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Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials
The coronavirus disease 2019 (COVID-19) pandemic has disproportionately affected racial/ethnic minorities in the United States, who are underrepresented in clinical trials. We assessed the feasibility of using the University of Pennsylvania Health System electronic health record patient portal to di...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642328/ https://www.ncbi.nlm.nih.gov/pubmed/36380851 http://dx.doi.org/10.1093/jamiaopen/ooac091 |
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author | Yuh, Tiffany Srivastava, Tuhina Fiore, Danielle Schmidt, Harald Frank, Ian Metzger, David Momplaisir, Florence |
author_facet | Yuh, Tiffany Srivastava, Tuhina Fiore, Danielle Schmidt, Harald Frank, Ian Metzger, David Momplaisir, Florence |
author_sort | Yuh, Tiffany |
collection | PubMed |
description | The coronavirus disease 2019 (COVID-19) pandemic has disproportionately affected racial/ethnic minorities in the United States, who are underrepresented in clinical trials. We assessed the feasibility of using the University of Pennsylvania Health System electronic health record patient portal to diversify the pool of participants in COVID-19 vaccine clinical trials. The patient portal was used to send invitations to eligible individuals living in zip codes with high rates of racial/ethnic minorities. The 5614 invited consisted of 96.7% black, 1.3% Hispanic/Latinx, and 1.5% white. The overall response rate was 5.4%, with lower response rates among Black (3.8%) and Hispanic/Latinx (9.6%) as compared to white individuals (91.6%). Among respondents, black individuals had lower rates of interest in participating (26.7%), as compared to white (65.8%) and Hispanic/Latinx (71.4%) individuals. Of 115 respondents who expressed interest, 9 enrolled in the clinical trial, which included 6 black, 3 white, and 1 Hispanic/Latinx. During phone outreach to nonresponders and decliners, common reasons for declining included mistrust of the COVID-19 vaccine, underlying health conditions, and logistical barriers to trial participation. Because of low rates of patient portal account activation and use, compounded with vaccine hesitancy, this method yielded a small number of interested individuals. |
format | Online Article Text |
id | pubmed-9642328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96423282022-11-14 Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials Yuh, Tiffany Srivastava, Tuhina Fiore, Danielle Schmidt, Harald Frank, Ian Metzger, David Momplaisir, Florence JAMIA Open Brief Communications The coronavirus disease 2019 (COVID-19) pandemic has disproportionately affected racial/ethnic minorities in the United States, who are underrepresented in clinical trials. We assessed the feasibility of using the University of Pennsylvania Health System electronic health record patient portal to diversify the pool of participants in COVID-19 vaccine clinical trials. The patient portal was used to send invitations to eligible individuals living in zip codes with high rates of racial/ethnic minorities. The 5614 invited consisted of 96.7% black, 1.3% Hispanic/Latinx, and 1.5% white. The overall response rate was 5.4%, with lower response rates among Black (3.8%) and Hispanic/Latinx (9.6%) as compared to white individuals (91.6%). Among respondents, black individuals had lower rates of interest in participating (26.7%), as compared to white (65.8%) and Hispanic/Latinx (71.4%) individuals. Of 115 respondents who expressed interest, 9 enrolled in the clinical trial, which included 6 black, 3 white, and 1 Hispanic/Latinx. During phone outreach to nonresponders and decliners, common reasons for declining included mistrust of the COVID-19 vaccine, underlying health conditions, and logistical barriers to trial participation. Because of low rates of patient portal account activation and use, compounded with vaccine hesitancy, this method yielded a small number of interested individuals. Oxford University Press 2022-11-08 /pmc/articles/PMC9642328/ /pubmed/36380851 http://dx.doi.org/10.1093/jamiaopen/ooac091 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the American Medical Informatics Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Communications Yuh, Tiffany Srivastava, Tuhina Fiore, Danielle Schmidt, Harald Frank, Ian Metzger, David Momplaisir, Florence Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials |
title | Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials |
title_full | Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials |
title_fullStr | Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials |
title_full_unstemmed | Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials |
title_short | Using a patient portal as a recruitment tool to diversify the pool of participants in COVID-19 vaccine clinical trials |
title_sort | using a patient portal as a recruitment tool to diversify the pool of participants in covid-19 vaccine clinical trials |
topic | Brief Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642328/ https://www.ncbi.nlm.nih.gov/pubmed/36380851 http://dx.doi.org/10.1093/jamiaopen/ooac091 |
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