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Not yet recruitingNCT07110012STRAICUpdated Aug 7, 2025

The Role of Simulation-based Training in Resident Curriculum in Anaesthesia and Intensive Care

An observational study in Simulation Training, Education and Critical Care, Intensive Care, sponsored by Brno University Hospital. Not yet recruiting. Per ClinicalTrials.gov, last updated 2025-08-07.

Sponsored by Brno University Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Nov 2025, 10 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
200
Sex
All
01

Study summary

This observational study aims to describe the situation in Europe regarding simulation training during residency in Anaesthesia and Intensive Care. The main questions it aims to answer are:

How many countries in Europe have obligatory simulation training during residency? How frequent is this training? What and how is trained during simulations? How is the situation regarding funding and participation in working hours in simulation training? What are the obstacles for the countries that do not have obligatory training? Participants will fill out an electronic survey.

Read the detailed description

Postgraduate education is frequently discussed in various aspects. Simulations are modern and effective tools for medical education and training during residency in Anaesthesia and Intensive Care, and are no exception. Three years ago, the survey mapped the situation of simulation-based training as an obligatory part of the residency curriculum. Now, we would like to describe the progress and identify possible factors that are preventing the further spread of simulations into postgraduate education.

02

Conditions studied

  • Simulation Training
  • Education
  • Critical Care, Intensive Care
  • Anaesthesia

Keywords

  • simulation training
  • intensive care
  • European survey
  • education
  • physicians
  • Anesthesia
03

In context

Lead sponsor

Brno University Hospital is the lead sponsor of 91 studies on the registry; 22 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
No
Sampling method
Non-probability sample

Study population

ESAIC NASC representatives. These are clinicians representing their countries in European National Societies of Anaesthesiologists of the European Society of Anaesthesiology and Intensive Care.

Inclusion criteria

  • ESAIC NASC representatives.

Exclusion criteria

Exclusion Criteria:

  • not ESAIC NASC representatives.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
200 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. How many European countries have some type of simulation training included in the postgraduate curriculum?

    This study aims to explore how many European countries have some sort of simulation included in postgraduate training. The optional or obligatory training both included.

    Time frame: 3 monts.

  2. How many European countries have obligatory simulation training in Anaesthesia and Intensive Care?

    This study aims to explore the prevalence of obligatory simulation training in postgraduate training in Anaesthesia and Intensive Care.

    Time frame: 3 months

Secondary outcomes

  1. How extensive is the simulation training in Anaesthesiology and Intensive Care in European countries?

    The study aims to explore how many days of simulation training are obligatory or advised to undergo during the postgraduate training in Anaesthesia and Intensive Care.

    Time frame: 3 monts

  2. What role does AI play in simulation training?

    The study aims to explore the role of AI in simulation training in Anaesthesia and Intensive Care in Europe.

    Time frame: 3 months.

  3. Specification of simulation training

    This study aims to describe what simulation modalities (low fidelity simulation, high fidelity simulation, etc.) are used in different European countries. Also, the themes covered by simulation training are explored.

    Time frame: 3 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 7, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07110012
Lead sponsor
Brno University Hospital
Collaborators
Masaryk University
Responsible party
Tereza Prokopova, MD (MD, PhD., Brno University Hospital) — Principal investigator
First posted
Aug 7, 2025
Start date
Sep 1, 2025 (estimated)
Primary completion
Nov 30, 2025 (estimated)
Completion
Dec 30, 2025 (estimated)
Last update
Aug 7, 2025

Study contacts

Tereza Prokopová, MD,PhD.
Contact
prokopova.tereza@gmail.com
+420736669784

Oversight

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

Not currently enrolling

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

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