NCT06930404RecruitingNot Applicable
Innovation and Growth Network for Insightful Trends and Evaluation - Data Collection Study
ResMed1 site in 1 country800 target enrollmentStarted: September 15, 2025Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- Enrollment
- 800
- Locations
- 1
- Primary Endpoint
- Correlation of measurement and obstructive sleep apnea status
Study Overview
Brief Summary
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
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
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
Arms & Interventions
People being investigated for obstructive sleep apnea
People who are undergoing testing (home sleep testing or polysomnography) due to suspicion of sleep apnea will be invited to take part
Intervention: facial scans, videos and heart rate variability measurements (Other)
Outcomes
Primary Outcomes
Correlation of measurement and obstructive sleep apnea status
Time Frame: 1 day
\- Area under the ROC curve (AUC) for each modality and their combinations in predicting moderate/severe OSA (AHI ≥15).
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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