Title
A risk assessment tool for resumption of research activities during the COVID-19 pandemic for field trials in low resource settings
Date Issued
01 December 2021
Access level
open access
Resource Type
journal article
Author(s)
Simkovich S.M.
Thompson L.M.
Clark M.L.
Balakrishnan K.
Checkley W.
Clasen T.
Davila-Roman V.G.
Diaz-Artiga A.
Dusabimana E.
Fuentes L.d.l.
Harvey S.
Kirby M.A.
Lovvorn A.
McCollum E.D.
Mollinedo E.E.
Peel J.L.
Quinn A.
Rosa G.
Underhill L.J.
Young B.N.
Rosenthal J.
Aravindalochanan V.
Barr D.B.
Burrowes V.
Campbell D.
Campbell J.M.P.
Canuz E.
Castañaza A.
Chang H.
Chen Y.
Craik R.
Crocker M.
Dávila-Román V.
De Léon O.
Diaz-Artiga A.
Elon L.
Espinoza J.G.
Fuentes I.S.P.
Garg S.
Goodman D.
Gupton S.
Hardison M.
Harvey S.A.
Hengstermann M.
Herrera P.
Hossen S.
Howards P.
Jaacks L.
Jabbarzadeh S.
Johnson M.A.
Jones A.
Kearns K.
Kirby M.
Kremer J.
Laws M.
Lenzen P.M.
Liao J.
Majorin F.
McCollum E.
McCracken J.P.
Meyers R.M.
Mollinedo E.E.
Moulton L.
Mukhopadhyay K.
Naeher L.
Nambajimana A.
Ndagijimana F.
Nizam A.
de Dieu Ntivuguruzwa J.
Papageorghiou A.
Peel J.L.
Piedrahita R.
Pillarisetti A.
Puttaswamy N.
Puzzolo E.
Rajkumar S.
Ramakrishnan U.
Reardon D.
Ryan P.B.
Sakas Z.
Sambandam S.
Sarnat J.
Simkovich S.M.
Sinharoy S.
Smith K.R.
Steenland K.
Swearing D.
Thangavel G.
Toenjes A.K.
Underhill L.
Uwizeyimana J.D.
Valdes V.
Verma A.
Waller L.
Warnock M.
Publisher(s)
BioMed Central Ltd
Abstract
Rationale: The spread of severe acute respiratory syndrome coronavirus-2 has suspended many non-COVID-19 related research activities. Where restarting research activities is permitted, investigators need to evaluate the risks and benefits of resuming data collection and adapt procedures to minimize risk. Objectives: In the context of the multicountry Household Air Pollution Intervention (HAPIN) trial conducted in rural, low-resource settings, we developed a framework to assess the risk of each trial activity and to guide protective measures. Our goal is to maximize the integrity of reseach aims while minimizing infection risk based on the latest scientific understanding of the virus. Methods: We drew on a combination of expert consultations, risk assessment frameworks, institutional guidance and literature to develop our framework. We then systematically graded clinical, behavioral, laboratory and field environmental health research activities in four countries for both adult and child subjects using this framework. National and local government recommendations provided the minimum safety guidelines for our work. Results: Our framework assesses risk based on staff proximity to the participant, exposure time between staff and participants, and potential viral aerosolization while performing the activity. For each activity, one of four risk levels, from minimal to unacceptable, is assigned and guidance on protective measures is provided. Those activities that can potentially aerosolize the virus are deemed the highest risk. Conclusions: By applying a systematic, procedure-specific approach to risk assessment for each trial activity, we were able to protect our participants and research team and to uphold our ability to deliver on the research commitments we have made to our staff, participants, local communities, and funders. This framework can be tailored to other research studies conducted in similar settings during the current pandemic, as well as potential future outbreaks with similar transmission dynamics. The trial is registered with clinicaltrials.gov NCT02944682 on October 26. 2016.
Volume
21
Issue
1
Language
English
OCDE Knowledge area
Epidemiología
Subjects
Scopus EID
2-s2.0-85104346553
PubMed ID
Source
BMC Medical Research Methodology
ISSN of the container
14712288
Sponsor(s)
This study is funded by the U.S. National Institutes of Health (cooperative agreement 1UM1HL134590) in collaboration with the Bill & Melinda Gates Foundation (OPP1131279). Participating NIH organizations include the National Heart, Lung and Blood Institute, National Institute of Environmental Health Sciences, National Cancer Institute, National Institute of Child Health and Human Development, Fogarty International Center, and the NIH Common Fund. Suzanne M. Simkovich was supported by funding from the National Heart, Lung and Blood Institute U., the National Heart, Lung, and Blood Institute 1F32HL143909–01, the National Heart, Lung, and Blood Institute K12HL137942. Lindsay J. Underhill and Kendra Williams were supported by Research Training Grant D43TW009340 (MPIs: Buekens, Checkley, Chi, Kondwani) funded by United States National Institutes of Health through the following Institutes and Centers: Fogarty International Center, National Institute of Neurological Disorders and Stroke, National Institute of Mental Health, National Heart, Lung, and Blood Institute and the National Institute of Environmental Health Sciences along with the National Heart, Lung, and Blood Institute 1F32HL143909–01.
Program Coordination: Gail Rodgers, M.D., Bill & Melinda Gates Foundation; Claudia L. Thompson, Ph.D., National Institute of Environmental Health Science (NIEHS); Mark J. Parascandola, Ph.D., M.P.H., National Cancer Institute (NCI); Danuta M. Krotoski, Ph.D., Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD); Joshua P. Rosenthal, Ph.D., Fogarty International Center (FIC); Conception R. Nierras, Ph.D., NIH Office of Strategic Coordination Common Fund; Antonello Punturieri, M.D., Ph.D. and Barry S. Schmetter, B.S., National Heart, Lung, and Blood Institute (NHLBI).
Sources of information:
Directorio de Producción Científica
Scopus