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Chronic Care Management With Wearable Devices in Patients Prescribed Positive Airway Pressure Therapy (mPAP) Trial — mPAP  

Obstructive Sleep Apnea Clinical Trial

Official title:
Augmenting Obstructive Sleep Apnea Chronic Care Management With Consumer Wearable Devices in Patients Prescribed Positive Airway Pressure Therapy

Clinical Trial Summary

The goal of this clinical trial in adults with obstructive sleep apnea prescribed positive airway pressure therapy is to test the effects of a new patient-facing consumer wearable-based program (that involves provision of a consumer wearable that measures oxygen levels during sleep plus customized weekly reports to participants). The main question is to learn whether participants' use of positive airway pressure therapy will differ between the participants who receive the new program immediately versus delayed. Participants assigned to the delayed program will receive usual care while waiting for the program to begin.

Clinical Trial Description

After being informed about the study and potential risks, all patients giving written informed consent will undergo a screening to determine eligibility for study entry. Patients who meet the eligibility requirements will be randomized to immediate versus waitlist control in a 1:1 ratio. Our project is at the forefront of consumer wearable research, leveraging the recent capabilities of consumer wearables to provide pulse oximetry data during sleep, to uncover new ways to promote PAP usage among patients with obstructive sleep apnea. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06039865
Study type Interventional
Source VA Greater Los Angeles Healthcare System
Contact Constance H. Fung, MD, MSHS
Phone 818 891-7711
Email Constance.Fung@va.gov
Status Recruiting
Phase N/A
Start date October 20, 2023
Completion date September 30, 2024
View Details
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