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Clinical Trial Summary

The study will examine the usability of a breathing platform in the home environment. It will be a randomized, open-label crossover study of 10 participants who will complete the CBT and breathing components in their home, prior to sleeping. Usability will be measured by scores assigned by participants. Qualitative feedback and compliance information will also be collected.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04776122
Study type Interventional
Source ResMed
Contact
Status Completed
Phase N/A
Start date June 1, 2018
Completion date July 30, 2018

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