Mixed Methods Evaluation of a Novel Apnoea Event Detection Monitor

Status Completed

Clinical Trial Summary

This investigation is looking at a currently available technology to see if it could have another use i.e. in helping to diagnose patients with sleep apnoea.

With 2-4% of the population suffering from this disease, and the current wait time for a test at approximately 20 weeks, it is hoped that a simple screening method could help speed up the process of finding these patients and getting them on treatment faster.

The current standard of care test involves a sleep study in the patients own home with a device with multiple parts and wires. The RespiraSense Sleep Screener is completely cableless and consists of one small, discrete unit attached to the patients side and a mobile device plugged in by the bed.

Patients at Queen Alexandra Hospital who are prescribed sleep studies will be invited to participate. The RespiraSense Sleep Screener data is only for comparison purposes and will have no effect on their clinical care.

If patients agree to participate they will undergo the sleep study with both devices in the same night and may be followed up with over the phone on their experiences with the test.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Respiratory Rate

Clinical Trial Details

NCT number	NCT03149744
Study type	Observational
Source	PMD Solutions
Contact
Status	Completed
Phase
Start date	February 28, 2017
Completion date	May 2, 2017

View Details

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