NCT03792880.
Methods | Randomised parallel‐group trial |
Participants | n = 60 Inclusion criteria: 1) Patients with a recent diagnostic of OSAHS with AHI ≥ 30 and indication of CPAP, 2) age,≥ 18 years, 3) Few symptoms,without hyper somnolence (Epworth sleepiness scale ≤ 10) 4) Absence of clinic suspect or confirmation of other sleep pathology. 5)With interest in the use of new technologies |
Interventions | telemedicine vs. standard care |
Outcomes | % patients with a CPAP compliance ≥4 hours per day, CPAP compliance, dropouts, side effects, ESS, change in snoring, frequency of refreshing sleep, air leaks and residual AHI, EuroQoL, circadian rhythm parameters, cost‐effectiveness |
Notes | Reason for "Awaiting Classification" Status: unable to confirm review inclusion criteria at this time, Results data for this study not currently available |