Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06930404

Innovation and Growth Network for Insightful Trends and Evaluation - Data Collection Study

Led by ResMed · Updated on 2026-05-19

800

Participants Needed

1

Research Sites

6 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are collecting data to explore new ways to diagnose obstructive sleep apnea (OSA). They will study signals such as facial scans, videos showing speaking, blinking, and swallowing, as well as heart rate variability. The goal is to see if any of these measures can help identify OSA in people being tested for this condition. The study is observational and sponsored by ResMed. Participants suspected of having sleep apnea and undergoing home sleep testing or polysomnography will be invited to join. Data collection involves using the Ignite app to capture videos, photos, and heart rate variability measurements. This study focuses on gathering information without providing any treatment. During the study, participants will have their data collected and assessed to find correlations between these measurements and OSA status. The main outcome is to evaluate how well these signals relate to the diagnosis of obstructive sleep apnea. The study will run from September 2025 to February 2027, and participants will be followed for a brief period to complete data collection.

CONDITIONS

Brief Title

Data Collection Study to Review Novel Methods for Diagnosing Obstructive Sleep Apnea

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged �3E= 18
  • Ability to read and comprehend English
Not Eligible

You will not qualify if you...

  • Previous diagnosis of obstructive sleep apnea
  • Respiratory diseases such as COPD, lung cancer, fibrosis of the lungs, or lung injury
  • Currently pregnant, breastfeeding, or within 6 weeks postpartum
  • Presence of a pacemaker

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Diagnostic Evaluation

Duration - 1 day

Participants undergo facial scans, videos, and heart rate variability measurements using the Ignite app to collect data alongside their clinical sleep apnea testing.

1 visit (in-person or remote)

Long-term Monitoring

Duration - Up to several months depending on data analysis timelines

Participants' data is observed and analyzed to correlate measurements with obstructive sleep apnea status.

No scheduled visits

Trial Site Locations

Total: 1 location

1

Resmed Sleep Clinic, Bella Vista

Sydney, New South Wales, Australia, 2153

Actively Recruiting

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Research Team

A

Alison Wimms, 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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