Personal Therapy Comfort Settings Pilot Clinical Study

Status Completed

Clinical Trial Summary

350 participants will be enrolled in this study. The target population are patients newly diagnosed with OSA and starting CPAP treatment. User accessible customizable comfort settings (Response setting, expiratory pressure relief (EPR) on/off and EPR level, and Ramp) will be set to either default (control group), or personalized for that participant (active treatment group). Usage will be recorded for the first 1 month of CPAP treatment, to determine if customizing comfort settings can improve CPAP compliance

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05376137
Study type	Interventional
Source	ResMed
Contact
Status	Completed
Phase	N/A
Start date	September 15, 2022
Completion date	September 13, 2023

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