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Impacts of a Continuing Education Activity Targeted at COPD Case Managers

Not Applicable
Conditions
Lung Diseases, Obstructive
Interventions
Other: Active learning
Other: Passive learning
Registration Number
NCT02870998
Lead Sponsor
Laval University
Brief Summary

This study aims to compare the impacts of two versions of a continuing education activity targeted at COPD case managers on educational outcomes: 1) participation; 2) satisfaction; 3) learning; 4) competence; 5) performance; 6) patient health outcomes.

Detailed Description

This study has a quasi-experimental design. The study is based on the Expanded Outcomes Framework for Planning and Assessing Continung Medical Education by Moore (2009). One groupe of participants will attend the former version of the continuing education activity, and the other group will attend its new version.

Data will be collected at T0 (before the activity, which will be held at T1); at T2 (immediately after the activity); at T3 (1-month post-activity); at T4 (2-month post-activity); at T5 (4-month post-activity); at T6 (10-month post-activity).

Participation will be assessed at T0. Satisfaction will be assessed at T2. Learning will be assessed at T0 and T3. Competence will be assessed at T2. Performance will be assessed at T4. Patient health outcomes will be assessed at T5 and T6.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
300
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Active learningActive learningEducational strategies will be used to foster active learning.
Passive learningPassive learningTraditional educational strategies (lecture) will be used.
Primary Outcome Measures
NameTimeMethod
Performance2-month post-intervention

We will videotape patient education intervention delivered by attendees in their professional practice and will assess the quality of the delivered patient education intervention using a set a pre-defined criteria.

Secondary Outcome Measures
NameTimeMethod
SatisfactionImmediately post-intervention

We will measured the extent to which attendees' expectations about the continuing education activity are met, using a self-administered questionnaire.

CompetencePrior and immediately post-intervention

We will measure attendees' self-reported competences in achieving learning activity objectives, using a self-administered questionnaire.

Patient health outcomes4-month and 10-month post-intervention

We will measured COPD patients' health-related quality of life, self-management skills, and health utilization, using validated interviewer-administered questionnaires.

LearningPrior to and 1-month post-intervention

We will measured declarative and procedural knowledge about patient education in attendees, using a validated self-administered questionnaire.

Trial Locations

Locations (1)

Institut universitaire de cardiologie et de pneumologie de Québec

🇨🇦

Quebec, Canada

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