Validation of a Snoring App Against Commercially Available Applications and PSG

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWindsor Sleep Disorders Clinic

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Referred for a diagnostic sleep study

Disqualifiers

Under the age of 18

Trial population

Patients referred for a diagnostic sleep study at the Windsor Sleep Disorders Clinic

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

  • 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

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Sleep Laboratory Patients3 interventions

Trial outcomes

Primary outcomes

1

Snoring

Objective Measurements of snoring intensity (decibel)

Time frame
1 Night recording with all 3 devices
2

Apneas

Frequency of Apneas (events per hour)

Time frame
1 Night recording with all 3 devices
3

Snoring

Frequency of snoring (counts)

Time frame
1 Night recording with all 3 devices

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: