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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05960747
Acronym
ARPEGES
Enrollment
340
Registered
2023-07-27
Start date
2024-02-15
Completion date
2026-02-28
Last updated
2025-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frist Time Indication to Perform a Thoracentesis, Medical Student Training, Pleural Effusion

Keywords

Thoracentesis, Augmented virtual reality simulator, Medical student training

Brief summary

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.

Interventions

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

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Medical students : Inclusion criteria: * 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).

Exclusion criteria

\- Student with a prior experience of pleural procedure (chest tube, thoracocentesis). Patients : Inclusion criteria: * Patients requiring a first-time thoracentesis in routine care. * Older than 18 years old. * Speaking and understanding French. * Valid health insurance. * No opposition to participate to the study (signed consent form).

Design outcomes

Primary

MeasureTime frameDescription
Assessment of the success rate1 dayAssessment 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

Secondary

MeasureTime frameDescription
Assessment of specific characteristic prior and after thoracocentesis1 dayAssessment of specific characteristic prior and after thoracocentesis for the patient (pain, anxiety), and for the medical student (theorical knowledge, anxiety, ability during the procedure.

Countries

France

Contacts

Primary ContactBenjamin RENAUD-PICARD
benjamin.renaudpicard@chru-strasbourg.fr+33 3.68.55.01.82
Backup ContactMaxime FURSTENBERGER
maxime.furstenberger@chru-strasbourg.fr+33 3 69.55.06.45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026