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NCT03151317 Clinical Trial

Effects of a Therapeutic Education Program on Treatment Adherence Among Patients Prescribed At-home CPAP or At-home NIV

Noninvasive Ventilation Clinical Trial

— APARDetp  

Official title:
Effects of a Therapeutic Education Program on Treatment Adherence Among Patients Prescribed At-home Continuous Positive Airway Pressure or At-home Non-invasive Ventilation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03151317
Other study ID # RECHMPL17_0077
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 12, 2017
Est. completion date July 30, 2017

Study information
Verified date May 2017
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective of this study is to study the effect of therapeutic education on patient adherence for at-home continuous positive airway pressure (CPAP) or at-home non-invasive ventilation. This first study will use data already present in the Association for Home Assistance and Rehabilitation (APARD) database to compare patients who received therapeutic education with a control group who did not.

Description:

The proposed study calendar refers to the beginning and completion of work on the APARD database.

Recruitment information / eligibility
Status Completed
Enrollment 1200
Est. completion date July 30, 2017
Est. primary completion date July 30, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients that have been equipped by the Association for Home Assistance and Rehabilitation (APARD) with either a continuous positive airway pressure (CPAP) device or a non-invasive ventilation (NIV) device.

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Apard Database Montpellier

Sponsors (2)
Lead Sponsor Collaborator
University Hospital, Montpellier Association pour l’Assistance et la Réhabilitation à Domicile (APARD)

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Treatment adherence Treatment adherence will be quantified as the average number of hours of device usage per night a period of 28 days (retrospective study)
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