Adherence to Continuous Positive Airway Pressure Among Obstructive Sleep Apnoea Patients.

Sleep Apnea, Obstructive Clinical Trial

Official title:

Adherence to Continuous Positive Airway Pressure Among Obstructive Sleep Apnoea Patients. An Anaesthetic Algorithmic Approach to Prevent Postoperative Complications.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02055027
• Other study ID #: ASTES-NCPAP
• Status: Completed
• Phase: N/A
• First received: February 3, 2014
• Last updated: February 3, 2014
• Start date: February 2008
• Est. completion date: April 2008

Study information

• Verified date: February 2014
• Source: Astes
• Contact: n/a
• Is FDA regulated: No
• Health authority: Belgium: Ethics Committee
• Study type: Observational

Clinical Trial Summary

Prospective study designed to identify factors that would predict patient adherence to CPAP (Continuous Positive Airway Pressure) therapy.

Description:

Prospective study designed to identify factors that would predict patient adherence to CPAP therapy.

Comparison between data recorded among patients and the data of the CPAP microchip.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 90
• Est. completion date: April 2008
• Est. primary completion date: March 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adults (> 18 patients)

• All patients under CPAP (Continuous Positive Airway Pressure) therapy coming for annual visit in the Sart-Tilman Sleep Study Center

Exclusion Criteria:

• Patient refusal

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Apnea
• Postoperative Complications
• Sleep Apnea Syndromes
• Sleep Apnea, Obstructive

Intervention

Other:
• Comparison between groups
Comparison between the two groups (adherent and non-adherent patients) in order to discover criteria of non-adherence

Locations

Country	Name	City	State
Belgium	Centre Hospitalier Universitaire (CHU) Sart-Tilman	Liege

Sponsors (1)

Lead Sponsor	Collaborator
Astes

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	Yes
Secondary	Lickert's scale to assess criteria of non-adherence	Evaluation of 72 criteria by a Lickert's scale in order to assess characteristics associated with non-adherence to CPAP therapy	Baseline	Yes