Menu
Not yet recruiting NCT07098559

Effects of Bystander Model-Based Creative Drama on Empathy and Bullying Intervention in Middle School Students

No phase Interventional Bystander Intervention

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: Creative drama.
Who it may be relevant to
Registry conditions: Bystander Intervention. Basic parameters: 10 years — 14 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 Effects of Bystander Intervention Model-Based Creative Drama Workshops on Bystander Intervention and Empathy in Peer Bullying Among Middle School Students: A Randomized Controlled Trial

Overview

This research is a randomized controlled experimental study. The research aims to evaluate the effectiveness of creative drama workshops based on the bystander intervention model on middle school students' bystander intervention and empathy levels. The research population consists of sixth and seventh grade students. The research sample will consist of at least 42 middle school students, 21 in the intervention group and 21 in the control group. The sample will be selected through randomization. The students in the intervention group will receive 10 sessions of creative drama intervention. The research aims to answer the following questions: Is there a difference between the intervention group and the control group in terms of bystander intervention levels? Is there a difference between the intervention group and the control group in terms of empathy levels toward the victim of peer bullying?

Detailed description

Adolescence is a crucial period during which individuals undergo significant physical, mental, and social changes, and the process of identity development begins. The transition to middle school during this period leads to increased interaction with peer groups and an increased likelihood of encountering behaviors such as bullying. Bullying, a form of aggression characterized by intent to harm, repetition, and a power imbalance, is a common occurrence in schools. According to a 2023 report by the United Nations Educational, Scientific, and Cultural Organization (UNESCO), one in three students worldwide is bullied, while in Turkey, rates range from 15.9% to 34.9%. Bullying negatively impacts children's physical, mental, and social development, and these effects can extend into adulthood. During bullying, students may assume various roles, including bully, victim, bully-victim, and bystander. Bystander intervention is particularly critical for preventing bullying. However, research shows that a large portion of bystanders remain passive. However, intervening bystanders have the potential to quickly stop bullying. One effective strategy for preventing bullying is school-based, multifaceted intervention programs. The school nurse plays a crucial role in this process, providing guidance both in identifying bullying and in providing intervention. Empathy is a key determinant in bystander intervention. Individuals with high empathy are more likely to take on an advocacy role. In this context, creative drama can increase students' sensitivity to bullying by fostering empathy. Through creative drama, students can experience the effects of bullying and discuss solutions. Drama helps students express their feelings and develop problem-solving and communication skills. The Bystander Intervention Model defines five stages individuals must go through to help a situation: recognizing the incident, interpreting it as urgent, assuming responsibility, knowing how to help, and intervening. Individual attitudes and environmental factors play important roles in this process. In this context, this study aims to evaluate the effectiveness of creative drama workshops based on the bystander intervention model in increasing middle school students' bystander intervention levels and empathy skills in bullying. The study will be conducted with 6th and 7th grade students and will utilize a randomized controlled experimental design. The sample will consist of 42 students, who will be randomly assigned to an intervention group of 21 and a control group of 21. The experimental group will participate in creative drama workshops based on an audience intervention model, while the control group will not receive any intervention.

Interventions

  • Behavioral Creative drama
    This intervention is unique in its integration of the Bystander Intervention Model with creative drama techniques to enhance empathy, self-efficacy, and active intervention behaviors among middle school students witnessing peer bullying. Unlike traditional anti-bullying programs that rely on lectures or cognitive-based approaches, this study uses experiential learning and role-playing scenarios to simulate real-life bullying situations and encourage emotional engagement and behavioral change.

Primary outcome measures

  • Bystander Intervention Scale in Bullying [Time frame: 3 months]
Secondary outcome measures (1)
  • Empathy Scale for Peer Bullying Victims [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Being in 6th or 7th grade,
  • Having parental consent, and
  • Voluntary participation in the study

Exclusion criteria

  • Difficulty in reading and writing Turkish, and
  • Having a physical/mental disability or illness

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
Single blind
Primary purpose
Prevention

Study locations

Turkey (Türkiye) · 1 center
  • Gazi University — Ankara

Identifiers

NCT: NCT07098559 · E-77082166-302.08.01-1265651

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗