Impacts of a Continuing Education Activity Targeted at COPD Case Managers

Sponsor
Laval University (Other)
Overall Status
Unknown status
CT.gov ID
NCT02870998
Collaborator
(none)
300
1
2
41
7.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Active learning
  • Other: Passive learning
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Comparing the Impacts of Two Versions of a Continuing Education Activity Targeted at COPD Case Managers on Educational Outcomes
Study Start Date :
Jun 1, 2016
Anticipated Primary Completion Date :
Nov 1, 2019
Anticipated Study Completion Date :
Nov 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Active learning

Educational strategies will be used to foster active learning.

Other: Active learning
1-day continuing education activity consisting of a lecture on patient education.

Active Comparator: Passive learning

Traditional educational strategies (lecture) will be used.

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

Outcome Measures

Primary Outcome Measures

  1. Performance [2-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

  1. Satisfaction [Immediately post-intervention]

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

  2. Learning [Prior to and 1-month post-intervention]

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

  3. Competence [Prior and immediately post-intervention]

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

  4. Patient health outcomes [4-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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts 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.
Exclusion criteria for attendees:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institut universitaire de cardiologie et de pneumologie de Québec Quebec Canada G1V 4G5

Sponsors and Collaborators

  • Laval University

Investigators

  • Principal Investigator: Louis-Philippe Boulet, MD, Institut universitaire de cardiologie et de pneumologie de Québec

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Louis-Philippe Boulet, MD, Laval University
ClinicalTrials.gov Identifier:
NCT02870998
Other Study ID Numbers:
  • MP-10-2016-2591
First Posted:
Aug 18, 2016
Last Update Posted:
Feb 27, 2019
Last Verified:
Feb 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 27, 2019