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SST in Emergency Education (SST)

The Application of Scenario Simulation Teaching and Confidence Behavior Evaluation in Emergency Medicine Teaching

This study looks back at how the investigatorsll two different teaching methods work for training medical and nursing students in CPR (cardiopulmonary resuscitation), a life-saving emergency procedure used when someone's heart stops. the investigators want to find out whether learning through realistic emergency case simulations helps students gain better skills and knowledge than traditional classroom lectures.

The study reviews training records of medical and nursing interns-students in their first hands-on hospital training-who completed CPR training betthe investigatorsen September 2024 and November 2025. the investigators included students who had no prior CPR certification and who attended most of their training sessions.

Because this is a retrospective study, no one needs to take part in any new activities or visits. Researchers will analyze existing training records, test scores, and anonymous survey responses that the investigatorsre already collected during past training sessions. One group of students learned CPR through traditional lectures and instructor demonstrations. The other group learned through hands-on case-based simulations, where they practiced working together as a medical team in realistic emergency scenarios.

This research may help hospitals choose better ways to teach CPR to future doctors and nurses. If case-based simulation proves more effective, more students could receive this type of training, which may help them respond more confidently and effectively in real-life emergencies. Ultimately, better-prepared healthcare professionals may improve care for patients experiencing cardiac arrest.

There are no direct risks to participants. The study only uses existing anonymous teaching records, and no personal identities will be shared in any study reports.

Aperçu de l'étude

Statut

Complété

Description détaillée

Clinical clerkship in emergency medicine represents a critical transition period for medical students, bridging the gap from theoretical knowledge to practical application. The traditional "didactic lecture + bedside teaching" model has the investigatorsll-documented limitations, including disconnection betthe investigatorsen theory and practice, passive student engagement, and insufficient training in clinical reasoning.

In recent years, innovative pedagogical models-such as the Flipped Classroom (FC) combined with the SNAPPS structured clinical reasoning framework, and Case-Based Scenario Simulation Teaching (CBSST)-have demonstrated promising outcomes in emergency and critical care medical education. While traditional lecture-based instruction falls short in fostering active learning and critical thinking, case-based scenario simulation immerses learners in highly realistic clinical contexts, enabling interns to experience the urgency of emergency care before actual clinical practice and to master the core elements of team-based resuscitation.

Entrustable Professional Activities, EPAs has gained increasing recognition in healthcare training. Simulation-based collaborative training betthe investigatorsen medical and nursing students improves role clarification, facilitates task coordination, and narrows knowledge-system gaps betthe investigatorsen disciplines. Hothe investigatorsver, existing studies have largely focused on general clinical skills rather than specifically targeting CPR scenarios involving collaborative medical-nursing intern teams. Furthermore, there is a paucity of systematic evaluations regarding the effectiveness of case-based scenario simulation in this specific context.

Previous single-center randomized controlled trials have shown that the FC+SNAPPS model significantly improves interns' theoretical knowledge, Mini-CEX clinical core competencies (history taking, physical examination, clinical assessment, and clinical judgment), and teaching satisfaction. Similarly, CBSST has been shown to simultaneously enhance theoretical scores, procedural skills, clinical judgment, and teamwork among medical and nursing interns during CPR training. Nevertheless, current research remains limited in several aspects:

  1. Limited evaluation dimensions: Most studies rely on immediate theoretical examinations and Mini-CEX skill scores as primary outcomes, lacking assessment of whether trainees "can be trusted to perform professional activities independently"-a core competency indicator.
  2. Insufficient model comparison: Existing studies predominantly compare a single innovative model against conventional instruction, with little direct comparison betthe investigatorsen different innovative models or exploration of synergistic effects.
  3. Limited external validity: Single-center, small-sample designs restrict generalizability.
  4. Unknown long-term effects: There is a lack of longitudinal follow-up regarding knowledge retention, skill maintenance, and clinical entrustment decision-making capacity.

Entrustable Professional Activities (EPAs) represent a competency-based core assessment framework in medical education, emphasizing supervising physicians' entrustment decisions regarding whether a learner can independently execute a specific clinical activity. EPA evaluation extends beyond "can they do it" (knowledge and skills) to encompass trust and behavioral competence, aligning closely with the high-risk, practice-intensive nature of emergency medicine. Incorporating EPA as a guiding evaluation tool can compensate for the limitations of traditional Mini-CEX in assessing "independent decision-making and responsibility-bearing," thereby providing more clinically practical evidence for teaching model reform.

Type d'étude

Observationnel

Inscription (Réel)

69

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.

Lieux d'étude

      • Hangzhou, Chine
        • The Second Affiliated Hospital of Zhejiang University School of Medicine

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

Non

Méthode d'échantillonnage

Échantillon de probabilité

Population étudiée

Enrolled 69 medical and nursing interns rotating at our hospital from September 2024 to November 2025.

La description

Inclusion Criteria:

  • First-time clinical internship;
  • No prior BLS certification;
  • Attendance rate ≥ 90%.

Exclusion Criteria:

  • Leave of absence ≥10% during the training period;
  • Withdrawal from the study for other reasons after enrollment.

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

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
control group
Received conventional lecture-based CPR training.
intervention group
received case-based scenario simulation teaching with interprofessional team training, consisting of five stages
The intervention group received case-based scenario simulation teaching with interprofessional team training, consisting of five stages

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
theoretical exam
Délai: up to 2 weeks
The assessment included a theoretical exam (maximum score: 100 points)
up to 2 weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Mini-CEX Scores
Délai: up to 2 weeks
Prior to the study, both assessors participated in a 2-hour calibration session reviewing standardized Mini-CEX rating criteria and benchmark video recordings. Inter-rater reliability was assessed using Cohen's kappa coefficient based on 10 independently scored pilot cases. The kappa value was 0.85 (95% CI: 0.72-0.98), indicating excellent agreement between the two assessors. The Mini-CEX scoring system uses a three-level, 9-point scale, which is categorized as follows: Needs Improvement (1-3 points, indicating very poor, poor, and average), Pass (4-6 points, indicating good, moderate, and fair), and Excellent (7-9 points, indicating excellent, very good, and exceeding expectations). This evaluation system covers four dimensions: knowledge mastery, operational skills, clinical judgment, and team collaboration, with a maximum score of 36 points
up to 2 weeks
Questionnaire Survey
Délai: up to 2 weeks

The satisfaction questionnaire was developed based on established dimensions of instructional design and learner engagement identified in health professions education literature[8], and adapted for the specific context of CPR simulation training. Content validity was ensured through review by a panel of three clinical education experts (including BLS instructors and medical educators), who evaluated the relevance, comprehensiveness, and representativeness of the five dimensions (course content, course resources, classroom interaction, teaching methods, and learning burden) and confirmed that all items adequately reflected the constructs of interest in simulation-based CPR education.

Prior to formal administration, the questionnaire underwent pilot testing with 10 medical and nursing interns who were not included in the main study sample. The pilot test confirmed the clarity of item wording, logical flow of dimensions, and appropriateness of the 5-point rating scale. Internal consisten

up to 2 weeks

Collaborateurs et enquêteurs

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

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 (Réel)

1 septembre 2024

Achèvement primaire (Réel)

30 novembre 2025

Achèvement de l'étude (Réel)

30 décembre 2025

Dates d'inscription aux études

Première soumission

25 août 2026

Première soumission répondant aux critères de contrôle qualité

31 août 2026

Première publication (Réel)

4 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

4 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

31 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 2026-0693
  • 20230242,20240410 (Autre subvention/numéro de financement: Teaching reform research and cultivation project of The Second Affiliated Hospital of Zhejiang University School of Med)

Plan pour les données individuelles des participants (IPD)

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

NON

Description du régime IPD

Due to institutional data privacy policies and the retrospective use of anonymized teaching records, individual participant data cannot be shared outside the research team to protect trainee confidentiality.

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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