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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

  • 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
  • , On behalf of the COVID-RED Consortium
  • *Corresponding author for this work
  • Utrecht University
  • Julius Clinical
  • Ava AG
  • North West University
  • The Institute for Artificial Intelligence of Serbia
  • University of Fribourg
  • Roche Diagnostics Nederland BV
  • Roche
  • VIVE
  • Dr Risch Medical Laboratory
  • Private University in the Principality of Liechtenstein (UFL)
  • University of Bern
  • Population Health Research Institute, Ontario
  • Kantonsspital Graubünden
  • Sanquin Blood Supply Foundation
  • Amsterdam UMC
  • University College London Hospitals NHS Foundation Trust
  • King's College London
  • University College London
  • Sanquin
  • Takeda

Research output: Contribution to journal › Article › Academic › peer-review

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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 - 1 Jun 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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