Snore Positive Airway Pressure Trial
Not Applicable
Completed
- Conditions
- Non-Apnoeic Snorers
- Interventions
- Device: Snore PAP System
- 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
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
- Arm && Interventions
Group Intervention Description Non Apnoeic Snorers Snore PAP System Patient's use the Snore Positive airway pressure device for 28 nights.
- 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