Skip to main content
OpenTrials
Completed

NCT Number: NCT02055027

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

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

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre Hospitalier Universitaire (CHU) Sart-Tilman

Liège, Liege, 4000, Belgium

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Comparison between groups

Other

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

Primary outcomes

  1. Number of hours of CPAP use by night

    Time frame: Baseline

    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)

Secondary outcomes

  1. Lickert's scale to assess criteria of non-adherence

    Time frame: Baseline

    Evaluation of 72 criteria by a Lickert's scale in order to assess characteristics associated with non-adherence to CPAP therapy

Sponsors and collaborators

Lead sponsor

Astes

Other

Registry information

Official study title

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

Important dates

Study start
2008
Primary completion
2008
Study completion
2008
First posted
Feb 4, 2014
Registry last updated
Feb 4, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.