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

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

15 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-07-28

Study Completion Date

2021-03-26

Brief Summary

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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.

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Detailed Description

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Conditions

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Coronavirus

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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SensiumVitals wearable sensor

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

Intervention Type DEVICE

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

95 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No