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

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ResMed

Status

Not yet enrolling

Conditions

Obstructive Sleep Apnea (OSA)

Treatments

Other: facial scans, videos and heart rate variability measurements

Study type

Observational

Funder types

Industry

Identifiers

NCT06930404
MA08042025

Details and patient eligibility

About

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

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

300 participants in 1 patient group

People being investigated for obstructive sleep apnea
Description:
People who are undergoing testing (home sleep testing or polysomnography) due to suspicion of sleep apnea will be invited to take part
Treatment:
Other: facial scans, videos and heart rate variability measurements

Trial contacts and locations

0

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Central trial contact

Alison Wimms, PhD

Data sourced from clinicaltrials.gov

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