N/A
Completed N=15
Remote Monitoring Use In Cases Of Suspected COVID-19 (Coronavirus)
Coronavirus
Source: ClinicalTrials.gov NCT04337489 ↗
Enrolled (actual)
15
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcomePrimary: Deterioration Resulting in Healthcare Review — 10 alerts generated
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Deterioration Resulting in Healthcare Review |
10 | — |
| SECONDARY Hospitalisation |
— | — |
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.
Data sourced from ClinicalTrials.gov (NCT04337489). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.