Monitoring heart rate, respiration, and sleep using an under-mattress device
Detecting Heart Rate, Respiration, and Sleep With the Sleeptracker-AI Under-mattress Monitor
Woolcock Institute of Medical Research · NCT06110962
This study is testing a new under-mattress device to see if it can help gather better sleep and breathing information for adults suspected of having sleep apnea during their overnight sleep study.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 20 Years to 90 Years |
| Sex | All |
| Sponsor | Woolcock Institute of Medical Research (other) |
| Locations | 1 site (Macquarie Park, New South Wales) |
| Trial ID | NCT06110962 on ClinicalTrials.gov |
What this trial studies
This study aims to collect sleep and breathing data using the Sleeptracker-AI Monitor during routine polysomnography (PSG) assessments for patients suspected of having obstructive sleep apnea (OSA). The data collected will be de-identified and used by Fullpower Technologies to enhance their algorithms for detecting sleep and breathing disorders. Participants will be adults attending the Woolcock Institute for an overnight sleep study, where both the Sleeptracker and PSG data will be analyzed to improve diagnostic accuracy.
Who should consider this trial
Good fit: Ideal candidates are adults aged 20-90 who are undergoing evaluation for sleep apnea at the Woolcock Institute.
Not a fit: Patients who are unable to understand the study procedures or cannot provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more accurate and non-invasive methods for diagnosing sleep and breathing disorders.
How similar studies have performed: Other studies have shown promise in using technology for sleep monitoring, but the specific application of the Sleeptracker-AI is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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.
Where this trial is running
Macquarie Park, New South Wales
- Woolcock Institute of Medical Research — Macquarie Park, New South Wales, Australia (RECRUITING)
Study contacts
- Principal investigator: Craig Phillips, PhD — Woolcock Institute of Medical Research
- Study coordinator: Camillah Hoyos, PhD
- Email: camilla.hoyos@mq.edu.au
- Phone: +61298053229
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: OSA, validation study, Sleeptracker-AI, polysomnography