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Impacts of a Continuing Education Activity Targeted at COPD Case Managers

Comparing the Impacts of Two Versions of a Continuing Education Activity Targeted at COPD Case Managers on Educational Outcomes

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02870998
Enrollment
300
Registered
2016-08-18
Start date
2016-06-30
Completion date
2019-11-30
Last updated
2019-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Diseases, Obstructive

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.

Interventions

1-day continuing education activity consisting of a lecture on patient education.

OTHERPassive learning

1-day continuing education activity consisting of a brief lecture on patient education and workshops.

Sponsors

Laval University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

for attendees: * Attending the continuing education activity * Providing patient education to individuals with COPD in professional setting.

Exclusion criteria

for attendees: * None Inclusion criteria for COPD patients: * Doctor-diagnosed COPD.

Design outcomes

Primary

MeasureTime frameDescription
Performance2-month post-interventionWe 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

MeasureTime frameDescription
SatisfactionImmediately post-interventionWe will measured the extent to which attendees' expectations about the continuing education activity are met, using a self-administered questionnaire.
LearningPrior to and 1-month post-interventionWe will measured declarative and procedural knowledge about patient education in attendees, using a validated self-administered questionnaire.
CompetencePrior and immediately post-interventionWe will measure attendees' self-reported competences in achieving learning activity objectives, using a self-administered questionnaire.
Patient health outcomes4-month and 10-month post-interventionWe will measured COPD patients' health-related quality of life, self-management skills, and health utilization, using validated interviewer-administered questionnaires.

Countries

Canada

Contacts

Primary ContactMyriam Gagne, MSc
myriam.gagne@criucpq.ulaval.ca1-418-656-8711

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026