ClinicalTrials.gg
CompletedNCT034785793D-QUAMUUpdated Feb 3, 2022

Non-technical Skills of Emergency Physicians in a Virtual Emergency Department

An observational study in Emergencies, sponsored by University Hospital, Toulouse. Completed at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-02-03.

Primary conditionnone(registry's first term: Emergencies)No conditionIs this wrong?Emergencies describes something many studies share rather than a condition a study is about. The study names no condition we can place it under, so it is not compared with other studies by condition.

Sponsored by University Hospital, Toulouse · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
18 Years and older
Sex
All
01

Study summary

The investigators will study nontechnical skills of emergency physicians in a virtual standardized emergency room and their impact on quality of care.

Read the detailed description

The ability to manage multiple patients and anticipate the risk of error related to task interruptions or disruptions has been identified among relevant non-technical skills (NTS) for practicing emergency medicine. However, the link between these skills and the quality of care has not been quantified. NTS are usually analyzed by qualitative methods such as interviews, direct observations, or questionnaires that have low performance according to the GRADE system (Grading of Recommendations, Assessment, Development and Evaluation).

The investigators have created and validated an experimental model of a virtual, authentic and realistic Emergency Department (ED). The platform has been modelled in a "Second Life" environment. The NTS of emergency physicians will be assessed and recorded during simulated care of multiple virtual patients. The NTS association with ED length of stay and disposition decision will be analyzed. This study will be an internal pilot study and will include 30 emergency physicians who practice emergency medicine for at least two years.

Sessions will be performed in the Toulouse Institute of Health Care Simulation, Toulouse University Hospital. They will be composed of three stages: briefing (30 minutes), simulated practice (3 hours), and debriefing with an explicit interview (30 minutes). Two researchers and a computer technician will supervise the sessions. The data will be obtained by analyzing the video recorded during the simulated practice and the interview.

02

Conditions studied

  • Emergencies

Browse trials for

Keywords

  • serious game
  • simulation
  • virtual emergency department
  • nontechnical skills
03

In context

Lead sponsor

University Hospital, Toulouse is the lead sponsor of 807 studies on the registry; 209 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Emergency physicians working in the French Midi-Pyrénées region

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Active emergency physicians working in an ED of the French Midi-Pyrenees region
  • Two years of practice in emergency medicine or more
  • Volunteer to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Emergency physician working in another setting than ED, outside the Midi-Pyrenees region, or practicing emergency medicine for less than 2 years.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (actual)
Patient registry
No

Groups and cohorts

  • Emergency physicians

    The observational group will be composed of emergency physicians working in the French Midi-Pyrenees region. Physicians must work since 2 years in emergency service

    Other: observational

Interventions

  • Otherobservational

    No intervention, it is observational study

06

What researchers measure

Primary outcomes

  1. Nontechnical skills

    The nontechnical skills will be assessed by the Anaesthetists' Non-Technical Skills (ANTS) system.

    Time frame: 3 hours

Secondary outcomes

  1. Quality of care will be measured by a composite criteria (process and result)

    Quality of care will be measured by a composite criterion associating a process indicator and a result indicator : * The process indicator is the average time to medical care of patients * The result indicator corresponds to the relevance of the choice of the orientation of each patient by the emergency doctor at the end of medical care

    Time frame: 3 hours

  2. ED length of stay

    The quality of care will be assessed by ED length of stay : ED length of stay will be measured from triage completion to disposition decision

    Time frame: 3 hours

  3. The authenticity of the virtual emergency medicine service

    Evaluation of the consistency : perceived internal consistency in the proposed rules and situations will be assessed using a 4-item questionnaire by answering yes or no

    Time frame: 3 hours

  4. The authenticity of the virtual emergency medicine service

    Evaluation of the realism (the assumed resemblance with a real life reference) will be evaluated through a questionnaire containing 3 areas of comparison between the virtual and real environment (layout of the premises, duration of the actions, staff / patient ratio) with as answer possible for each comparison: Realistic or not realistic.

    Time frame: 3 hours

  5. The authenticity of the virtual emergency medicine service

    Evaluation of the relevance (necessary to allow users to take ownership of the problems posed by the designers) will be assessed through direct observation with a yes / no evaluation of the acceptance to use the virtual environment, to test the environment, to make choices during the scenario and to control the environment.

    Time frame: 3 hours

07

Study locations

1 site
  • CHU Toulouse
    Toulouse, 31059, France
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 Feb 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03478579
Responsible party
Sponsor
First posted
Mar 27, 2018
Start date
Jun 1, 2018
Primary completion
Sep 1, 2019
Completion
Dec 1, 2020
Last update
Feb 3, 2022

Study contacts

Dominique Lauque, MD
study chair · Toulouse CHU

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 completed, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion