Actively Recruiting
Detecting Heart Rate, Respiration, and Sleep With the Sleeptracker-AI Under-mattress Monitor
Led by Woolcock Institute of Medical Research · Updated on 2025-03-28
100
Participants Needed
1
Research Sites
153 weeks
Total Duration
On this page
Sponsors
W
Woolcock Institute of Medical Research
Lead Sponsor
F
Fullpower Technologies, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the Sleeptracker-AI Monitor, an under-mattress device that records sleep and breathing data, in patients undergoing routine overnight sleep studies at the Woolcock Institute for possible obstructive sleep apnea (OSA). This observational study aims to collect simultaneous data from the Sleeptracker device and standard polysomnography (PSG) to improve the Sleeptracker's algorithms for detecting sleep and breathing disorders. The data collected will be de-identified to protect patient privacy. Participants will use the Sleeptracker-AI Monitor, which is a non-wearable, commercially available device placed under the mattress. It uses sensors to detect movements, heartbeats, respiration, and snoring vibrations during sleep. The study involves no additional treatment but focuses on data collection during the participant's routine PSG sleep study. The de-identified data from the Sleeptracker and PSG will be uploaded securely to help refine the device's detection algorithms. During the study, participants will undergo standard overnight PSG testing while the Sleeptracker device simultaneously records data. Researchers will measure the Apnea Hypopnea Index as the primary outcome and assess total sleep time, NREM sleep time, and REM sleep time as secondary outcomes. The study includes adults aged 20 to 90 years and will continue until October 2028. Participants' involvement consists mainly of consenting to data collection during their scheduled sleep study, with no extra procedures or follow-up visits required.
CONDITIONS
Brief Title
Detecting Heart Rate, Respiration, and Sleep With the Sleeptracker-AI Under-mattress Monitor
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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.
You will not qualify if you...
- Unable to understand study procedure.
- Unable to sign informed consent form.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 night
Participants undergo an overnight polysomnography (PSG) sleep study while simultaneously using the Sleeptracker-AI Monitor placed under the mattress to collect sleep and breathing data.
1 overnight visit (in-person)
Duration - Up to study completion
De-identified data from the Sleeptracker device and PSG are uploaded and used to improve algorithms for detecting sleep and breathing disturbances.
No additional visits required
Trial Site Locations
Total: 1 location
1
Woolcock Institute of Medical Research
Macquarie Park, New South Wales, Australia, 2113
Actively Recruiting
Research Team
C
Camillah Hoyos, PhD
C
Craig L Phillips, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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