Adherence to Continuous Positive Airway Pressure Among Obstructive Sleep Apnoea Patients.
1 other identifier
observational
90
1 country
1
Brief Summary
Prospective study designed to identify factors that would predict patient adherence to CPAP (Continuous Positive Airway Pressure) therapy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2008
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2008
CompletedFirst Submitted
Initial submission to the registry
February 3, 2014
CompletedFirst Posted
Study publicly available on registry
February 4, 2014
CompletedFebruary 4, 2014
February 1, 2014
29 days
February 3, 2014
February 3, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of hours of CPAP use by night
Analyse of the data recorded by the CPAP microchip in order to assess the adherent or non-adherent status to the patient (adherent: CPAP use \> 4 hours per night, non-adherent: less than 4 hours)
Baseline
Secondary Outcomes (1)
Lickert's scale to assess criteria of non-adherence
Baseline
Study Arms (2)
Adherent Patients
Comparison between groups
Non-adherent patients
Comparison between groups
Interventions
Comparison between the two groups (adherent and non-adherent patients) in order to discover criteria of non-adherence
Eligibility Criteria
Sleep Study Center
You may qualify if:
- Adults (\> 18 patients)
- All patients under CPAP (Continuous Positive Airway Pressure) therapy coming for annual visit in the Sart-Tilman Sleep Study Center
You may not qualify if:
- Patient refusal
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Asteslead
Study Sites (1)
Centre Hospitalier Universitaire (CHU) Sart-Tilman
Liège, Liege, 4000, Belgium
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Eric Deflandre, MD, FCCP
Astes
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Eric DEFLANDRE, MD, FCCP
Study Record Dates
First Submitted
February 3, 2014
First Posted
February 4, 2014
Study Start
February 1, 2008
Primary Completion
March 1, 2008
Study Completion
April 1, 2008
Last Updated
February 4, 2014
Record last verified: 2014-02