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Clinical Trials/KCT0012367
KCT0012367Active, not recruitingNot Applicable

Development and Effectiveness of a Simulation-Based Educational Program to Enhance Emergency Nurses’ De-escalation Competency in Aggressive Situations

Konyang University0 sites32 target enrollmentStarted: June 15, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
32

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Primary Purpose
Health Services Research, Intervention Model : Parallel, Blinding/Masking : Open, Allocation : RCT

Eligibility Criteria

Ages
No Limit to No Limit (—)
Sex
All

Inclusion Criteria

  • •Nurses currently working in the emergency department of a general hospital or higher-level medical institution
  • •Nurses with at least 6 months of emergency department work experience
  • •Individuals who understand the purpose of the study and voluntarily consent to participate

Exclusion Criteria

  • •Nurses with less than 6 months of emergency department work experience
  • •Nurses who have completed similar de-escalation or violence-response simulation training within the previous 6 months

Arms & Interventions

Behavioral : The experimental group will receive a simulation-based educational program designed to enhance de-escalation competency in aggressive situations in the emergency department. The program consists of four sessions totaling 240 minutes, and each session includes didactic education, simulation practice, and debriefing. Session 1 covers early recognition of potential aggression, maintenance of a safe distance, designation of a single communicator, verbal and nonverbal de-escalation principles, boundary setting, criteria for transition to safety measures, and requesting team support. Session 2 focuses on preventive de-escalation for a patient expressing initial dissatisfaction because of a prolonged emergency department waiting time. Session 3 focuses on responding to an emotionally escalated caregiver by acknowledging emotions, setting boundaries, offering limited choices, and determining whether a transition to safety measures is required. Session 4 focuses on a patient experiencing anxiety and agitation while waiting after examination and treatment and includes anxiety reduction, explanation of the situation, reassessment, reduction of environmental stimuli, provision of choices, and determination of the need for safety measures. The simulation will be conducted in small groups, with participants alternating between performer and observer roles. Each simulation will be followed by structured debriefing using the Description–Analysis–Application format. The control group will not receive any separate de-escalation education or simulation-based program during the study period.

Intervention: Behavioral : The experimental group will receive a simulation-based educational program designed to enhance de-escalation competency in aggressive situations in the emergency department. The program consists of four sessions totaling 240 minutes, and each session includes didactic education, simulation practice, and debriefing. Session 1 covers early recognition of potential aggression, maintenance of a safe distance, designation of a single communicator, verbal and nonverbal de-escalation principles, boundary setting, criteria for transition to safety measures, and requesting team support. Session 2 focuses on preventive de-escalation for a patient expressing initial dissatisfaction because of a prolonged emergency department waiting time. Session 3 focuses on responding to an emotionally escalated caregiver by acknowledging emotions, setting boundaries, offering limited choices, and determining whether a transition to safety measures is required. Session 4 focuses on a patient experiencing anxiety and agitation while waiting after examination and treatment and includes anxiety reduction, explanation of the situation, reassessment, reduction of environmental stimuli, provision of choices, and determination of the need for safety measures. The simulation will be conducted in small groups, with participants alternating between performer and observer roles. Each simulation will be followed by structured debriefing using the Description–Analysis–Application format. The control group will not receive any separate de-escalation education or simulation-based program during the study period.

Investigators

Sponsor
Konyang University

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