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Validation of Software for Assessment of Sleep Apnea From Data Acquired by a Wearable Smartwatch

Sleep Apnea Clinical Trial

Official title:
Fitbit Sleep Apnea Alert Software Validation Study

Clinical Trial Summary

This clinical validation study aims to evaluate the utility of Fitbit's Sleep Apnea Alert software for minimally invasive monitoring of sleep apnea events to alert users of their risk of sleep apnea. The Sleep Apnea Alert software analyses data from a Fitbit commercially available wrist photoplethysmogram (PPG) device. The Sleep Apnea Alert software is an investigational software as medical device (SaMD) and is designed to retrospectively process data and flag users who have physiological signals consistent with an apnea-hypopnea index (AHI) of 15 or greater. This clinical validation study will be used to validate Fitbit's PPG-based sleep apnea algorithm. The outputs of the Fitbit Sleep Apnea Alert software will not be available to study participants, as the scope of this study is to gather validation data only and does not include testing product usability components.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03775291
Study type Observational
Source Fitbit Inc
Contact
Status Active, not recruiting
Phase
Start date November 9, 2018
Completion date April 30, 2023
View Details
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