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Enrolling by invitation NCT07578350

Effect of Moulage-Based Performance on Violence Against Women Awareness

No phase Interventional Violence Against Women (VAW) Domestic Violence EMPATHY İN NURSİNG Awareness Training

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Moulage-Based Silent Performance.
Who it may be relevant to
Registry conditions: Violence Against Women (VAW), Domestic Violence, EMPATHY İN NURSİNG, Awareness Training. Basic parameters: 18 years — 20 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Moulage-Based Silent Performance on Awareness of Violence Against Women: A Randomized Controlled Study Among Nursing Students

Overview

This randomized controlled study aimed to evaluate the effect of a moulage-based silent performance on awareness of violence against women, empathy levels, and emotional reactivity among first-year nursing students. Participants were randomly assigned to intervention and control groups. The intervention group was exposed to a moulage makeup-based silent performance representing a victim of violence, while the control group was exposed to a neutral condition. Outcomes were measured using validated scales before and after the intervention.

Detailed description

This study was conducted using a pretest-posttest randomized controlled experimental design among first-year nursing students. Participants were randomly assigned to either the intervention or control group. The intervention group was exposed to a moulage-based silent performance involving a female model representing a victim of violence. Participants remained in the room for five minutes and read a narrative letter describing a woman's experience of violence.

The control group was exposed to the same environment but with a neutral, non-moulage model and read the same letter. Outcomes included attitudes toward violence against women, empathy levels, and emotional reactivity, measured using validated instruments.

The study was conducted in two separate classrooms simultaneously to prevent contamination between groups.

Interventions

  • Behavioral Moulage-Based Silent Performance
    Participants were exposed to a moulage-based silent performance involving a female model representing a victim of violence. The model remained silent and non-interactive. Participants stayed in the room for five minutes and read a narrative letter describing a woman's experience of violence.

Primary outcome measures

  • Change in attitudes toward violence against women [Time frame: Pre-intervention and immediately post-intervention (within the same session)]
Secondary outcome measures (1)
  • Change in empathy levels [Time frame: Pre-intervention and immediately post-intervention (within the same session)]

Eligibility criteria

Inclusion criteria

First-year nursing students Aged between 18 and 35 years Able to read and understand Turkish Voluntary participation with written informed consent

Exclusion criteria

Self-reported psychiatric diagnosis Presence of severe visual or hearing impairments Refusal to participate or withdrawal at any stage of the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Turkey (Türkiye) · 1 center
  • MAltepe University — Istanbul

Identifiers

NCT: NCT07578350 · E-74555795-050.01.04-52291 · University Research Project

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗