The primary aim of this study is to validate the performance of Sleepiz One+ for the measurement of vital physiological parameters in adult population, against a laboratory-based polysomnography. Additionally, the investigators will evaluate Sleepiz One+ ability to identify patients with a high risk of suffering from a sleep-related breathing disorder based on apnea-hypopnea index estimation. Participants will undergo measurement with Sleepiz One+ and a polysomnography device while resting in bed for 20 min as well as during sleep for the duration of the following night.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
64
Simultaneous sleep study with polysomnography and Sleepiz One+
Simultaneous sleep study with polysomnography and Sleepiz One+
Klinik Lengg AG
Zurich, Switzerland
Respiration rate measurement accuracy agreement
Time frame: 60 seconds
Binary classification of sleep apnea severity based on the AHI > 15 of Sleepiz One+ compared to results of Domino software and data manually scored by sleep technician
Time frame: 1 Night
Instantaneous respiration rate agreement between Sleepiz One+ and nasal cannula
Time frame: 60 seconds
Average respiration rate agreement between Sleepiz One+ and thoracic respiratory effort belt
Time frame: 1 Night
Average respiration rate agreement between Sleepiz One+ and nasal cannula
Time frame: 1 Night
Sleep/wake classification agreement between Sleepiz One+ compared to polysomnography (PSG) data manually scored by sleep technician
Time frame: 60 seconds
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