MonitAir Remote Patient Monitoring Versus Standard of Care for CPAP Adherence in Obstructive Sleep Apnea

Completed · Not applicable

Conditions studied: Obstructive Sleep Apnea (OSA)

In brief

This study tested whether using the MonitAir remote patient monitoring (RPM) platform could improve adherence to continuous positive airway pressure (CPAP) therapy for patients with obstructive sleep apnea. Patients starting CPAP treatment with BetterNight were randomized to receive either standard coaching (control group) or enhanced monitoring with the MonitAir platform (intervention group). The study measured CPAP adherence at 30, 60, and 90 days, as well as patient satisfaction and other clinical outcomes.

Key facts

Study ID: NCT07182617
Run by: MonitAir
People needed: 200
Starts: 2024-02-05
Expected to finish: 2025-04-01
Last updated by the study team: 2025-09-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Adults ≥18 years old
Access to a smartphone (iOS or Android)
Ability to engage in two-way text communication and audiovisual conferencing
Home sleep test (HST) or polysomnogram (PSG) performed ≤90 days before randomization
Apnea-Hypopnea Index (AHI) ≥5 (using 3% desaturation criteria)
Prescribed and willing to initiate CPAP or APAP therapy
Receiving a ResMed, Philips, or React CPAP device with a cellular modem
CPAP data available to MonitAir and BetterNight

You may not qualify if…

Department of Transportation (DOT) drivers
Central sleep apnea or Cheyne-Stokes respirations (CSA/CSR) ≥10% of diagnostic study
Central or mixed apneas ≥25% of AHI
Use of BiPAP, BiPAP ST, ASV, AVAPS, or any other non-invasive ventilation modality
Inability or unwillingness to participate in study activities or meet requirements

Where it is running

Remote — Miami, Florida, United States

Full record on ClinicalTrials.gov

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