SnoringNCT07097597
Validation of a Snoring App Against Commercially Available Applications and PSG
An observational study of Snoring and Obstructive Sleep Apnea (OSA), run by Windsor Sleep Disorders Clinic.
Trial summary
This study will compare the output of a new snoring application against another commercially available application and polysomnography (either home or in-laboratory). Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Snoring, Obstructive Sleep Apnea (OSA)
- What is being tested?
- Comparison 1: New Snoring Application, Comparison 2: Commercially Available Snoring Application and Comparison 3: Polysomnography
- Type of treatment
- Medical device
- How many people
- 60 participants
- Where
- No sites listed yet
- Study dates
- 1 Sep 2025to 31 Jan 2026
- 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: Patients referred for a diagnostic sleep study at the Windsor Sleep Disorders Clinic
Who may be able to join
- Referred for a diagnostic sleep study
Who cannot join
- Under the age of 18
About this study
Official title: Clinical Validation of a Snoring-App Compared to a Sleep Study and a Commercially Available Application
This study will compare the output of a new snoring application against another commercially available application and polysomnography (either home or in-laboratory).
- Conditions
- Snoring, Obstructive Sleep Apnea (OSA)
- Being tested
- Comparison 1: New Snoring Application, Comparison 2: Commercially Available Snoring Application, Comparison 3: Polysomnography
- Medical subject headings
- Snoring, Sleep Apnea, Obstructive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Comparison 1: New Snoring ApplicationDevice
Measurements obtained from the snoring application under development
Comparison 2: Commercially Available Snoring ApplicationDevice
Measurements from a commercially available snoring application
Comparison 3: PolysomnographyDevice
Measures taken from home or in laboratory polysomnography
| Study group | Role | What they receive |
|---|---|---|
| Sleep Laboratory Patients | Not described Receives: Device: Comparison 1: New Snoring Application; Device: Comparison 2: Commercially Available Snoring Application; Device: Comparison 3: Polysomnography |
What is being measured
The primary outcome is the main question the study is designed to answer.
Snoring
Objective Measurements of snoring intensity (decibel)
Measured: 1 Night recording with all 3 devices
Apneas
Frequency of Apneas (events per hour)
Measured: 1 Night recording with all 3 devices
Snoring
Frequency of snoring (counts)
Measured: 1 Night recording with all 3 devices
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Jul 2025
- Study start1 Sep 2025 (estimated)
- Primary completion31 Jan 2026 (estimated)
- Study completion31 Jan 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SnoringStudies 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
- Cross-sectional
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Windsor Sleep Disorders Clinic
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07097597
- Sponsor's protocol ID
- ValidationSnoringApp
- Status last verified
- Jul 2025
- First submitted
- 16 Jul 2025
- Last updated
- 31 Jul 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 31 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Validation of a Snoring-App Compared to a Sleep Study and a Commercially Available Application
- ClinicalTrials.gov ID
- NCT07097597
- Acronym / sponsor ID
- ValidationSnoringApp
- Conditions
- Snoring, Obstructive Sleep Apnea (OSA)
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Windsor Sleep Disorders ClinicUniversity, hospital or other
- Study start
- 1 Sep 2025 (estimated)
- Primary completion
- 31 Jan 2026 (estimated)
- Study completion
- 31 Jan 2026 (estimated)
- First posted
- 31 Jul 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 compare the output of a new snoring application against another commercially available application and polysomnography (either home or in-laboratory).
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Sleep Laboratory Patients | – | Device: Comparison 1: New Snoring Application, Device: Comparison 2: Commercially Available Snoring Application, Device: Comparison 3: Polysomnography |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Patients referred for a diagnostic sleep study at the Windsor Sleep Disorders Clinic
Key inclusion criteria (1 listed)
- Referred for a diagnostic sleep study
Key exclusion criteria (1 listed)
- Under the age of 18
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 |
|---|---|---|
| Comparison 1: New Snoring ApplicationMeasurements obtained from the snoring application under development | Device | Sleep Laboratory Patients |
| Comparison 2: Commercially Available Snoring ApplicationMeasurements from a commercially available snoring application | Device | Sleep Laboratory Patients |
| Comparison 3: PolysomnographyMeasures taken from home or in laboratory polysomnography | Device | Sleep Laboratory Patients |
Primary outcome
Snoring
Time frame: 1 Night recording with all 3 devices
Objective Measurements of snoring intensity (decibel)
Apneas
Time frame: 1 Night recording with all 3 devices
Frequency of Apneas (events per hour)
Snoring
Time frame: 1 Night recording with all 3 devices
Frequency of snoring (counts)
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 31 Jul 2025.
Related trials for Snoring
RecruitingPhase 3
A Study to Learn About the Monthly Dosing Study Medicine Called Berobenatide in Adults With Breathing Problems During Sleep and Overweight or Obesity Who Do Not Use a Breathing Machine (PAP) (VESPER-OSA 2)
Apnea, Sleep Disorders
RecruitingObservational study
Prediction of Tongue Base Obstruction During Sleep
Obstructive Sleep Disordered Breathing
Active, not recruiting
The Impact of Technology in Obstructive Sleep Apnea Myofunctional Therapy
Obstructive Sleep Apnea (OSA), Snoring
Active, not recruiting
DISE: Phenotyping Obstruction Patterns
Obstructive Sleep Apnea
RecruitingPhase 1
Use of Passive Myofunctional Appliances for Snoring and Mild Obstructive Sleep Apnea
Sleep Apnea, Obstructive
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.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Snoring and Obstructive Sleep Apnea (OSA), run by Windsor Sleep Disorders Clinic.
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 1 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: opening soon, as of the sponsor's last update on 31 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.
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?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Snoring (time frame: 1 Night recording with all 3 devices). The study lists 3 primary outcomes in all. 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 31 Jul 2025.