- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07121400
- Original Trial
E-learning Teaching During Anesthesia Residency
Pedagogical Impact of Different Levels of E-learning Teaching During Anesthesia Residency: a Randomized Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The participants first have a pre-test consisting of a clinical case and a script concordance test (SCT). The clinical case was designed to evaluate theoretical clinical knowledge. The clinical case scored 50 points and consisted of 4 open-ended questions (12,5 points for each question) on the management and complications of the diabetic patient in anesthesia. The SCT consisted of 15 questions on the management of the diabetic patient in anesthesia (degenerative neuropathy, ischemic cardiopathy, intubation, management of hyperglycemia, postoperative complications) and was also scored out of 50 points. The participants had 15 minutes for the clinical case and 15 minutes for the SCT.
The pre-test was conducted in a double-blind way, each participant did not know in which group they would be. Each test had a double-blind correction by two senior anesthesiologists. The participants were then randomized to either the Interactive-EL group (Int-EL group) or a Passive-EL group (Pass-EL group).
The Int-EL group had full access to a pedagogical internet platform with online documents; national experts' recommendations on the management of diabetic patients in anesthesia, slide presentation lectures on the topic by local university teachers, and, the possibility to contact a virtual mentor (anaesthesiologist of our department) by email for interactive discussion or questions about the topic.
The Pass-EL group only received by email the documents (French experts' recommendations and slide presentation lectures on the management of diabetic patients in anesthesia) and did not have access to the pedagogical internet platform. The e-learning training period was one month for both groups. The investigators then conducted, in both groups, a post-test composed of the same clinical case and the same SCT.
The time allotted for the post-test was identical to that of the pre-test, and students were not allowed to access external resources during either test.
Each test had a double-blind grading by two senior anesthesiologists.
The tests were developed by two experts in anesthesiology and medical education within our department. The participants in the Pass-EL group had the option to access the platform at the end of the study to complete the e-learning course, should they choose to do so.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All anesthesiology residents from first to fourth year in both centers (participants)
Exclusion Criteria:
- Exclusion criteria included residents missing the pre-or post-tests or refusing to participate in the training program.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Passive-E-Learning group (received by email the documents and didn't have access to the platform)
The Passive-E-Learning group only received by email the documents (French experts' recommendations and slide presentation lectures on the management of diabetic patients in anesthesia) and did not have access to the pedagogical internet platform.
|
|
|
Experimental: Interactive-E-Learning group
The interactive-E-Learning group (Int-EL group) had full access to a pedagogical internet platform with online documents; national experts' recommendations on the management of the diabetic patient in anesthesia, slides presentation lectures on the topic by local university teachers, and, the possibility to contact a virtual mentor (anaesthesiologist of our department) by email for interactive discussion or questions about the topic.
The course website was constructed using an online secured program with a unique identification form and password for each resident of the Int-EL group.
|
The Interactive-E-learning group had full access to a pedagogical internet platform with online documents; national experts' recommendations on the management of diabetic patients in anesthesia, slide presentation lectures on the topic by local university teachers, and, the possibility to contact a virtual mentor (anaesthesiologist of our department) by email for interactive discussion or questions about the topic.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of the theoretical clinical knowledge score between the two e-learning groups
Time Frame: One month after pre-test
|
The score used was the means of the paired within-subject differences (delta) of clinical knowledge scores (pre-and post-test).
The score could range from 0 to 50 points.
|
One month after pre-test
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The comparison of clinical reasoning scores between the two e-learning groups
Time Frame: one month
|
Evaluated by the paired within-subject differences (delta) SCT scores (pre-and post-test).
The score could range from 0 to 50 points.
|
one month
|
|
Self-reported difficulty in accessing the pedagogical platform for the Int-EL group and the access to the documents for the Pass-EL group.
Time Frame: one month
|
"easy", "medium to difficult" and "difficult"
|
one month
|
|
Self-reported difficulty to validate the MCQs felt by the students of the Int-EL group.
Time Frame: one month
|
"easy", "medium to difficult" and "difficult"
|
one month
|
|
Self-reported e-learning usage between the two e-learning groups of the means.
Time Frame: One month
|
The reporting time of e-learning usage was in minutes
|
One month
|
|
Student satisfaction score between the two e-learning groups
Time Frame: One month
|
Satisfaction score ranging from 0 to 10.
|
One month
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E2015-53
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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