Menu
Recruiting NCT06930404

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

— Observational Obstructive Sleep Apnea (OSA)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: facial scans, videos and heart rate variability measurements.
Who it may be relevant to
Registry conditions: Obstructive Sleep Apnea (OSA). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Australia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

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

Overview

This study will collect data on a range of signals such as facial scans, videos (including speaking, blinking and swallowing) and heart rate variability to assess whether any of these measures are useful for diagnosing obstructive sleep apnea

Interventions

  • Other facial scans, videos and heart rate variability measurements
    Ignite app to collect data (videos, photos and heart rate variability)

Primary outcome measures

  • Correlation of measurement and obstructive sleep apnea status [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

Adults aged >= 18 Ability to read and comprehend English

Exclusion criteria

  • Previous diagnosis of OSA
  • Respiratory diseases (such COPD, lung cancer, fibrosis of the lungs, lung injury)
  • Subjects who are or may be pregnant, breastfeeding or within 6 weeks postpartum (which may impact HRV temporarily)
  • Subjects with a pacemaker

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Australia · 1 center
  • Resmed Sleep Clinic, Bella Vista — Sydney

Identifiers

NCT: NCT06930404 · MA08042025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗