Diversity and inclusion for the All of Us research program: A scoping review
Year: 2020
Type: article
Abstract: The All of Us Research Program (All of Us) is a national effort to accelerate health research by exploring the relationship between lifestyle, environment, and genetics. It is set to become one of the largest research efforts in U.S. history, aiming to build a national resource of data from at least one million participants. All of Us aims to address the need for more diversity in research and set the stage for that diversity to be leveraged in precision medicine research to come. This paper describes how the program assessed demographic characteristics of participants who have enrolled in other U.S. biomedical research cohorts to better understand which groups are traditionally represented or underrepresented in biomedical research. We 1) reviewed the enrollment characteristics of national cohort studies like All of Us, and 2) surveyed the literature, focusing on key diversity categories essential to the program's enrollment aims. Based on these efforts, All of Us emphasizes enrollment of racial and ethnic minorities, and has formally designated the following additional groups as historically underrepresented: individuals-with inadequate access to medical care; under the age of 18 or over 65; with an annual household income at or below 200% of the federal poverty level; who have a cognitive or physical disability; have less than a high school education or equivalent; are intersex; identify as a sexual or gender minority; or live in rural or non-metropolitan areas. Research accounting for wider demographic variability is critical. Only by ensuring diversity and by addressing the very barriers that limit it, can we position All of Us to better understand and tackle health disparities.
Source: PLoS ONE
Institutions: Vanderbilt University Medical Center, National Institutes of Health, Office of the Director, Scripps Health, Scripps Whittier Diabetes Institute, Massachusetts Institute of Technology, National Institute on Minority Health and Health Disparities, National Center for Advancing Translational Sciences
Language: English
Topic: Ethics in Clinical Research
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,695
Awards: G2054976188, G3400831664, Using Patient-Centered Guidelines in a Technology Platform to Improve Health Care in Adults with Sickle Cell Disease, PMI Participants Preparatory/Prototyping Initiative, G4907731533, Technology to Empower Changes in Health (TECH) Network Participant Technologies Center, Data and Research Support Center , Scripps Translational Science Institute
OpenAlex ID: W3038167169
