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Engaging communities in therapeutics clinical research during pandemics: Experiences and lessons from the ACTIV COVID-19 therapeutics research initiative

Published online by Cambridge University Press:  15 October 2024

David A. Wohl
Affiliation:
Institute of Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, NC, USA
Stacey J. Adam*
Affiliation:
Foundation for the National Institutes of Health, Bethesda, MD, USA
Kevin W. Gibbs
Affiliation:
Wake Forest University School of Medicine, Winston-Salem, NC, USA
Ari L. Moskowitz
Affiliation:
Montefiore Medical Center, New York, NY, USA
Thomas L. Ortel
Affiliation:
Departments of Medicine and Pathology, Duke University, Durham, NC, USA
Upinder Singh
Affiliation:
Stanford University, Stanford, CA, USA
Nikolaus Jilg
Affiliation:
Division of Infectious Diseases, Massachusetts General Hospital, and Division of Infectious Diseases, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
Teresa H. Evering
Affiliation:
Weill Cornell Medicine, New York, NY, USA
William A. Fischer II
Affiliation:
Division of Pulmonary Diseases and Critical Care Medicine, University of North Carolina, Chapel Hill, NC, USA
Babafemi O. Taiwo
Affiliation:
Northwestern University, Chicago, IL, USA
Eric S. Daar
Affiliation:
Division of HIV Medicine, Lundquist Institute at Harbor, University of California Los Angeles Medical Center, Los Angeles, CA, USA
Christopher J. Lindsell
Affiliation:
Department of Biostatistics and Bioinformatics, Duke University, Durham, NC, USA Duke Clinical Research Institute, Durham, NC, USA
Susanna Naggie
Affiliation:
Department of Medicine, Duke University, Durham, NC, USA Duke Clinical Research Institute, Durham, NC, USA
Russell L. Rothman
Affiliation:
Vanderbilt University, Nashville, TN, USA
Sarah E. Dunsmore
Affiliation:
National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA
M. Patricia McAdams
Affiliation:
Duke Clinical Research Institute, Durham, NC, USA
Julia Vail
Affiliation:
Duke Clinical Research Institute, Durham, NC, USA
Dushyantha Jayaweera
Affiliation:
Division of Infectious Diseases, Miller School of Medicine, University of Miami, Miami, FL, USA
*
Corresponding author: S. J. Adam; Email: stacey.adam@nih.gov
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Abstract

This manuscript addresses a critical topic: navigating complexities of conducting clinical trials during a pandemic. Central to this discussion is engaging communities to ensure diverse participation. The manuscript elucidates deliberate strategies employed to recruit minority communities with poor social drivers of health for participation in COVID-19 trials. The paper adopts a descriptive approach, eschewing analysis of data-driven efficacy of these efforts, and instead provides a comprehensive account of strategies utilized. The Accelerate COVID-19 Treatment Interventions and Vaccines (ACTIV) public–private partnership launched early in the COVID-19 pandemic to develop clinical trials to advance SARS-CoV-2 treatments. In this paper, ACTIV investigators share challenges in conducting research during an evolving pandemic and approaches selected to engage communities when traditional strategies were infeasible. Lessons from this experience include importance of community representatives’ involvement early in study design and implementation and integration of well-developed public outreach and communication strategies with trial launch. Centralization and coordination of outreach will allow for efficient use of resources and the sharing of best practices. Insights gleaned from the ACTIV program, as outlined in this paper, shed light on effective strategies for involving communities in treatment trials amidst rapidly evolving public health emergencies. This underscores critical importance of community engagement initiatives well in advance of the pandemic.

Information

Type
Review Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of Association for Clinical and Translational Science
Figure 0

Figure 1. Map of ACTIV US sites. This map reflects the locations and geographic distribution of the sites for each of the ACTIV master protocol networks. It should be noted that some trials had deep site representation in areas of classically underserved communities, including those serving African American/Black, Hispanic/Latino, American Indian/Alaskan, and Hawaiian Native. While some trials did not have as deep of coverage, all ACTIV trial networks were very geographically diverse in the USA.

Figure 1

Table 1. Summary of ACTIV therapeutics master protocols recruitment strategies and geographic reach. The 11 ACTIV master protocols tested 37 single agents or combinations, and a summary of the trials and agents can be found in the ACTIV Overview report in this edition. In addition to the primary recruitment strategy for the trials, direct outreach to potential participants by the sites (i.e., data pulls of recent clinic visitors that broadly met inclusion criteria and phone (outpatient) and/or in person (inpatient) recruitment), this table summarizes the important information related to recruitment and geographic coverage of the trials, which helps explain the trials’ demographic makeup. However, unfortunately due to variable start and completion dates of the trials, nonuniform inclusion/exclusion criteria, differential routes of agent administration, and separate trial designs (traditional vs. decentralized), there are too many variables to attribute the variation in recruitment to only the variation in recruitment and outreach strategies. A more thorough comparison of methodologies would need to be tested in a more controlled experiment

Figure 2

Table 2. Challenges to recruitment to ACTIV COVID-19 therapeutics trials. Based on the opinion of the ACTIV investigators in the writing committees

Figure 3

Table 3. ACTIV therapeutics community engagement and outreach response

Figure 4

Figure 2. National Institutes of Health Community Engagement Alliance (CEAL) footprint within the USA. This is the current presence of all of the CEAL activities. Map is from this website: https://nihceal.org/about-community-engaged-research-and-ceal, where more information can be found about CEAL efforts. For purposes of reference, only the original CEAL Regional Teams were present and assisting ACTIV during much of the pandemic. CEAL = Community Engagement Alliance, NIH = National Institutes of Health.

Figure 5

Figure 3. Countries participating in ACTIV trial enrollment globally.

Figure 6

Table 4. ACTIV trial demographics. These trial demographics represent the final trial demographics for all ACTIV master protocols except, ACTIV-2D and ACTIV-4HT, who did not have their final by the time of submission. The demographics also are inclusive of global trial populations for those trials that recruited both in the USA and outside the USA (see Fig. 4 for global distribution of ACTIV trials.) The trial demographics show that while the ACTIV trials did succeed in recruiting populations that are more diverse that most therapeutic trials submitted to the FDA pre-pandemic, not all trials achieved full representativeness of the populations infected with COVID-19

Figure 7

Figure 4. Overarching lessons learned from ACTIV engagement and recruitment activities applicable to future public emergencies. IDeA = Institutional Development Award; PHE = Public Health Emergency.

Figure 8

Table 5. Recommendations for participant outreach, engagement, and recruitment for the next Public Health Emergency

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