NCT07771569

Brief Summary

This study aims to describe the current implementation and structure of simulation-based education and training in anaesthesiology and intensive care residency programmes across countries affiliated with the World Federation of Societies of Anesthesiologists.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
9mo left

Started Oct 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Oct 2026Jun 2027

First Submitted

Initial submission to the registry

August 12, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 18, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2027

Last Updated

August 18, 2026

Status Verified

August 1, 2026

Enrollment Period

7 months

First QC Date

August 12, 2026

Last Update Submit

August 15, 2026

Conditions

Keywords

simulationeducationanaesthesiaintensive caresurvey

Outcome Measures

Primary Outcomes (2)

  • How many countries affiliated with WFSA have some type of simulation training included in the postgraduate curriculum?

    Number of WFSA-affiliated countries with obligatory training or optional training.

    3 months

  • How many countries affiliated with WFSA have obligatory simulation training in Anaesthesia and Intensive Care?

    Prevalence of obligatory simulation training in postgraduate training in Anaesthesia and Intensive Care.

    3 months

Secondary Outcomes (5)

  • What is required of the HCP to be able to provide anaesthesia unsupervised worldwide?

    3 months

  • How extensive is the simulation training in Anaesthesiology and Intensive Care in countries affiliated with WFSA?

    3 months

  • Specification of simulation training

    3 months

  • What are the major barriers limiting the wider implementation of simulation-based education in anaesthesia residency training in countries affiliated with WFSA?

    3 months

  • What role do artificial intelligence and virtual reality play in simulation training?

    3 months

Study Arms (3)

Representatives of their countries in WFSA

Representatives of regional sections

Representatives of corresponding members

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

WFSA representatives. These are clinicians representing their countries, regional sections or corresponding member societies in the World Federation of Societies of Anesthesiologists (WFSA).

You may qualify if:

  • WFSA representatives.

You may not qualify if:

  • not WFSA representatives.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Masaryk University

Brno, Česká Republika, 62500, Czechia

Location

Related Publications (1)

  • Savoldelli GL, Ostergaard D. Simulation-based education and training in anaesthesia during residency in Europe: where are we now?: A survey conducted by the European Society of Anaesthesiology and Intensive Care Simulation Committee. Eur J Anaesthesiol. 2022 Jun 1;39(6):558-561. doi: 10.1097/FJA.0000000000001667. Epub 2022 Feb 21. No abstract available.

    PMID: 35608878BACKGROUND

Study Officials

  • Petr Štourač, prof., MD.,Ph.D., FESAIC

    Department of Simulation Medicine, Faculty of Medicine, Masaryk University, Brno, Czech Republic

    STUDY DIRECTOR

Central Study Contacts

Tereza Prokopová, MD,PhD.

CONTACT

Jan Hudec, MD, Ph.D.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

August 12, 2026

First Posted

August 18, 2026

Study Start

October 1, 2026

Primary Completion (Estimated)

April 30, 2027

Study Completion (Estimated)

June 30, 2027

Last Updated

August 18, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations