- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07803861
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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:
- 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.
- 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.
- Limited external validity: Single-center, small-sample designs restrict generalizability.
- 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.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Hangzhou, China
- The Second Affiliated Hospital of Zhejiang University School of Medicine
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
theoretical exam
Time Frame: up to 2 weeks
|
The assessment included a theoretical exam (maximum score: 100 points)
|
up to 2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mini-CEX Scores
Time Frame: 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
Time Frame: 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
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2026-0693
- 20230242,20240410 (Other Grant/Funding Number: Teaching reform research and cultivation project of The Second Affiliated Hospital of Zhejiang University School of Med)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.