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The DREAM-VR Study: Does a Virtual Reality Tool Help Dental Students Master Acute Medical Emergencies Better? (DREAM-VR)

3 septembre 2026 mis à jour par: Denise van Diermen

The DREAM-VR Study: Dental Students' Readiness for Emergency Assessment and Management Through Virtual Reality

The goal of this prospective educational cross-over study is to compare the competency and self-reported confidence in managing acute medical emergencies in fourth year dental students at the Academic Centre for Dentistry (ACTA) after training with a Virtual Reality (VR) training tool. The main questions it aims to answer are:

  • Do students who were trained with the VR tool perform better or equally good as students who were trained with a traditional training, in managing acute medical emergencies?
  • Do students who were trained with the VR tool score higher in self-reported confidence scores? Researchers will compare the group who trained with the VR tool with a group who received a traditional training with a mannikin to see if students from one of these methods performs better at a clinical exam in managing an acute emergency that is played by a trained actor. They will also be compared with themselves, since after 4 weeks the groups will be crossed-over and will receive the other training with different clinical scenarios.

Half of the participants will

  • In week 1-4:
  • Play a VR scenario and watch peer students play other VR scenario's
  • Fill out a written peer-feedback form and discuss this with peers
  • Fill out 3 short online questionnairs, before the training, just before the formative clinical exam and just after the formative clinical exam
  • Participate in a formative clinical exam with a trained actor
  • In week 5-8:
  • Play a scenario with a mannikin and watch peer students play other scenario's*
  • Fill out a written peer-feedback form and discuss this with peers
  • Fill out 2 short online questionnairs, just before the summative clinical exam and just after the summative clinical exam
  • Participate in a summative clinical exam with a trained actor* The other half of the participants will participate in the same protocol, but in the reverse order. They start with the traditional training with a mannikin in week 1-4 and cross-over to VR in week 5-8.

    • The training program with a mannikin and the summative clinical exam is part of the regular curriculum.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

140

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Denise E van Diermen, MD, PhD
  • Numéro de téléphone: +31 20 5980654
  • E-mail: d.v.diermen@acta.nl

Sauvegarde des contacts de l'étude

  • Nom: Marije Petersen, MD, Dentist, PhD
  • Numéro de téléphone: +31 20 5980654
  • E-mail: j.f.petersen@acta.nl

Lieux d'étude

    • North Holland
      • Amsterdam, North Holland, Pays-Bas, 1081 LA
        • Academic Center for Dentistry Amsterdam

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • 4th year dental students at ACTA who participate in the course Medical Dental Interaction in september-october 2026

Exclusion Criteria:

  • students who experience severe side-effects of the VR tool, such as severe dizziness, nausea or headche
  • students who do not provide informed consent

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: VR group
Dental students that practice with a VR tool for managing acute medical emergencies
Students are immersed in a virtual dental clinic. They see a virtual patient in the dental chair (avatar). The avatar can be controlled by the teacher to show signs of acute medical emergencies. The student can talk to the avatar, the avatar can talk back. The student can use virtual tools, such as blood pressure device, oximeter, etc. to diagnose the emergency and can apply virtual medication such as epinephrine injection, oxigen, etc. They can play 7 different scenario's: fainting, asthma attack, anaphylaxis, stroke, heart attack, epilepsy, hypoglycemia. They can call 911/112 to ask for an ambulance and can do a medical handover to the ambulance personell.
Comparateur actif: Mannikin group
Dental students that practice with a resuscitation mannikin for managing acute medical emergencies.
Students are told by the teacher that the mannikin is a dental patient that experiences an acute medical emergency, and what the patients' complaints are. The students can use diagnostic devices, such as blood pressure tool and oximeter, to practice. The teacher tells what the outcome of measurement is and the student proposes a diagnosis and treatment plan. They can give the mannikin test medication such as epinehrin or oxigen.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Competence in diagnosing and treating acute medical emergencies in the dental practice
Délai: From enrollment assessment takes place in Week 4 and week 8

In week 4 the students will do a formative clinical test with a trained actor, who plays an acute medical emergency scenario. The topic of the scenario will be randomly assigned by drawing a lot. The students will be scored using a validated scoring table, that measures all the necessary steps in the DRS ABCDE protocol. They can obtain a maximum score of 80 when they do all the necessary steps to manage the acute emergency.

Again in week 8 the students will do a summative clinical test with a trained actor. The topic of the scenario be randomly assigned. The students will be scored using the same validated scoring table. They will pass the test if they used the adequate diagnostic tools, made the correct diagnosis and communicated effectively with the ambulance personnel. The point score on the scoring table will only be used for research purposes.

From enrollment assessment takes place in Week 4 and week 8
Self-reported competence in managing acute medical emergencies
Délai: From enrollment until week 4 and 8

Students will be asked to fill out 5 online surveys to report on their experienced sense of competence. The questions will be on a 5 point likert scale.

T=0: before enrolling in the training T=1: just before the formative clinical test in week 4 T=2: just after the formative clinical test in week 4 T=3: just before the summative clinical test in week 8 T=4: just after the summative clinical test in week 8

From enrollment until week 4 and 8
Self-reported confidence in managing acute medical emergencies
Délai: From enrollment in week 4 and 8

Students will be asked to fill out 5 online surveys to report on their experienced sense of confidence. The questions will be on a 5 point likert scale.

T=0: before enrolling in the training T=1: just before the formative clinical test in week 4 T=2: just after the formative clinical test in week 4 T=3: just before the summative clinical test in week 8 T=4: just after the summative clinical test in week 8

From enrollment in week 4 and 8

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Effects of order and carry-over effects in the cross-over design
Délai: From enrollment until week 8
To assess whether the order in which participants receive the virtual reality training and the comparator training affects outcome scores, and whether exposure to the first intervention has a residual effect on outcomes measured after the second intervention. Intervention sequence (VR-first versus comparator-first), study period, and prior intervention exposure will be evaluated in a mixed-effects model, accounting for repeated measurements within participants.
From enrollment until week 8

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Students' subjective experiences with the use of the VR tool
Délai: From enrollment until week 8
A short online questionnaire with closed questions with a 5 point Liket scale and open questions will evaluate the subjective experiences and feedback of the students who participated in the study
From enrollment until week 8

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Denise E van Diermen, MD, PhD, Academic Centrer for Dentistry Amsterdam

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

31 août 2026

Achèvement primaire (Estimé)

31 octobre 2026

Achèvement de l'étude (Estimé)

31 octobre 2026

Dates d'inscription aux études

Première soumission

30 août 2026

Première soumission répondant aux critères de contrôle qualité

3 septembre 2026

Première publication (Réel)

10 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

10 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

3 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 2026-54154

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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