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Impacts of a Continuing Education Activity Targeted at COPD Case Managers

Primary Purpose

Lung Diseases, Obstructive

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Active learning
Passive learning
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Lung Diseases, Obstructive

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Institut universitaire de cardiologie et de pneumologie de QuébecRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Active learning

Passive learning

Arm Description

Educational strategies will be used to foster active learning.

Traditional educational strategies (lecture) will be used.

Outcomes

Primary Outcome Measures

Performance
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

Satisfaction
We will measured the extent to which attendees' expectations about the continuing education activity are met, using a self-administered questionnaire.
Learning
We will measured declarative and procedural knowledge about patient education in attendees, using a validated self-administered questionnaire.
Competence
We will measure attendees' self-reported competences in achieving learning activity objectives, using a self-administered questionnaire.
Patient health outcomes
We will measured COPD patients' health-related quality of life, self-management skills, and health utilization, using validated interviewer-administered questionnaires.

Full Information

First Posted
March 15, 2016
Last Updated
February 25, 2019
Sponsor
Laval University
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1. Study Identification

Unique Protocol Identification Number
NCT02870998
Brief Title
Impacts of a Continuing Education Activity Targeted at COPD Case Managers
Official Title
Comparing the Impacts of Two Versions of a Continuing Education Activity Targeted at COPD Case Managers on Educational Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 2016 (undefined)
Primary Completion Date
November 2019 (Anticipated)
Study Completion Date
November 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laval University

4. Oversight

Data Monitoring Committee
No

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Diseases, Obstructive

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active learning
Arm Type
Experimental
Arm Description
Educational strategies will be used to foster active learning.
Arm Title
Passive learning
Arm Type
Active Comparator
Arm Description
Traditional educational strategies (lecture) will be used.
Intervention Type
Other
Intervention Name(s)
Active learning
Intervention Description
1-day continuing education activity consisting of a lecture on patient education.
Intervention Type
Other
Intervention Name(s)
Passive learning
Intervention Description
1-day continuing education activity consisting of a brief lecture on patient education and workshops.
Primary Outcome Measure Information:
Title
Performance
Description
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.
Time Frame
2-month post-intervention
Secondary Outcome Measure Information:
Title
Satisfaction
Description
We will measured the extent to which attendees' expectations about the continuing education activity are met, using a self-administered questionnaire.
Time Frame
Immediately post-intervention
Title
Learning
Description
We will measured declarative and procedural knowledge about patient education in attendees, using a validated self-administered questionnaire.
Time Frame
Prior to and 1-month post-intervention
Title
Competence
Description
We will measure attendees' self-reported competences in achieving learning activity objectives, using a self-administered questionnaire.
Time Frame
Prior and immediately post-intervention
Title
Patient health outcomes
Description
We will measured COPD patients' health-related quality of life, self-management skills, and health utilization, using validated interviewer-administered questionnaires.
Time Frame
4-month and 10-month post-intervention

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Myriam Gagne, MSc
Phone
1-418-656-8711
Ext
2714
Email
myriam.gagne@criucpq.ulaval.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louis-Philippe Boulet, MD
Organizational Affiliation
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut universitaire de cardiologie et de pneumologie de Québec
City
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Myriam Gagné, MSc
Phone
4186568711
Ext
2714
Email
myriam.gagne@criucpq.ulaval.ca

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The datasets during and/or analysed during the current study will be available from the principal investigator on reasonable request.
Citations:
PubMed Identifier
31502238
Citation
Gagne M, Lauzier S, Babineau-Therrien J, Hamel C, Penney SE, Bourbeau J, Moisan J, Boulet LP. COPD-Specific Self-Management Support Provided by Trained Educators in Everyday Practice is Associated with Improved Quality of Life, Health-Directed Behaviors, and Skill and Technique Acquisition: A Convergent Embedded Mixed-Methods Study. Patient. 2020 Feb;13(1):103-119. doi: 10.1007/s40271-019-00386-7.
Results Reference
derived
PubMed Identifier
29914484
Citation
Gagne M, Moisan J, Lauzier S, Hamel C, Cote P, Bourbeau J, Boulet LP. Comparative impact of two continuing education activities targeted at COPD educators on educational outcomes: protocol for a non-randomized controlled study using mixed methods. BMC Health Serv Res. 2018 Jun 18;18(1):460. doi: 10.1186/s12913-018-3284-6.
Results Reference
derived

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Impacts of a Continuing Education Activity Targeted at COPD Case Managers

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