Diversity and Inclusion in Unregulated mHealth Research: Addressing the Risks.

J Law Med Ethics

Shawneequa Callier, M.A., J.D., is an Associate Professor of Clinical Research and Leadership in the Department of Clinical Research and Leadership at the School of Medicine and Health Sciences at The George Washington University in Washington, D.C. She is also a Special Volunteer at the Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health. Stephanie M. Fullerton, D.Phil., is a Professor in the Department of Bioethics and Humanities at the University of Washington School of Medicine in Seattle, WA.

Published: March 2020

mHealth devices and applications, with their wide accessibility and ease of use, have the potential to address persistent inequities in biomedical research participation. Yet, while mHealth technologies may facilitate more inclusive research participation, negative features of some unregulated use in research - misleading enrollment practices, the promotion of secondary mHealth applications, discriminatory profiling, and poorer quality feedback due to dependencies on biased data and algorithms - may threaten the trust and engagement of underrepresented individuals and communities. To maximize the participation of currently disenfranchised groups, those involved in unregulated mHealth research must become aware of potential risks, adopt targeted education policies, audit algorithms for hidden biases, and engage citizen scientists and other community members to identify and forestall possible harms.

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Source
http://dx.doi.org/10.1177/1073110520917036DOI Listing

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