- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07886866
The Effect of Virtual Reality-Based Disaster Training on Disaster Readiness of Health Science Students (VR-DT-DRHSS)
This study evaluated the effect of three-dimensional (simulations) virtual reality-based disaster training with simulation on disaster readiness among health science students. The study used a randomized controlled design. Participants assigned to the intervention group received disaster training using 3D virtual reality technology and simulation, while participants in the control group received usual education or training. Outcomes were assessed at baseline before the intervention, after completion of the training, and at a subsequent follow-up assessment. The study aimed to evaluate the effects of simulations virtual reality-based simulation training on disaster readiness over time.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Disaster readiness is an important competency for health science students, who may be required to contribute to healthcare responses during emergencies and disasters. Educational strategies that combine practical learning with simulated scenarios may help students develop the preparedness needed to respond to disaster situations.
Three-dimensional (simulations) virtual reality technology combined with simulation provides an immersive learning environment in which students can engage with simulated disaster scenarios. This approach allows students to experience disaster-related situations in a controlled educational setting.
This randomized controlled study evaluated the effect of simulations virtual reality-based disaster training with simulation on disaster readiness among health science students. Participants were randomly assigned to an intervention group or a control group. The intervention group received simulations virtual reality-based disaster training with simulation, while the control group received usual education or training.
Study outcomes were assessed before the intervention, after the training, and at a subsequent follow-up assessment using the measurement instruments specified in the study protocol. The study examined whether the intervention affected disaster readiness and whether any observed effects were maintained at follow-up after 8 week.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
-
Riyāḑ, Arabie Saoudite, 3422
- Vision Colleges
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
Students enrolled in the participating health sciences programs at the study institution.
Students who met the study's age and participation requirements.
Students who provided informed consent to participate.
Exclusion Criteria:
- Students who did not meet the inclusion criteria.
Students who declined to participate or did not provide informed consent.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Virtual Reality-Based Disaster Training
Participants received disaster training using simulations virtual reality technology and simulation |
Participants in the intervention group received disaster training using three-dimensional virtual reality technology and simulation. The training was designed to provide an immersive learning experience involving disaster scenarios to support disaster readiness among health science students. The intervention was delivered according to the study protocol. |
|
Aucune intervention: Usual Education or Training
Participants received disaster training without using simulations virtual reality technology and simulation |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Disaster Preparedness Skills
Délai: Baseline before the intervention to immediately after completion of training.
|
Disaster preparedness skills will be assessed using the Disaster Preparedness Skills Form (DPSF). The minimum possible score is 0, and the maximum possible score is 25. Higher scores indicate better disaster preparedness skills. |
Baseline before the intervention to immediately after completion of training.
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Disaster Preparedness Skills at 8-Week Follow-Up
Délai: 8 weeks after completion of the training.
|
Disaster readiness skills will be assessed using the Disaster Preparedness Skills Form (DPSF), the same measurement instrument used for the baseline and post-training assessments. The minimum possible score is 0, and the maximum possible score is 25. Higher scores indicate better disaster preparedness skills. |
8 weeks after completion of the training.
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- #H-02-J-126
- H-02-J-126 (Autre identifiant: Vision Colleges)
Informations sur les médicaments et les dispositifs, documents d'étude
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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 .