Obstructive Sleep Apnea (OSA)IgniteNCT06930404
Data Collection Study to Review Novel Methods for Diagnosing Obstructive Sleep Apnea
An observational study of Obstructive Sleep Apnea (OSA), run by ResMed at 1 site in Australia.
Trial 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 Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Obstructive Sleep Apnea (OSA)
- What is being tested?
- facial scans, videos and heart rate variability measurements
- How many people
- 800 participants
- Where
- 1 siteAustralia
- Study dates
- 15 Sep 2025to 15 Feb 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Adults who are being tested for obstructive sleep apnea
Who may be able to join
- Adults aged >= 18 Ability to read and comprehend English
Who cannot join
- 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 locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Australia1 site, 1 recruiting
- Recruiting
Resmed Sleep Clinic, Bella Vista
Sydney, New South Wales, 2153
Alison Wimms, PhD, 0466015420, alison.wimms@resmed.com
About this study
Official title: Innovation and Growth Network for Insightful Trends and Evaluation - Data Collection Study
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
- Conditions
- Obstructive Sleep Apnea (OSA)
- Being tested
- facial scans, videos and heart rate variability measurements
- Keywords
- diagnosis, screening
- Medical subject headings
- Sleep Apnea, Obstructive, Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
facial scans, videos and heart rate variability measurementsOther
Ignite app to collect data (videos, photos and heart rate variability)
| Study group | Role | What they receive |
|---|---|---|
| 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 Receives: Other: facial scans, videos and heart rate variability measurements |
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlation of measurement and obstructive sleep apnea status
- Area under the ROC curve (AUC) for each modality and their combinations in predicting moderate/severe OSA (AHI ≥15).
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Apr 2025
- Study start15 Sep 2025
- Primary completion30 Dec 2026 (estimated)
- Study completion15 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obstructive Sleep Apnea (OSA)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 800 participants (estimated)
Sponsor and investigators
- Lead sponsor
- ResMed
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06930404
- Sponsor's protocol ID
- MA08042025
- Acronym
- Ignite
- Status last verified
- May 2026
- First submitted
- 9 Apr 2025
- Last updated
- 19 May 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 19 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Innovation and Growth Network for Insightful Trends and Evaluation - Data Collection Study
- ClinicalTrials.gov ID
- NCT06930404
- Acronym / sponsor ID
- Ignite / MA08042025
- Conditions
- Obstructive Sleep Apnea (OSA)
- Keywords
- diagnosis, screening
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 800 participants (estimated)
- Lead sponsor
- ResMedIndustry (pharma, biotech, devices)
- Study start
- 15 Sep 2025 (actual)
- Primary completion
- 30 Dec 2026 (estimated)
- Study completion
- 15 Feb 2027 (estimated)
- First posted
- 16 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| People being investigated for obstructive sleep apnea | – | Other: facial scans, videos and heart rate variability measurementsPeople who are undergoing testing (home sleep testing or polysomnography) due to suspicion of sleep apnea will be invited to take part |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Adults who are being tested for obstructive sleep apnea
Key inclusion criteria (1 listed)
- Adults aged >= 18 Ability to read and comprehend English
Key exclusion criteria (4 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| facial scans, videos and heart rate variability measurementsIgnite app to collect data (videos, photos and heart rate variability) | Other | People being investigated for obstructive sleep apnea |
Primary outcome
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).
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 May 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Obstructive Sleep Apnea (OSA), run by ResMed at 1 site in Australia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 19 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Australia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Alison Wimms, PhD (+61466015420, alison.wimms@resmed.com.au), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Correlation of measurement and obstructive sleep apnea status (time frame: 1 day). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 May 2026.