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NOT YET RECRUITING
NCT06916949
NA

Stress Evaluation and Management Using High Fidelity Simulation in Medical Education

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS

View on ClinicalTrials.gov

Summary

The goal of this interventional study is to collect clinical and neurophysiological information to determine whether high-fidelity simulation can serve as a stress-inducing stimulus in a population of healthy residents (Emergency medicine, Anesthesia and Intensive care medicine, Paediatrics), both male and female, aged between 25 and 40 years. The main questions it aims to answer are: 1. Define in which phase of the simulation the highest level of stress is observed. 2. Determine the level of stress reached after performing a second high-fidelity simulation after a period of time. 3. Identify whether specific brain areas are activated during high-fidelity simulation. Participants will form teams, consisting of three medical trainees from the same specialty training program, that will undergo two high-fidelity simulations based on a clinical scenario relevant to their residency. * During the simulation, automatic pupillometry will be performed on all team members at the four time points. * Additionally, a two-lead ECG will be recorded for all team members at baseline and end of the debriefing * One team member will undergo EEG monitoring throughout the entire simulation. The EEG recordings will be sampled at baseline, during the simulation and end of the debriefing.

Official title: The Role of High-fidelity Medical Simulation in Managing Emotional Components and Stress During Emergency and Urgent Care

Key Details

Gender

All

Age Range

25 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

45

Start Date

2025-04

Completion Date

2025-05

Last Updated

2025-04-08

Healthy Volunteers

Yes

Interventions

DIAGNOSTIC_TEST

Electrocardiogram

two leads ECG

DIAGNOSTIC_TEST

Pupillometry

During the simulation, automatic pupillometry will be performed on all team members at the following time points: Baseline (T0) During the simulation (T1) End of the simulation (T2) End of the debriefing (T3)

DIAGNOSTIC_TEST

Electroencephalogram

EEG monitoring throughout the entire simulation. The EEG recordings will be sampled at: Baseline (T0) During the simulation (T1) End of the debriefing (T2)