Remote Monitoring Use In Cases Of Suspected COVID-19 (Coronavirus)

Imperial College London15 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Coronavirus

Interventions

SensiumVitals wearable sensorDEVICE

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

Eligibility

Sex: ALLMin age: 18 YearsMax age: 95 Years

Medical Language ↔ Plain English

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.

Locations (1)

Imperial College London

London, United Kingdom

Outcomes

Primary Outcomes

Deterioration Resulting in Healthcare Review

Detection of clinical deterioration using wearable sensors resulting in healthcare review (e.g. GP telephone consultation)

Time frame: 1 year

Secondary Outcomes

Hospitalisation

Deterioration resulting in hospitalisation

Time frame: 1 year

Data from ClinicalTrials.gov

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