The effectiveness of remote monitoring in improving CPAP compliance: a randomised, controlled study.

Completed

• Conditions: slaapgeneeskunde/OSAS; obstructive sleep apnea; OSAS; 10038716

• Registration Number: NL-OMON41977
• Lead Sponsor: Amphia Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 250

Inclusion Criteria

- newly diagnosed OSAS patient
- apnea hypopnea index > 29/hour
- CPAP therapy
- Age between 18-75 years

Exclusion Criteria

- anxiety disorder
- mental disorder/retardation
- significant central sleep apnea component
- expected other changes in physical well being cause of comorbidity/other diseases and expected weight loss or gain such as pregnancy, bariatric surgery.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>mean hours/night CPAP use after 10 weeks, compared between the two groups.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>a. Number of patients who stop their therapie after 10 weeks and after 1 year<br /><br>b. Increased efficiency of treatment, regarding check-up's and hospital visits<br /><br>c. CPAP related complaints/symptoms</p><br>