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MyOSA : Management and Treatment of Patients With Obstructive Sleep Apnea Syndrome(OSAS) Through a Telemedicine System (MyOSA)

Primary Purpose

Sleep Apnea Syndrome

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
CPAP + Standard care
CPAP + Telemedicine
Sponsored by
Sociedad Española de Neumología y Cirugía Torácica
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Experimental

Arm Label

Standard care

Telemedicine

Arm Description

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.

Outcomes

Primary Outcome Measures

CPAP compliance
Number of hours of use per day of CPAP according to the internal clock of the CPAP device

Secondary Outcome Measures

CPAP adherence
Numbers of night with more than 4 hours of use
Patients' perceived ease of use of the telemedicine system
Patients in the telemedicine group will be asked to grade the perceived ease of use of the telemedicine platform using a questionnaire
Patients' perceived useful of the telemedicine system
Patients in the telemedicine group will be asked to grade the perceived useful of the telemedicine platform using a questionnaire
Patients' follow-up satisfaction
Patients of both group will be asked to grade their satisfaction with the follow up care provided by the sleep unit using a questionnaire.
Change from baseline in quality of life at 6 months
EuroQOL health questionnaire will be used.
Change from baseline in daytime sleepiness at 6 months
Epworth sleepiness scale will be used.
Abandons at 6 months
Number of patients lost at follow up at 6 months of CPAP therapy.
Cost effectiveness at 6 months
Costs in each group (telemedicine cost, CPAP carrying charge, number of visits and calls) will be compared.
Changes in treatment side effects
Change in blood pressure at 6 months
Change in body mass index (in kg/m^2) at 6 months
Change from baseline in Visual analogue scale for quality of life at 6 months
Visual analogue scale for quality of life will be used
Change in weight (in kg) at 6 months

Full Information

First Posted
April 3, 2017
Last Updated
April 5, 2019
Sponsor
Sociedad Española de Neumología y Cirugía Torácica
Collaborators
Fundació Eurecat
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1. Study Identification

Unique Protocol Identification Number
NCT03116958
Brief Title
MyOSA : Management and Treatment of Patients With Obstructive Sleep Apnea Syndrome(OSAS) Through a Telemedicine System
Acronym
MyOSA
Official Title
MyOSA : Management and Treatment of Patients With Obstructive Sleep Apnea Syndrome(OSAS) Through a Telemedicine System
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
November 2016 (undefined)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
December 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sociedad Española de Neumología y Cirugía Torácica
Collaborators
Fundació Eurecat

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to improve CPAP treatment compliance of Obstructive Sleep Apnea Syndrome using an integrated telemedicine platform (MyOSA system)
Detailed Description
Obstructive Sleep Apnea (OSA) is defined by the presence of repetitive episodes of upper airways collapse during sleep, leading to nocturnal hypoxemia, sleep fragmentation and daytime sleepiness. When untreated, OSA is a risk factor for arterial hypertension , cardiovascular and cerebrovascular diseases, road accidents and a worse quality of life. The application of a continuous positive airways pressure (CPAP) represents the first line therapy in patients with moderate to severe OSA. CPAP treatment improves daytime sleepiness and oxygen saturation, reduces cardiovascular risk, ameliorates neurobehavioral performance, improves quality of life and reduces road accidents. Despite its demonstrated efficacy, CPAP effectiveness is significantly limited by poor adherence. A closer follow up could improve CPAP adherence but it would take up more work and additional costs for sleep units. So, on that account, the investigators propose a study to evaluate the effect of adding a telemedicine approach to traditional follow up on CPAP treatment compliance, patients' satisfaction and follow-up costs. Telemedicine will be provided by an integrated platform composed by a web site (https://www.myosa.net/menu/login.aspx) and a smartphone application. Methods: Design: Prospective randomised clinical study. Follow up: 6 months. Participants: 60 patients diagnosed as OSA at St. Maria's Hospital (Sleep Unit) and requiring CPAP treatment. Randomization: Patients will be randomized into two groups differing in CPAP treatment management (standard care vs. telemedicine). Patients of both groups will be visited in Sleep Unit at 3st and 6th month after starting CPAP treatment. The CPAP machine of both groups will be provided with a modem sending daily information about CPAP treatment compliance and adherence to MyOSA web site (this kind of information will only be actively used during the follow-up in the telemedicine group). Intervention: Group 1- Telemedicine Patients will be fitted with a mask , given a CPAP, and instructed on how to use the device. An intelligent software specifically developed for this project will be integrated in the web site. Using patients' baseline data (sociodemographic characteristics, presence of comorbidities, quality of life, sleepiness, pharmacologic treatment, toxic habits), the software will be capable to provide an initial prediction of the expected CPAP compliance at 6 months. Then, the real data about patients' treatment compliance sent on daily base by the CPAP machine will train the software improving the level of confidence of the prediction. Based on the prediction of compliance at six months, the software will provide specific and personalized interventions to modify or maintain this prediction. Interventions will be administered to the patients through a smartphone application connected to the web site and specifically developed for this study (MyOSA-App). Using the mobile-app patients will receive information about their own CPAP compliance and advice on how to improve compliance. 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. Group 2- Standard 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…).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea Syndrome
Keywords
CPAP compliance, Telemedicine integrated platform, Standard management, Cost-effectiveness

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard care
Arm Type
Active Comparator
Arm Description
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…).
Arm Title
Telemedicine
Arm Type
Experimental
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
CPAP + Standard care
Intervention Description
CPAP device + Standard management at Sleep Unit. According to Spanish Respiratory Society guidelines during 6 months
Intervention Type
Device
Intervention Name(s)
CPAP + Telemedicine
Intervention Description
CPAP+ telemedicine approach. Patients followed up at Sleep Unit according to Spanish Respiratory Society guidelines during 6 months.
Primary Outcome Measure Information:
Title
CPAP compliance
Description
Number of hours of use per day of CPAP according to the internal clock of the CPAP device
Time Frame
6 months
Secondary Outcome Measure Information:
Title
CPAP adherence
Description
Numbers of night with more than 4 hours of use
Time Frame
6 months
Title
Patients' perceived ease of use of the telemedicine system
Description
Patients in the telemedicine group will be asked to grade the perceived ease of use of the telemedicine platform using a questionnaire
Time Frame
6 months
Title
Patients' perceived useful of the telemedicine system
Description
Patients in the telemedicine group will be asked to grade the perceived useful of the telemedicine platform using a questionnaire
Time Frame
6 months
Title
Patients' follow-up satisfaction
Description
Patients of both group will be asked to grade their satisfaction with the follow up care provided by the sleep unit using a questionnaire.
Time Frame
6 months
Title
Change from baseline in quality of life at 6 months
Description
EuroQOL health questionnaire will be used.
Time Frame
at baseline and 6 months
Title
Change from baseline in daytime sleepiness at 6 months
Description
Epworth sleepiness scale will be used.
Time Frame
at baseline and 6 months
Title
Abandons at 6 months
Description
Number of patients lost at follow up at 6 months of CPAP therapy.
Time Frame
6 months
Title
Cost effectiveness at 6 months
Description
Costs in each group (telemedicine cost, CPAP carrying charge, number of visits and calls) will be compared.
Time Frame
6 months
Title
Changes in treatment side effects
Time Frame
6 months
Title
Change in blood pressure at 6 months
Time Frame
at baseline and 6 months
Title
Change in body mass index (in kg/m^2) at 6 months
Time Frame
at baseline and 6 months
Title
Change from baseline in Visual analogue scale for quality of life at 6 months
Description
Visual analogue scale for quality of life will be used
Time Frame
at baseline and 6 months
Title
Change in weight (in kg) at 6 months
Time Frame
at baseline and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ferran Barbe, MD
Organizational Affiliation
Hospital Arnau de Vilanova. IRB Lleida. CIBERes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Arnau de Vilanova
City
Lleida
ZIP/Postal Code
25198
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34661550
Citation
Turino C, Benitez ID, Rafael-Palou X, Mayoral A, Lopera A, Pascual L, Vaca R, Cortijo A, Moncusi-Moix A, Dalmases M, Vargiu E, Blanco J, Barbe F, de Batlle J. Management and Treatment of Patients With Obstructive Sleep Apnea Using an Intelligent Monitoring System Based on Machine Learning Aiming to Improve Continuous Positive Airway Pressure Treatment Compliance: Randomized Controlled Trial. J Med Internet Res. 2021 Oct 18;23(10):e24072. doi: 10.2196/24072.
Results Reference
derived
PubMed Identifier
30227856
Citation
Rafael-Palou X, Turino C, Steblin A, Sanchez-de-la-Torre M, Barbe F, Vargiu E. Comparative analysis of predictive methods for early assessment of compliance with continuous positive airway pressure therapy. BMC Med Inform Decis Mak. 2018 Sep 18;18(1):81. doi: 10.1186/s12911-018-0657-z.
Results Reference
derived

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MyOSA : Management and Treatment of Patients With Obstructive Sleep Apnea Syndrome(OSAS) Through a Telemedicine System

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