ClinicalTrials.Veeva

Menu

Trial of Multidisciplinary Team Stress and Performance in Immersive Simulation for Management of Infant in Shock

P

Poitiers University Hospital

Status

Completed

Conditions

Stress

Treatments

Other: MDT simulation sessions of management of life-threatening events over 1 year

Study type

Interventional

Funder types

Other

Identifiers

NCT02424890
Sim-stress.1

Details and patient eligibility

About

The objective of this randomized trial is to study the effect of stress on performance and the effect of repetition of simulation sessions on performance and stress. This study is a randomized controlled trial including 48 participants who composed 12 multidisciplinary teams (MDTs). Each MDT was made up of 4 persons: an emergency physician, a resident, a nurse, and an ambulance driver who usually compose an emergency team of the French Emergency Medical Service (EMS). 6 MDTs underwent 9 simulation sessions over 1 year (Repetitive SIm Group). 6 MDTs underwent 3 simulation sessions over 1 year (Control Group). Evidence of the existence of stress was assessed in 3 ways: salivary cortisol, Holter parameters, and psychological stress questionnaires. The impact of stress on overall team performance, on technical procedure, and on teamwork, is evaluated by specific validated scales. Detection of post-traumatic stress (PTSD) is performed by self-evaluation on the 7th day and after one month. The perspective is to concomitantly evaluate technical and non-technical performance, and the impact of stress on both. This is the first randomized trial studying repetition of simulation sessions and its impact on both clinical performance and stress as explored by objective and subjective assessments. The investigators expect that stress decreases team performance and that repeated simulation increases team performance. The investigators expect no variation of stress parameters regardless of level of performance.

Enrollment

48 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Multidisciplinary team made up of 4 persons:

    1. an emergency physician with less than seven years of experience ,
    2. a resident,
    3. a nurse,
    4. and an ambulance driver.

Exclusion criteria

  • Past history and/or psychiatric disease that modifies stress response,
  • Pacemaker or implantable defibrillator,
  • Treatment with a medication having a potential effect on stress parameters.

Trial design

48 participants in 2 patient groups

Repetitive Sim Group
Active Comparator group
Description:
9 simulation sessions
Treatment:
Other: MDT simulation sessions of management of life-threatening events over 1 year
Control Group
Active Comparator group
Description:
3 simulation sessions
Treatment:
Other: MDT simulation sessions of management of life-threatening events over 1 year

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems