| Methods |
Randomised parallel‐group trial |
| Participants |
n = 166. Inclusion criteria: 1) >18 years old, 2) moderate to severe OSA (apnoea hypopnoea index (AHI) ≥15 events/hour) on polysomnogram (PSG), 3) Followed by non‐sleep providers for OSA (mainly primary care providers), 4) New PAP set up < 1 month. 5) Sub‐optimal PAP adherence by objective PAP adherence data (<70 % usage and <4 hours of average PAP usage) |
| Interventions |
Sleep Apnea Management (SAM) Clinic vs. Usual Care with the non‐sleep provider |
| Outcomes |
Hours of PAP usage (>4 hours), % days of PAP use in, ESS, PHQ‐9, PROMIS Global Health, PROMIS Fatigue, PROMIS Sleep Related Impairment, PAP Barrier questionnaire |
| Notes |
Reason for "Awaiting Classification" Status: unable to confirm review inclusion criteria at this time, Results data for this study not currently available |
