ABSTRACT
Contact tracing is a crucial process of information exchange in which health institutions share guidance with the public and obtain local health data to curb the spread of disease. But this data collection can exacerbate multiple forms of anxiety, particularly for people who have historically been excluded from and exploited by public health institutions. Given this history, our article centers the perspectives of contact tracers and BIPOC tracees in two US cities: Philadelphia, PA and Providence, RI. Our analysis shows that many BIPOC tracees experience information anxiety, shaped by complex relationships between their communities and health institutions, inconsistent access to care, and privacy concerns. At the same time, contact tracers have the potential to mitigate this anxiety, though this capacity is influenced by the institutional conditions in which they work. By analyzing both tracers’ and tracees’ perspectives on contact tracing, this study contributes grounded and holistic accounts of how public health institutions can better serve local communities, particularly communities of color in urban areas, during public health crises.
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No potential conflict of interest was reported by the author(s).
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Notes on contributors
Jenny Lee
Jenny Lee is a PhD student at the Annenberg School for Communication at the University of Pennsylvania.
Jessa Lingel
Jessa Lingel is an Associate Professor of Communication at the Annenberg School for Communication at the University of Pennsylvania and Core Faculty in the Gender, Sexuality, and Women's Studies department.
Alexandra Sanchez
Alexandra Sanchez is an activist with Free Radicals.
Theo Loftis is an activist with Creative Resilience Collective.
Amelia Mauldin
Amelia Mauldin is a recent graduate of the Annenberg School of Communication at the University of Pennsylvania.