NCT07097597

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).

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Sep 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 16, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

July 31, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2026

Completed
Last Updated

July 31, 2025

Status Verified

July 1, 2025

Enrollment Period

5 months

First QC Date

July 16, 2025

Last Update Submit

July 24, 2025

Conditions

SnoringObstructive Sleep Apnea (OSA)

Outcome Measures

Primary Outcomes (3)

  • Snoring

    Objective Measurements of snoring intensity (decibel)

    1 Night recording with all 3 devices

  • Apneas

    Frequency of Apneas (events per hour)

    1 Night recording with all 3 devices

  • Snoring

    Frequency of snoring (counts)

    1 Night recording with all 3 devices

Study Arms (1)

Sleep Laboratory Patients

Device: Comparison 1: New Snoring ApplicationDevice: Comparison 2: Commercially Available Snoring ApplicationDevice: Comparison 3: Polysomnography

Interventions

Comparison 1: New Snoring ApplicationDEVICE

Measurements obtained from the snoring application under development

Sleep Laboratory Patients
Comparison 2: Commercially Available Snoring ApplicationDEVICE

Measurements from a commercially available snoring application

Sleep Laboratory Patients
Comparison 3: PolysomnographyDEVICE

Measures taken from home or in laboratory polysomnography

Sleep Laboratory Patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • Referred for a diagnostic sleep study

You may not qualify if:

  • Under the age of 18

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

SnoringSleep Apnea, Obstructive

Condition Hierarchy (Ancestors)

Respiratory SoundsSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and SymptomsSleep Apnea SyndromesApneaRespiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System Diseases

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 16, 2025

First Posted

July 31, 2025

Study Start

September 1, 2025

Primary Completion

January 31, 2026

Study Completion

January 31, 2026

Last Updated

July 31, 2025

Record last verified: 2025-07