TY - JOUR
T1 - Development of a web tool to increase research literacy in underserved populations through public library partnerships
AU - Simon, Melissa A.
AU - O'Brian, Catherine A.
AU - Tom, Laura
AU - Eileen Wafford, Q.
AU - Mack, Shenita
AU - Mendez, Samuel R.
AU - Nava, Magdalena
AU - Dahdouh, Rabih
AU - Paul-Brutus, Rachelle
AU - Carpenter, Kathryn H.
AU - Kern, Barbara
AU - Holmes, Kristi L.
N1 - Publisher Copyright:
© 2021 Public Library of Science. All rights reserved.
PY - 2021/2
Y1 - 2021/2
N2 - Objective Inadequate diversity in clinical trials is widely recognized as a significant contributing factor to health disparities experienced by racial/ethnic minorities and other diverse populations in the US. To address this in a scalable way, we sought to develop a web tool that could help enhance underserved minority participation in clinical research. Methods We used our research literacy support flashcard tool as the initial prototype for human-centered design and usability testing of the web tool Health for All in public library settings. After forming partnerships with leadership from Chicago Public Libraries (CPL), local medical libraries, and the Chicago Department of Public Health, we conducted seven iterative design sessions with focus groups of library patrons and library staff from six CPL branches serving underserved communities followed by two rounds of usability testing and website modification. Results Based on the qualitative research findings from Design Sessions 1-7, we enacted the design decision of a website that was a hybrid of fact-filled and vignette (personal stories) paper prototypes divided into 4 modules (trust, diversity, healthy volunteers, pros/cons), each with their own outcome metrics. The website was thus constructed, and navigation issues identified in two rounds of usability testing by library patrons were addressed through further website modification, followed by the launch of a beta version of a hybridized singlescrolling and guided module prototype to allow further development with website analytics. Conclusions We report the development of Health for All, a website designed to enhance racial/ethnic minority participation in clinical trials by imparting research literacy, mitigating distrust engendered by longstanding racism and discrimination, and providing connections to clinical trials recruiting participants.
AB - Objective Inadequate diversity in clinical trials is widely recognized as a significant contributing factor to health disparities experienced by racial/ethnic minorities and other diverse populations in the US. To address this in a scalable way, we sought to develop a web tool that could help enhance underserved minority participation in clinical research. Methods We used our research literacy support flashcard tool as the initial prototype for human-centered design and usability testing of the web tool Health for All in public library settings. After forming partnerships with leadership from Chicago Public Libraries (CPL), local medical libraries, and the Chicago Department of Public Health, we conducted seven iterative design sessions with focus groups of library patrons and library staff from six CPL branches serving underserved communities followed by two rounds of usability testing and website modification. Results Based on the qualitative research findings from Design Sessions 1-7, we enacted the design decision of a website that was a hybrid of fact-filled and vignette (personal stories) paper prototypes divided into 4 modules (trust, diversity, healthy volunteers, pros/cons), each with their own outcome metrics. The website was thus constructed, and navigation issues identified in two rounds of usability testing by library patrons were addressed through further website modification, followed by the launch of a beta version of a hybridized singlescrolling and guided module prototype to allow further development with website analytics. Conclusions We report the development of Health for All, a website designed to enhance racial/ethnic minority participation in clinical trials by imparting research literacy, mitigating distrust engendered by longstanding racism and discrimination, and providing connections to clinical trials recruiting participants.
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U2 - 10.1371/journal.pone.0246098
DO - 10.1371/journal.pone.0246098
M3 - Article
C2 - 33534794
AN - SCOPUS:85100531289
SN - 1932-6203
VL - 16
JO - PloS one
JF - PloS one
IS - 2
M1 - e0246098
ER -