Official Title
REmote MOniToring usE in Suspected Cases of COVID-19 (Coronavirus): REMOTE-COVID Trial
Brief Summary

The study aims to see if participant deterioration due to suspected coronavirus in a designated location (e.g. hotel) can be identified sooner by wearing the sensor. If sick patients can be identified early, participants are more likely to have better outcomes; the study believes that the sensor can help us do this. The sensor measures heart rate, respiratory rate and temperature every 2 minutes and this can be reviewed by the clinical team looking after the participants.

Completed
Coronavirus

Device: SensiumVitals wearable sensor

A waterproof, light, wearable sensor measuring vital signs (heart rate, respiratory rate, temperature) continuously.

Eligibility Criteria

Inclusion Criteria:

- Aged 18 years or over.

- Able to provide written consent.

Exclusion Criteria:

- Any participants that withdraw their consent.

- A skin condition/reaction preventing wearing the wearable sensor.

- The presence of a permanent pacemaker or cardiac defibrillator.

- Any form of psychiatric disorder or a condition that, in the opinion of the
investigator, may hinder communication with the research team.

- Inability to cooperate or communicate with the research team.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 95 Years
Countries
United Kingdom
Locations

Imperial College London
London, United Kingdom

Ara Darzi, Prof, Principal Investigator
Institute of Global Health Innovation

NCT Number
Keywords
Coronavirus
remote monitoring
deterioration
escalation
MeSH Terms
Coronavirus Infections