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Remote early detection of SARS-CoV-2 infections using a wearable-based algorithm: Results from the COVID-RED study, a prospective randomised single-blinded crossover trial

  • COVID-RED consortium
  • , Laura C Zwiers*
  • , Timo B Brakenhoff
  • , Brianna M Goodale
  • , Duco Veen
  • , George S Downward
  • , Vladimir Kovacevic
  • , Andjela Markovic
  • , Marianna Mitratza
  • , Marcel van Willigen
  • , Billy Franks
  • , Janneke van de Wijgert
  • , Santiago Montes
  • , Serkan Korkmaz
  • , Jakob Kjellberg
  • , Lorenz Risch
  • , David Conen
  • , Martin Risch
  • , Kirsten Grossman
  • , Ornella C Weideli
  • Theo Rispens, Jon Bouwman, Amos A Folarin, Xi Bai, Richard Dobson, Maureen Cronin, Diederick E Grobbee
*Corresponding author for this work
  • University Medical Center Utrecht
  • Ava AG
  • Roche Diagnostics Nederland B.V.
  • VIVE
  • Laboratory Dr. Risch
  • McMaster University
  • Sanquin Research and Landsteiner Laboratory
  • University College London

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background Rapid and early detection of SARS-CoV-2 infections, especially during the pre- or asymptomatic phase, could aid in reducing virus spread. Physiological parameters measured by wearable devices can be efficiently analysed to provide early detection of infections. The COVID-19 Remote Early Detection (COVID-RED) trial investigated the use of a wearable device (Ava bracelet) for improved early detection of SARS-CoV-2 infections in real-time. Trial design Prospective, single-blinded, two-period, two-sequence, randomised controlled cross¬over trial. Methods Subjects wore a medical device and synced it with a mobile application in which they also reported symptoms. Subjects in the experimental condition received real-time infection indications based on an algorithm using both wearable device and self-reported symptom data, while subjects in the control arm received indications based on daily symptom-reporting only. Subjects were asked to get tested for SARS-CoV-2 when receiving an app-generated alert, and additionally underwent periodic SARS-CoV-2 serology testing. The overall and early detection performance of both algorithms was evaluated and compared using metrics such as sensitivity and specificity. Results A total of 17,825 subjects were randomised within the study. Subjects in the experimental condition received an alert significantly earlier than those in the con¬trol condition (median of 0 versus 7 days before a positive SARS-CoV-2 test). The experimental algorithm achieved high sensitivity (93.8-99.2%) but low specificity (0.8-4.2%) when detecting infections during a specified period, while the con¬trol algorithm achieved more moderate sensitivity (43.3-46.4%) and specificity (66.4-65.0%). When detecting infection on a given day, the experimental algorithm also achieved higher sensitivity compared to the control algorithm (45-52% versus 28-33%), but much lower specificity (38-50% versus 93-97%). Conclusions Our findings highlight the potential role of wearable devices in early detection of SARS-CoV-2. The experimental algorithm overestimated infections, but future itera¬tions could finetune the algorithm to improve specificity and enable it to differentiate between respiratory illnesses.

Original languageEnglish
Article numbere0325116
JournalPloS one
Volume20
Issue number6 June
DOIs
Publication statusPublished - 5 Jun 2025

Bibliographical note

Publisher Copyright:
© 2025 Zwiers et al.

Funding

The COVID-RED project has received funding from the Innovative Medicines Initiative (https://www.imi.europa.eu) 2 Joint Undertaking under grant agreement No 101005177. This Joint Undertaking receives support from the European Union's Horizon 2020 (https://ec.europa.eu/programmes/hori¬zon2020/) research and innovation programme and EFPIA (https://www.efpia.eu/). Disclaimer: The research leading to these results was con¬ducted as part of the COVID-RED Consortium. This paper only reflects the personal views of the stated authors. The funding body has no role in the design of the study; the collection, analysis, and interpretation of the data; and the writing of the manuscript.

FundersFunder number
Horizon 2020 Framework Programme
European Federation of Pharmaceutical Industries and Associations
Innovative Medicines Initiative101005177

    Keywords

    • Adult
    • Aged
    • Algorithms
    • COVID-19/diagnosis
    • Cross-Over Studies
    • Early Diagnosis
    • Female
    • Humans
    • Male
    • Middle Aged
    • Mobile Applications
    • Prospective Studies
    • SARS-CoV-2/isolation & purification
    • Single-Blind Method
    • Wearable Electronic Devices

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