This study will monitor physical bio-markers such as heart rate, respiratory rate, and temperature to detect potential COVID-19 infections.



Eligible Ages
Over 18 Years
Eligible Genders
Accepts Healthy Volunteers

Inclusion Criteria

  • Adults aged 18 years old or over - Recent (within 1 week) occupational or home exposure to a newly diagnosed COVID-19 infected individual - Able and willing to give written consent and comply with study procedures

Exclusion Criteria

  • Inability to understand instructions and follow a three step command - The subject is pregnant, nursing or planning a pregnancy - Inability to provide written consent - Past confirmed COVID-19 infection with resolution of symptoms - Past confirmed COVID-19 active infection moderate or severe symptoms

Study Design

Study Type
Observational Model
Time Perspective

Arm Groups

ArmDescriptionAssigned Intervention
Healthy Adults Adults 18 years or older
  • Device: ANNE One
    Wireless vital sign monitoring device
COVID19 Adults 18 years or older diagnosed with COVID 19
  • Device: ANNE One
    Wireless vital sign monitoring device

Recruiting Locations

More Details

Active, not recruiting
Northwestern University

Detailed Description

The purpose of this research is to assess the accuracy of wearable sensors at detecting and monitoring COVID-19 infections. Our small, wearable sensor can get data on your respiration, body temperature, heart rate, and blood oxygen level, which may help physicians better identify if a respiratory condition is worsening overtime. If successful, our sensor could help healthcare professionals detect early symptoms of COVID-19 respiratory infection and monitor recovery and treat people before their condition worsens significantly.


Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.