Improvement to Perform Thoracocentesis After a Specific Training in Medical Students With the Supervised Use of an Augmented Reality Simulator

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Strasbourg, France

About this trial

Monocentric study, aiming to assess the improvement of medical students to perform a first-time thoracentesis after training using a specific training using an augmented virtual reality simulator, versus standard training.

Study population: medical students from the department of Respirology (University hospital of Strasbourg), performing their first thoracocentesis in patients having an indication for a first-time thoracocentesis.

This is not an interventional study, no change in patient course being induced because of the study.

After the procedure: use of specific surveys for the patient and for medical students to assess the patient's pain, the patient and the medical student level of anxiety, and the student ability during the procedure.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Medical students between the 4th and 6th year of their medical course, working in the department of respirology at the University hospital of Strasbourg, France, without any prior experience of thoracocentesis.

Older than 18 years old

No opposition to participate to the study (signed consent form).

Disqualifiers

Patients requiring a first-time thoracentesis in routine care.

Older than 18 years old.

Speaking and understanding French.

Valid health insurance.

Trial population

* Medical students between the 4th and 6th year of their medical course, working in the department of respirology at the University hospital of Strasbourg, France, without any prior experience of thoracocentesis. * Patients requiring a first-time thoracentesis in routine care

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Simulation group

    Other intervention

    Specific training for medical students by using an augmented virtual reality simulator for thoracentesis

Treatment groups

340 Participants
are divided into 2 treatment groups
Group A: Control group0 interventions
Group B: Simulation group1 intervention

Trial outcomes

Primary outcomes

1

Assessment of the success rate

Assessment of the success rate to perform a first-time thoracentesis in patients with an indication for this procedure, depending on whether the medical student was trained using an augmented virtual reality simulator, or with standard training

Time frame
1 day

Secondary outcomes

1

Assessment of specific characteristic prior and after thoracocentesis

Assessment of specific characteristic prior and after thoracocentesis for the patient (pain, anxiety), and for the medical student (theorical knowledge, anxiety, ability during the procedure.

Time frame
1 day

Other outcomes

Sponsors and contacts

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