MyOSA : Management and Treatment of Patients With Obstructive Sleep Apnea Syndrome(OSAS) Through a Telemedicine System (MyOSA)
Sleep Apnea Syndrome
About this trial
This is an interventional health services research trial for Sleep Apnea Syndrome focused on measuring CPAP compliance, Telemedicine integrated platform, Standard management, Cost-effectiveness
Eligibility Criteria
Inclusion Criteria:
- Men and Women over 18 years old
- Diagnosed as OSA and requiring CPAP treatment
- Good knowledge of the use of a smartphone
- Written informed consent form signed
Exclusion Criteria:
- Patients with impaired lung function (overlap syndrome, obesity hypoventilation syndrome, and restrictive disorders)
- Severe heart failure
- Severe chronic pathology associated
- Psychiatric disorder
- Periodic leg movements
- Pregnancy
- Other dyssomnias or parasomnias
- Patients already treated with CPAP
Sites / Locations
- Hospital Arnau de Vilanova
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Standard care
Telemedicine
Patients diagnosed as OSA, treated with CPAP and followed up in sleep unit as per usual care. Patients will be fitted with a mask and given a CPAP and instructed on how to use the device. Each CPAP machine will be provided with a modem sending daily compliance and adherence information to MyOSA web site but no intervention based on these data is planned in this group. All patients will be visited at 1,3 and 6 months at sleep unit. Patients will be checked about progress and adherence to therapy and any problems with their machine. Information will be downloaded from their machines (CPAP adherence, applied CPAP pressure, mask leak, and residual respiratory events…).
Patients diagnosed as OSA and treated with CPAP, followed up in sleep unit, adding a telemedicine integrated system. Patients will be fitted with a mask , given a CPAP, and instructed on how to use the device. Using patients' baseline and initial follow-up data a software will provide a prediction of CPAP compliance at 6 months, and propose personalized interventions to increase compliance (smartphone app). All patients will be visited at 3 and 6 months at sleep unit. Patients will be checked about progress and adherence to therapy and any problems with their machine.