Monitoring heart rate, respiration, and sleep using an under-mattress device

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.