Effect of Moulage-Based Performance on Violence Against Women Awareness (Moulage-Based)
5 de mayo de 2026 actualizado por: Maltepe University
The Effect of Moulage-Based Silent Performance on Awareness of Violence Against Women: A Randomized Controlled Study Among Nursing Students
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.
Descripción general del estudio
Estado
Inscripción por invitación
Condiciones
Intervención / Tratamiento
Descripción detallada
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.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
70
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
-
-
MAltepe
-
Istanbul, MAltepe, Turquía (Türkiye), 34857
- maltepe University
-
-
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Sí
Descripción
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
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Moulage-Based Silent Performance
Participants in this group were exposed to a moulage-based silent performance involving a female model representing a victim of violence.
The model remained silent and non-interactive throughout the session.
Participants stayed in the room for five minutes and read a narrative letter describing a woman's experience of violence.
After the session, participants completed questionnaires assessing attitudes toward violence against women, empathy levels, and emotional reactivity.
|
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.
|
|
Sin intervención: Neutral Exposure Control
Participants in this group were exposed to a neutral condition involving a female model without moulage makeup.
The model remained silent and non-interactive.
Participants read the same narrative letter describing a woman's experience of violence and then completed the same outcome measures as the intervention group.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in attitudes toward violence against women
Periodo de tiempo: Pre-intervention and immediately post-intervention (within the same session)
|
Attitudes toward violence against women were assessed using the Violence Against Women Attitude Scale (ISKEBE).
The scale consists of 30 items rated on a 5-point Likert scale.
Higher scores indicate stronger rejection of violence and more positive attitudes toward women.
Changes in scores from pre-intervention to post-intervention were compared between the intervention and control groups.
|
Pre-intervention and immediately post-intervention (within the same session)
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in empathy levels
Periodo de tiempo: Pre-intervention and immediately post-intervention (within the same session)
|
Empathy levels were assessed using the Empathic Tendency Scale developed by Dökmen (1988).
The scale consists of 20 items rated on a 5-point Likert scale, with higher scores indicating greater empathic tendency.
Changes in empathy scores from pre-intervention to post-intervention were compared between the intervention and control groups.
|
Pre-intervention and immediately post-intervention (within the same session)
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
1 de enero de 2026
Finalización primaria (Actual)
12 de febrero de 2026
Finalización del estudio (Estimado)
1 de junio de 2026
Fechas de registro del estudio
Enviado por primera vez
5 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
5 de mayo de 2026
Publicado por primera vez (Actual)
11 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
11 de mayo de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
5 de mayo de 2026
Última verificación
1 de mayo de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- E-74555795-050.01.04-52291
- University Research Project (Otro identificador: Maltepe University)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Descripción del plan IPD
The datasets generated during the current study are not publicly available due to ethical considerations but are available from the corresponding author on reasonable request."
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .