Obstructive Sleep Apnea (OSA), Snoring
Conditions
Brief summary
This study will compare the output of a new snoring application against another commercially available application and polysomnography (either home or in-laboratory).
Interventions
DEVICEComparison 1: New Snoring Application
Measurements obtained from the snoring application under development
DEVICEComparison 2: Commercially Available Snoring Application
Measurements from a commercially available snoring application
DEVICEComparison 3: Polysomnography
Measures taken from home or in laboratory polysomnography
Sponsors
Windsor Sleep Disorders Clinic
Study design
Observational model
COHORT
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Referred for a diagnostic sleep study
Exclusion criteria
* Under the age of 18
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Snoring | 1 Night recording with all 3 devices | Objective Measurements of snoring intensity (decibel) |
| Apneas | 1 Night recording with all 3 devices | Frequency of Apneas (events per hour) |
Outcome results
None listed