Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Mayo Clinic
With
Arizona State University
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
In both trials of Aim 2, twenty adults (≥18 years) per trial will be recruited who are newly diagnosed with OSA and speak English.
In both trials, we will purposely recruit samples balanced by biological sex and OSA severity (apnea hypopnea index: 5-14 vs. ≥ 15).
* Are diagnosed with OSA based on clinical diagnostic testing via laboratory or home-based sleep study;
* Own and have the functional and cognitive ability to use an Apple (iOS9 or higher) or Android (4.2 or higher) smartphone with minimal to no assistance;
* Are prescribed continuous or auto-titrated CPAP;
* Agree to using a smartphone application and wearable wrist sensor; and
* Speak and read English.
You may not be if
Unwilling to complete study measures and engage with SleepWell24;
Refuse to not use the Fitbit application during the study trial;
Have any conditions that would impede full participation (e.g., communication or cognitive impairments that limit ability to read and/or follow directions, other acute or severe health, cognitive, or psychological conditions);
Currently participating in other lifestyle programs (e.g. active, formal weight loss program or research study; smoking cessation program, etc.);
Decide to use a different PAP device than ResMed Airsense 10;
Prescribed high-dose benzodiazepines (equivalent to \> 1 mg lorazapam/night);
Daily opioid medication use at night;'
Unwilling to discontinue use of any current wearable sensor for the duration of the trial;
Previous documented history of treatment/referral for claustrophobia;
Previous CPAP use;
Currently engaging in shiftwork defined as night shift or rotating day and night shifts; and
Currently pregnant, trying to conceive, or breastfeeding.
Clareo Health | App-Based Optimization of Long-Term CPAP Adherence and Quality of Life
