MedTrace Logo

Impact of Moulage-Based Simulation on Nursing Students' Recognition of Physical Violence

NCT06982014 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2025-05-21

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the effectiveness of moulage-based simulation training in improving nursing students' ability to recognize physical violence in women. The main questions it aims to answer are:

Does moulage-based simulation improve nursing students' ability to recognize signs of physical violence in women compared to traditional training methods? How does the simulation affect nursing students' attitudes and knowledge about gender-based violence? Researchers will compare an experimental group, which will participate in moulage-based simulation training, to a control group that will receive a standard educational video on the topic of gender-based violence. This comparison will assess whether the simulation method provides better outcomes in terms of recognizing violence and improving students' attitudes.

Participants will:

Engage in a clinical simulation involving standardized patients showing signs of physical violence.

Complete pre- and post-training assessments, including attitude surveys and knowledge tests.

Reflect on their learning experience through post-intervention evaluations.

Conditions

  • Nursing Education

Interventions

BEHAVIORAL

cilinical simulation

he experimental group will interact with standardized patients (using moulage techniques) who exhibit signs of physical violence. This approach provides a realistic environment for students to assess the physical manifestations of violence and practice their recognition skills in a controlled, yet lifelike, setting.

OTHER

Educational Video Viewing

The control group will watch a film titled "Gözlerimde Al" (translated as "Take My Eyes"), which addresses the issue of gender-based violence. The film aims to provide insights into the emotional and physical effects of violence against women and encourages reflection on how to recognize such violence in real-life scenarios.

Sponsors & Collaborators

  • Kocaeli Sağlık ve Teknoloji Üniversitesi

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-18
Primary Completion
2025-03-21
Completion
2025-03-21

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06982014 on ClinicalTrials.gov