Deploy wearable COVID sensor to collect high resolution physiological data (temperature, cardiac, respiratory and physical activity) from COVID positive patients.
Use collected data to train algorithm for assessing the risk of individuals presenting with symptoms suggestive of COVID-19.
Enrollment
550 estimated patients
Sex
All
Ages
18 to 95 years old
Volunteers
Accepts Healthy Volunteers
Inclusion criteria
Ages between 18-95 years old
Currently experiencing any COVID-like signs and symptoms such as fever, cough, shortness of breath, trouble breathing, persistent pain or pressure in the chest, confusion or inability to arouse, bluish lips or face.
Individuals who are not experiencing any COVID like signs and symptoms (will be asked to be healthy control)
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.
Trial design
550 participants in 2 patient groups
COVID-19
Description:
Individuals experiencing COVID-19 like symptoms.
Treatment:
Device: ANNE Sensor
Healthy Controls
Description:
Individuals without any known significant health problems