1. Deploy wearable COVID sensor to collect high resolution physiological data (temperature, cardiac, respiratory and physical activity) from COVID positive patients. 2. Use collected data to train algorithm for assessing the risk of individuals presenting with symptoms suggestive of COVID-19.
Not Provided
Device: ANNE Sensor
The data collected from this sensor contains a wide range of core and novel respiratory
digital biomarkers as a home-based early identification system. The core measurements
include: heart rate, heart rate variability, temperature, physical activity (including
sleep quality) and respiratory rate. The novel respiratory digital biomarkers include:
respiratory cadence (expiration / inspiration time), coughing, swallowing, throat
clearing, and talk time.
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.
Lifepoint Multi-Specialty Hospital
Pune, Maharashtra, India
St. Georges Hospital
Mumbai, Maharastra, India
Induss Hospitals
Hyderabad, Telangana, India
Arun Jayaraman, PT, PhD, Principal Investigator
Shirley Ryan AbilityLab