Res       Date:  2013-07       Impact factor: 1.744

8.  Conceptual and practical foundations of patient engagement in research at the patient-centered outcomes research institute.

Authors:  Lori Frank; Laura Forsythe; Lauren Ellis; Suzanne Schrandt; Sue Sheridan; Jason Gerson; Kristen Konopka; Sarah Daugherty
Journal:  Qual Life Res       Date:  2015-01-06       Impact factor: 4.147

Review 9.  Patient engagement in research: a systematic review.

Authors:  Juan Pablo Domecq; Gabriela Prutsky; Tarig Elraiyah; Zhen Wang; Mohammed Nabhan; Nathan Shippee; Juan Pablo Brito; Kasey Boehmer; Rim Hasan; Belal Firwana; Patricia Erwin; David Eton; Jeff Sloan; Victor Montori; Noor Asi; Abd Moain Abu Dabrh; Mohammad Hassan Murad
Journal:  BMC Health Serv Res       Date:  2014-02-26       Impact factor: 2.655

  9 in total
  85 in total

Review 1.  Framework for Advancing the Reporting of Patient Engagement in Rheumatology Research Projects.

Authors:  Clayon B Hamilton; Jenny C Leese; Alison M Hoens; Linda C Li
Journal:  Curr Rheumatol Rep       Date:  2017-07       Impact factor: 4.592

2.  The AASPIRE practice-based guidelines for the inclusion of autistic adults in research as co-researchers and study participants.

Authors:  Christina Nicolaidis; Dora Raymaker; Steven K Kapp; Amelia Baggs; E Ashkenazy; Katherine McDonald; Michael Weiner; Joelle Maslak; Morrigan Hunter; Andrea Joyce
Journal:  Autism       Date:  2019-04-03

3.  Engaging the Patient's Perspective in Clinical Trials Research.

Authors:  Brooke Hefele; Sinéad M Langan; Karen Pollins; Joel M Gelfand
Journal:  J Invest Dermatol       Date:  2019-03-14       Impact factor: 8.551

4.  Integrating multiple community perspectives in intervention development.

Authors:  Yamilï Molina; Karriem S Watson; Liliana G San Miguel; Karen Aguirre; Mariana Hernandez-Flores; Tatiana B Giraldo; Araceli Lucio; Nora Coronado; Phoenix A Matthews
Journal:  Health Educ Res       Date:  2019-08-01

5.  PaTH to partnership in stakeholder-engaged research: A framework for stakeholder engagement in the PaTH to Health Diabetes study.

Authors:  Jennifer M Poger; Hsin-Chieh Yeh; Cindy L Bryce; Jennifer K Carroll; Lan Kong; Erica B Francis; Jennifer L Kraschnewski
Journal:  Healthc (Amst)       Date:  2019-05-14

6.  A proposed framework for patient engagement throughout the broader research enterprise.

Authors:  Camila L Strassle; Steven D Pearson
Journal:  J Comp Eff Res       Date:  2020-04-07       Impact factor: 1.744

7.  Real World Survey of Patient Engagement Status in Clinical Research: The First Input from Japan.

Authors:  Nanae Tanemura; Tsuyoshi Sasaki; Junko Sato; Hisashi Urushihara
Journal:  Patient       Date:  2020-10       Impact factor: 3.883

Review 8.  A New Framework for Patient Engagement in Cancer Clinical Trials Cooperative Group Studies.

Authors:  Patricia A Deverka; Rick Bangs; Karma Kreizenbeck; Deborah M Delaney; Dawn L Hershman; Charles D Blanke; Scott D Ramsey
Journal:  J Natl Cancer Inst       Date:  2018-06-01       Impact factor: 13.506

9.  Patient and Family Advisory Councils (PFACs): Identifying Challenges and Solutions to Support Engagement in Research.

Authors:  James D Harrison; Wendy G Anderson; Maureen Fagan; Edmondo Robinson; Jeffrey Schnipper; Gina Symczak; Catherine Hanson; Martha B Carnie; Jim Banta; Sherry Chen; Jonathan Duong; Celene Wong; Andrew D Auerbach
Journal:  Patient       Date:  2018-08       Impact factor: 3.883

10.  Engagement and partnership with peer mentors in the development of the "Positive and Healthy Living Program": a process paper.

Authors:  Grace Nduku Wambua; Otsetswe Musindo; Judy Machuka; Manasi Kumar
Journal:  AIDS Care       Date:  2019-02-01
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