Snore Positive Airway Pressure Trial

Not Applicable

Completed

• Conditions: Non-Apnoeic Snorers

• Registration Number: NCT03201055
• Lead Sponsor: ResMed

Brief Summary

This study will aim to assess the acceptance of the Snore PAP system as a treatment concept for snore. The study will subjectively assess participant and bed partner acceptability and usability of the Snore PAP system and objectively assess participant compliance with the Snore PAP system.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-06-22
• Study First Submitted QC: 2017-06-26
• Study First Posted: 2017-06-28
• Study Start: 2017-10-02
• Primary Completion: 2018-07-31
• Study Completion: 2019-07-31
• Status Verified: 2021-02
• Last Update Submitted: 2021-02-17
• Last Update Posted: 2021-02-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Subjectively assess the participant and bed partner acceptability and usability of Snore PAP system	28 Nights	Subjective assessment will be assessed using the Likert scale using a 0-10 scale. With 0 being very negative and 10 being very positive.

Secondary Outcome Measures

Name	Time	Method
Objectively assess participant compliance with the Snore PAP system	28 Nights	Hours used per night
Subjectively assess the performance of the Snore PAP system in relieving: self-reported and bed partner reported snore in non-apnoeic participants.	28 Nights	Subjective assessment will be assessed using the Likert scale using a 0-10 scale. With 0 being very negative and 10 being very positive.

Trial Locations

Locations (1)

EdenSleep; 🇳🇿 New Plymouth, New Zealand