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NCT Number: NCT07097597

Validation of a Snoring App Against Commercially Available Applications and PSG

This study will compare the output of a new snoring application against another commercially available application and polysomnography (either home or in-laboratory).

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Referred for a diagnostic sleep study

Exclusion criteria

  • Under the age of 18

Treatment and study plan

Comparison 1: New Snoring Application

Device

Measurements obtained from the snoring application under development

Comparison 2: Commercially Available Snoring Application

Device

Measurements from a commercially available snoring application

Comparison 3: Polysomnography

Device

Measures taken from home or in laboratory polysomnography

Primary outcomes

  1. Snoring

    Time frame: 1 Night recording with all 3 devices

    Objective Measurements of snoring intensity (decibel)

  2. Apneas

    Time frame: 1 Night recording with all 3 devices

    Frequency of Apneas (events per hour)

  3. Snoring

    Time frame: 1 Night recording with all 3 devices

    Frequency of snoring (counts)

Sponsors and collaborators

Lead sponsor

Windsor Sleep Disorders Clinic

Other

Registry information

Official study title

Clinical Validation of a Snoring-App Compared to a Sleep Study and a Commercially Available Application

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 31, 2025
Registry last updated
Jul 31, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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