The Application of Intermittent Training in Clinical Skills Simulation Training

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorGeneral Hospital of Ningxia Medical University

About this trial

This study aims to investigate medical students' mastery of advanced life support skills when using scenario-based simulation combined with intermittent training, compared to traditional teaching methods.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Medical students studying in the Department of Anesthesiology

The initial training for "Advanced Life Support Scenario Simulation Instruction" required by this study has been successfully completed, and the corresponding pre-test assessment has been passed.

Voluntarily participate in this study and sign a written informed consent form, committing to adhere to the entire schedule of the research plan.

During the research period, do not participate in any other training that conflicts with this experiment.

Disqualifiers

Individuals who have previously obtained an Advanced Cardiac Life Support (ACLS) provider certificate issued by the American Heart Association (AHA) or an equivalent organization, and whose certificate remains valid.

Individuals who have participated in any form of Advanced Cardiac Life Support (ACLS) or Advanced CPR scenario simulation training courses within the past three months.

Previously participated as a subject in educational interventions comparing "spaced learning versus traditional learning."

Individuals who, for any reason, fail to complete all instructional components during the initial training phase or whose pre-test data is missing.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Interval retraining

    Other intervention

    Through basic skills training and testing, confirm that all trainees have mastered the steps of adult external cardiopulmonary resuscitation (CPR), tracheal intubation procedures, and the operational steps of automated external defibrillators (AEDs). And validated students' mastery of ECG interpretation for cardiac arrest and arrhythmias, along with pharmacology knowledge of cardiovascular emergency medications through assessment questions. The interval retraining group underwent fixed-interval repeated training, performing the same 20-minute tasks daily on days 2, 4, and 6.

  • Non-interval retraining

    Other intervention

    Through basic skills training and testing, confirm that all trainees have mastered the steps of adult external cardiopulmonary resuscitation (CPR), tracheal intubation procedures, and the operational steps of automated external defibrillators (AEDs). And validated students' mastery of ECG interpretation for cardiac arrest and arrhythmias, along with pharmacology knowledge of cardiovascular emergency medications through assessment questions. The non-interval retraining group will not engage in interval training during the following week.

Treatment groups

48 Participants
are divided into 2 treatment groups
Group A: Interval Training GroupExperimental treatment 1 intervention
Group B: Non-interval training groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Advanced Life Support Skills Assessment

Performance Scoring for Cardiopulmonary Resuscitation, Defibrillation, and Tracheal Intubation

Time frame
The seventh day after the unified training
2

Theoretical Knowledge of Advanced Life Support

Interpretation of electrocardiograms related to cardiac arrest, arrhythmias, and other conditions; pharmacological knowledge of emergency medications for the cardiovascular system.

Time frame
The seventh day after the unified training

Secondary outcomes

1

Total Duration of Scenario Simulation

Total time required to resuscitate the patient in the simulated case

Time frame
The seventh day after the unified training
2

Scenario-Based Simulation Training Participant Behavior Checklist

Conduct standardized behavioral verification of trainees participating in scenario-based simulation training based on teaching cases.

Time frame
The seventh day after the unified training
3

Student Satisfaction Survey Form

Participant satisfaction with the training content and outcomes

Time frame
The seventh day after the unified training

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: