Validation of a Snoring App Against Commercially Available Applications and PSG

N/ANot Yet RecruitingNCT07097597

Windsor Sleep Disorders Clinic60 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

Conditions

Snoring Obstructive Sleep Apnea (OSA)

Interventions

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

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Referred for a diagnostic sleep study Exclusion Criteria: * Under the age of 18

Outcomes

Primary Outcomes

Snoring

Objective Measurements of snoring intensity (decibel)

Time frame: 1 Night recording with all 3 devices

Apneas

Frequency of Apneas (events per hour)

Time frame: 1 Night recording with all 3 devices

Snoring

Frequency of snoring (counts)

Time frame: 1 Night recording with all 3 devices

Data from ClinicalTrials.gov

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