Literature DB >> 27660557

Tokenism in patient engagement.

David L Hahn1, Amanda E Hoffmann1, Maret Felzien2, Joseph W LeMaster3, Jinping Xu4, Lyle J Fagnan5.   

Abstract

Background: Patient engagement throughout research is a way to generate more relevant patient-important research questions, methods and results with the ultimate aim of facilitating translation of research into practice. Tokenism is defined as the practice of making perfunctory or symbolic efforts to engage communities or patients. Objective: We wanted to explore how tokenism might influence engaging patients in research to help researchers work towards more genuine engagement.
Methods: The Community Clinician Advisory Group and Patient and Clinician Engagement program held a workshop at the 2015 North American Primary Care Research Group meeting titled 'How Do We Move beyond Tokenism in Patient Engagement?' Patients, clinicians and academic researchers contributed examples of genuine and token engagement characteristics based on personal experience and knowledge. Data were iteratively collated and categorized into domains and items.
Results: Examples of genuine and token engagement were categorized into three domains: Methods/Structure of engagement, Intent and Relationship building. Members with experience in patient-engaged research projects felt that longitudinal engagement was a key element to effectively translating research into local community and practice. Conclusions: The group (i) highly valued genuine intent and relationship building as elements to combat tokenism; (ii) noted that early genuine attempts at engagement may superficially resemble tokenism as researchers build enduring and trusting relationships with patient/community partners and (iii) emphasized the importance of seeking and utilizing patient experiences throughout research. These observations may contribute to more formal methods to help researchers (and reviewers) evaluate where engagement processes sit along the 'genuine-token' continuum.
© The Author 2016. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Culture and disease/cross-cultural issues; doctor–patient relationship; faculty development; health literacy; primary care.

Mesh:

Year:  2017        PMID: 27660557     DOI: 10.1093/fampra/cmw097

Source DB:  PubMed          Journal:  Fam Pract        ISSN: 0263-2136            Impact factor:   2.267


  35 in total

1.  Exploring Ethical Issues Related to Patient Engagement in Healthcare: Patient, Clinician and Researcher's Perspectives.

Authors:  Marjorie Montreuil; Joé T Martineau; Eric Racine
Journal:  J Bioeth Inq       Date:  2019-02-11       Impact factor: 1.352

2.  Integrating the Lived Experience Conditions and Care in the ECHO Model.

Authors:  Tracy Greever-Rice; Lea Brandt; Melissa Warne-Griggs; Kimberly Hoffman
Journal:  Mo Med       Date:  2020 May-Jun

3.  Patients as Agents in Behavioral Health Research and Service Provision: Recommendations to Support the Learning Health System.

Authors:  Hannah K Galvin; Carolyn Petersen; Vignesh Subbian; Anthony Solomonides
Journal:  Appl Clin Inform       Date:  2019-11-06       Impact factor: 2.342

4.  Protocol for a Cluster Randomized Trial Comparing Team-Based to Clinician-Focused Implementation of Advance Care Planning in Primary Care.

Authors:  Annette M Totten; Lyle J Fagnan; David Dorr; LeAnn C Michaels; Shigeko Seiko Izumi; Angela Combe; France Légaré
Journal:  J Palliat Med       Date:  2019-09       Impact factor: 2.947

5.  Defining Patient-Oriented Research for the Average Person (and Potential Research Partner).

Authors:  Dennis J Baumgardner
Journal:  J Patient Cent Res Rev       Date:  2019-01-28

6.  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

7.  Measuring the Impact of Patient-Engaged Research: How a Methods Workshop Identified Critical Outcomes of Research Engagement.

Authors:  Ellis C Dillon; Leah Tuzzio; Sarah Madrid; Heather Olden; Robert T Greenlee
Journal:  J Patient Cent Res Rev       Date:  2017-11-06

8.  Monitoring and Evaluation of Patient Engagement in Health Product Research and Development: Co-Creating a Framework for Community Advisory Boards.

Authors:  Sevgi E Fruytier; Lidewij Eva Vat; Rob Camp; François Houÿez; Hilde De Keyser; Denise Dunne; Davide Marchi; Laura McKeaveney; Richard H Pitt; Carina A C M Pittens; Meagan F Vaughn; Elena Zhuravleva; Tjerk Jan Schuitmaker-Warnaar
Journal:  J Patient Cent Res Rev       Date:  2022-01-17

Review 9.  Conceptualizing and Counting Discretionary Utilization in the Final 100 Days of Life: A Scoping Review.

Authors:  Paul R Duberstein; Michael Chen; Michael Hoerger; Ronald M Epstein; Laura M Perry; Sule Yilmaz; Fahad Saeed; Supriya G Mohile; Sally A Norton
Journal:  J Pain Symptom Manage       Date:  2019-10-19       Impact factor: 3.612

10.  Designing Discrete Choice Experiments Using a Patient-Oriented Approach.

Authors:  Magda Aguiar; Mark Harrison; Sarah Munro; Tiasha Burch; K Julia Kaal; Marie Hudson; Nick Bansback; Tracey-Lea Laba
Journal:  Patient       Date:  2021-07       Impact factor: 3.883

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