Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research

Our philosophical framework for research with low-income Latino patients with diabetes prioritizes hiring research staff who share the culture and language of the population of study. Inclusive research design requires an active role by patient stakeholders with training opportunities in a collabora...

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Main Authors: Hannah Cole McGrew, Lidia Regino, Molly Bleecker, Maria Tellez, Blanca Pedigo, Denisse Guerrero, Virginia Sandoval, Loida Varela, Janet Page-Reeves
Format: Article
Language:English
Published: The University of Alabama 2022-07-01
Series:Journal of Community Engagement and Scholarship
Online Access:https://account.jces.ua.edu/index.php/s-j-jces/article/view/119
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author Hannah Cole McGrew
Lidia Regino
Molly Bleecker
Maria Tellez
Blanca Pedigo
Denisse Guerrero
Virginia Sandoval
Loida Varela
Janet Page-Reeves
author_facet Hannah Cole McGrew
Lidia Regino
Molly Bleecker
Maria Tellez
Blanca Pedigo
Denisse Guerrero
Virginia Sandoval
Loida Varela
Janet Page-Reeves
author_sort Hannah Cole McGrew
collection DOAJ
description Our philosophical framework for research with low-income Latino patients with diabetes prioritizes hiring research staff who share the culture and language of the population of study. Inclusive research design requires an active role by patient stakeholders with training opportunities in a collaborative learning environment to allow patient stakeholder data collectors (PSDCs) to build on existing strengths and expertise. To develop this manuscript, our team reflected on our collective experiences in implementing research-specific trainings for PSDCs. Although our population of study is known to be difficult to recruit and retain, our PSDCs have successfully enrolled participants on schedule, and attrition is low. Although language, institutional requirements, and funding restrictions presented training challenges, we overcame these by using a flexible approach and by incorporating the data collectors’ expertise in refining our protocols. We propose that our success in recruiting and retaining participants is a reflection of our engaged research strategy and framework and demonstrates that engagement promotes better science. However, our experience also demonstrates research institutions need to make policy and infrastructural improvements to reduce barriers and make engaged approaches more feasible.
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spelling doaj.art-a4a879645b8c4a14af71f4379afb25502023-08-29T21:04:57ZengThe University of AlabamaJournal of Community Engagement and Scholarship1944-12072837-80752022-07-0113110.54656/CZLO2473Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in ResearchHannah Cole McGrew0Lidia Regino1Molly Bleecker2Maria Tellez3Blanca Pedigo4Denisse Guerrero5Virginia Sandoval6Loida Varela7Janet Page-Reeves8University of New MexicoUniversity of New MexicoUniversity of New MexicoOne Hope Centro de Vida Health CenterOne Hope Centro de Vida Health CenterOne Hope Centro de Vida Health CenterOne Hope Centro de Vida Health CenterOne Hope Centro de Vida Health CenterUniversity of New MexicoOur philosophical framework for research with low-income Latino patients with diabetes prioritizes hiring research staff who share the culture and language of the population of study. Inclusive research design requires an active role by patient stakeholders with training opportunities in a collaborative learning environment to allow patient stakeholder data collectors (PSDCs) to build on existing strengths and expertise. To develop this manuscript, our team reflected on our collective experiences in implementing research-specific trainings for PSDCs. Although our population of study is known to be difficult to recruit and retain, our PSDCs have successfully enrolled participants on schedule, and attrition is low. Although language, institutional requirements, and funding restrictions presented training challenges, we overcame these by using a flexible approach and by incorporating the data collectors’ expertise in refining our protocols. We propose that our success in recruiting and retaining participants is a reflection of our engaged research strategy and framework and demonstrates that engagement promotes better science. However, our experience also demonstrates research institutions need to make policy and infrastructural improvements to reduce barriers and make engaged approaches more feasible.https://account.jces.ua.edu/index.php/s-j-jces/article/view/119
spellingShingle Hannah Cole McGrew
Lidia Regino
Molly Bleecker
Maria Tellez
Blanca Pedigo
Denisse Guerrero
Virginia Sandoval
Loida Varela
Janet Page-Reeves
Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research
Journal of Community Engagement and Scholarship
title Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research
title_full Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research
title_fullStr Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research
title_full_unstemmed Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research
title_short Training Patient Stakeholders Builds Community Capacity, Enhances Patient Engagement in Research
title_sort training patient stakeholders builds community capacity enhances patient engagement in research
url https://account.jces.ua.edu/index.php/s-j-jces/article/view/119
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