CClinicalTrials.gg
CompletedNCT07121400Updated Aug 13, 2025

E-learning Teaching During Anesthesia Residency

An interventional study of Interactive e-learning-group in Learning, Anesthesia and Resident Education, sponsored by University Hospital, Rouen. Completed. Per ClinicalTrials.gov, last updated 2025-08-13.

Sponsored by University Hospital, Rouen · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 9 years 5 months after the study started (first participant enrolled Feb 2016, registered Jul 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
54
Allocation
Randomized
Sex
All
01

Study summary

E-learning is in expansion although its pedagogical performance has not been validated in the anesthesia residency. E-learning can be divided into passive e-learning; guided e-learning, interactive e-learning, and adaptive e-learning. The objective was to compare the impact of passive e-learning versus interactive e-learning on anesthesia residents' acquisition of theoretical knowledge and clinical reasoning.

Read the 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.

02

Conditions studied

  • Learning
  • Anesthesia
  • Resident Education

Keywords

  • E-learning
  • anesthesia residency
  • resident education
  • computer-assisted learning
  • clinical knowledge assessment
03

In context

Lead sponsor

University Hospital, Rouen is the lead sponsor of 410 studies on the registry; 104 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • All anesthesiology residents from first to fourth year in both centers (participants)

Exclusion criteria

Exclusion Criteria:

  • Exclusion criteria included residents missing the pre-or post-tests or refusing to participate in the training program.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
54 participants (actual)

Study arms

  • 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.

    Procedure: Interactive e-learning-group

Interventions

  • ProcedureInteractive e-learning-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.

06

What researchers measure

Primary outcomes

  1. Comparison of the theoretical clinical knowledge score between the two e-learning groups

    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.

    Time frame: One month after pre-test

Secondary outcomes

  1. The comparison of clinical reasoning scores between the two e-learning groups

    Evaluated by the paired within-subject differences (delta) SCT scores (pre-and post-test). The score could range from 0 to 50 points.

    Time frame: one month

  2. Self-reported difficulty in accessing the pedagogical platform for the Int-EL group and the access to the documents for the Pass-EL group.

    "easy", "medium to difficult" and "difficult"

    Time frame: one month

  3. Self-reported difficulty to validate the MCQs felt by the students of the Int-EL group.

    "easy", "medium to difficult" and "difficult"

    Time frame: one month

  4. Self-reported e-learning usage between the two e-learning groups of the means.

    The reporting time of e-learning usage was in minutes

    Time frame: One month

  5. Student satisfaction score between the two e-learning groups

    Satisfaction score ranging from 0 to 10.

    Time frame: One month

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Selim J, Thill J, Burey J, Besnier E, Lambert M, Lefevre-Scelles A, Abily J, Gastaldi G, Allard E, Hanouz JL, Veber B, Dureuil B, Thill C, Compere V. Pedagogical impact of different levels of e-learning teaching during anesthesia residency: a randomized clinical trial. BMC Med Educ. 2026 Apr 29;26(1):971. doi: 10.1186/s12909-026-09225-4. PubMed 42056999 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07121400
Lead sponsor
University Hospital, Rouen
Responsible party
jean.selim (Doctor, University Hospital, Rouen) — Principal investigator
First posted
Aug 13, 2025
Start date
Feb 1, 2016
Primary completion
Jun 30, 2016
Completion
Jun 30, 2016
Last update
Aug 13, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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