OSA
Conditions
Keywords
validation study, Sleeptracker-AI, polysomnography
Brief summary
The objective of this study is to simultaneously acquire sleep and breathing data using the under-mattress Sleeptracker (The Sleeptracker-AI Monitor (Fullpower Technologies, California, USA) during routine PSGs in patients who attend the Woolcock Institute for undergoing investigation for possible obstructive sleep apnoea (OSA).
Detailed description
The objective of this study is to simultaneously acquire sleep and breathing data using the under-mattress Sleeptracker (The Sleeptracker-AI Monitor (Fullpower Technologies, California, USA) during routine PSGs in patients who attend the Woolcock Institute for undergoing investigation for possible obstructive sleep apnoea (OSA). The de-identified Sleeptracker and PSG data will then be used by Fullpower Technologies to improve the accuracy of their current algorithm for detecting sleep and breathing disorders using the Sleeptracker device. De-identified data recorded from the Sleeptracker device and PSG data from the Compumedics Grael system will be manually uploaded to a secure commercial server maintained by Fullpower Technologies. Fullpower Technologies will use the de-identified data to refine their algorithms for detecting sleep and breathing disturbances.
Interventions
DEVICESleeptracker-AI
The Sleeptracker-AI Monitor (Fullpower Technologies, California, USA) is a commercially available, unobtrusive, and non-wearable home sleep monitoring device. It is either pre-installed in a mattress or can be purchased separately by consumers where it is placed under the mattress. The device uses piezo-electric sensors that register the forces exerted through the mattress by features such as the subject's motion, respiration, heartbeats, and snoring vibrations.
Sponsors
Fullpower Technologies, Inc.
Woolcock Institute of Medical Research
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
20 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* Adults aged 20-90 years old at time of assessment. * Attending the Woolcock Institute for an overnight sleep study for investigation of sleep apnoea. * Able to give informed consent. * Fluent in English.
Exclusion criteria
* Unable to understand study procedure. * Unable to sign informed consent form.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Apnea Hypopnea Index | One night | AHI (events per hour of sleep) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Total Sleep Time | One night | Total Sleep Time (minutes) |
| NREM Sleep Time | One night | Non-REM sleep time (minutes) |
| REM Sleep Time | One night | REM sleep time (minutes) |
Countries
Australia
Contacts
Primary ContactCamillah Hoyos, PhD
Backup ContactCraig L Phillips, PhD
Outcome results
None listed