Research on the Epidemiology of SARS-CoV-2 in Essential Response Personnel (RECOVER): Protocol for a Multisite Longitudinal Cohort Study

Laura J. Edwards, Ashley L. Fowlkes, Meredith G. Wesley, Jennifer L. Kuntz, Marilyn J. Odean, Alberto J. Caban-Martinez, Kayan Dunnigan, Andrew L. Phillips, Lauren Grant, Meghan K. Herring, Holly C. Groom, Karley Respet, Shawn Beitel, Tnelda Zunie, Kurt Hegmann, Archana Kumar, Gregory Joseph, Brandon Poe, Paola Louzado-Feliciano, Michael SmithMatthew S. Thiese, Natasha Schaefer-Solle, Young M. Yoo, Carlos A. Silvera, Julie Mayo Lamberte, Josephine Mak, L. Clifford McDonald, Matthew J. Stuckey, Preeta Kutty, Melissa L. Arvay, Sarang K. Yoon, Harmony L. Tyner, Jefferey L. Burgess, Danielle Rentz Hunt, Jennifer Meece, Manjusha Gaglani, Allison L. Naleway, Mark G. Thompson

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Background: Workers critical to emergency response and continuity of essential services during the COVID-19 pandemic are at a disproportionally high risk of SARS-CoV-2 infection. Prospective cohort studies are needed for enhancing the understanding of the incidence of symptomatic and asymptomatic SARS-CoV-2 infections, identifying risk factors, assessing clinical outcomes, and determining the effectiveness of vaccination. Objective: The Research on the Epidemiology of SARS-CoV-2 in Essential Response Personnel (RECOVER) prospective cohort study was designed to estimate the incidence of symptomatic and asymptomatic SARS-CoV-2 infections, examine the risk factors for infection and clinical spectrum of illness, and assess the effectiveness of vaccination among essential workers. Methods: The RECOVER multisite network was initiated in August 2020 and aims to enroll 3000 health care personnel (HCP), first responders, and other essential and frontline workers (EFWs) at 6 US locations. Data on participant demographics, medical history, and vaccination history are collected at baseline and throughout the study. Active surveillance for the symptoms of COVID-19–like illness (CLI), access of medical care, and symptom duration is performed by text messages, emails, and direct participant or medical record reports. Participants self-collect a mid-turbinate nasal swab weekly, regardless of symptoms, and 2 additional respiratory specimens at the onset of CLI. Blood is collected upon enrollment, every 3 months, approximately 28 days after a reverse transcription polymerase chain reaction (RT-PCR)–confirmed SARS-CoV-2 infection, and 14 to 28 days after a dose of any COVID-19 vaccine. From February 2021, household members of RT-PCR–confirmed participants are self-collecting mid-turbinate nasal swabs daily for 10 days. Results: The study observation period began in August 2020 and is expected to continue through spring 2022. There are 2623 actively enrolled RECOVER participants, including 280 participants who have been found to be positive for SARS-CoV-2 by RT-PCR. Enrollment is ongoing at 3 of the 6 study sites. Conclusions: Data collected through the cohort are expected to provide important public health information for essential workers at high risk for occupational exposure to SARS-CoV-2 and allow early evaluation of COVID-19 vaccine effectiveness.

Original languageEnglish (US)
Article numbere31574
JournalJMIR Research Protocols
Volume10
Issue number12
DOIs
StatePublished - Dec 2021

Keywords

  • COVID-19
  • Cohort study
  • Essential
  • First responder
  • Frontline workers
  • Health care personnel
  • Incidence
  • SARS-CoV-2
  • Vaccine effectiveness

ASJC Scopus subject areas

  • Medicine(all)

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