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临床试验/NCT07372456
NCT07372456已完成不适用

The Effect of Nurse-Led Social Emotional Learning Program on Adolescents' Bullying, Victimization, and Bystander Behaviors

Marmara University1 个研究点 分布在 1 个国家目标入组 210 人开始时间: 2025年10月3日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
210
试验地点
1
主要终点
Bullying and Cyberbullying Scale for Adolescents

研究概览

简要总结

This randomized controlled trial will evaluate the effect of a nurse-led social emotional learning (SEL) program on bullying, victimization, and bystander behaviors among adolescents. The study will be conducted in two public middle schools in Istanbul, Türkiye, with students in grades 6-8. Participants in the intervention group will receive structured SEL sessions designed to enhance emotional regulation, empathy, and problem-solving skills, while the control group will continue with routine education. Outcomes will be measured using validated scales at baseline, three months, and six months after the intervention.

详细描述

School violence is observed at all levels of education, but it is particularly prominent during middle school, which coincides with early adolescence. While violence tends to increase in primary school and decrease in higher grades of high school, no significant differences are observed between grade levels in middle school. Bullying has multiple negative consequences: for perpetrators, it is associated with suicide, weapon carrying, substance use disorders, and a tendency toward violence and criminal behavior in adulthood; for victims, it is linked to low self-esteem, anxiety disorders, and suicide. Due to these multifaceted negative effects, bullying prevention programs must be implemented as public health interventions. This study aims to evaluate the effect of a nurse-led, social emotional learning (SEL)-based education program on bullying, victimization, and bystander behaviors among adolescents attending grades 6, 7, and 8 in middle schools. Unlike many previous studies, this program not only seeks to reduce bullying and victimization but also aims to enhance bystander intervention. Furthermore, the intervention will be uniquely delivered by a nurse with a focus on fostering social emotional skills.This randomized controlled trial will be conducted between October 2025 and June 2026 in two public middle schools located in the Ümraniye district of Istanbul, Türkiye. The study will follow a pre-test, post-test, and follow-up test design with intervention and control groups. Randomization will be applied to ensure comparability, and participants with similar pre-test characteristics will be assigned to either group. The intervention group will receive the SEL-based training program, while the control group will continue with routine education. Post-tests will be conducted three months after the intervention, and follow-up assessments will be carried out at six months. Data will be collected in classrooms through face-to-face self-report surveys. Instruments include the Personal Information Form, Bullying Victimization Self-Efficacy Scale, Bullying and Cyberbullying Scale for Adolescents, Bystander Intervention in Bullying Scale, and Social Emotional Learning Skills Scale.Data entry will be performed electronically, and statistical analyses will be conducted using Jamovi. Tests appropriate for normal distribution will be used. A significance level of p < 0.05 will be considered statistically significant.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
11 Years 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Students enrolled in 6th, 7th, or 8th grade during the study period
  • Students whose parents/legal guardians provide consent for participation
  • Students who volunteer to participate in the study
  • Students without communication barriers

排除标准

  • Students who provide incomplete data in the pre-test, post-test, or follow-up assessments
  • Students who do not fully participate in the intervention program
  • Students with insufficient cognitive level to complete the study requirements

研究组 & 干预措施

Control Group

No Intervention

Students in this group will continue their routine school curriculum without receiving the SEL-based program.

结局指标

主要结局

Bullying and Cyberbullying Scale for Adolescents

时间窗: Baseline (pre-test), 3 months (post-test), 6 months (follow-up)

The Bullying and Cyberbullying Scale for Adolescents (BCS-A) was originally developed by Thomas et al. (2019) and adapted into Turkish by Özbey and Başdaş (2020). The scale consists of two parallel forms measuring bullying and victimization experiences of adolescents during the past three months. Each form includes four subscales: physical, verbal, relational, and cyber. The scale has 26 items in total. Subscale scores are calculated by dividing the sum of the items by the number of items in that subscale. Reported Cronbach's alpha values for the Turkish version range between 0.606-0.806 for the victimization subscale and 0.616-0.815 for the bullying subscale.

Bystander Intervention in Bullying Scale

时间窗: Baseline (pre-test), 3 months (post-test), 6 months (follow-up)

The scale was originally developed by Nickerson et al. (2014) to assess the level of bystander intervention in bullying situations. The Turkish adaptation was conducted by Demirbaş and Öztemel (2019). It consists of 16 items rated on a five-point Likert scale, covering five subdimensions: Noticing the Event, Interpreting the Event as Urgent, Accepting Responsibility to Help, Deciding How to Intervene, and Implementing the Decision to Intervene. Total scores range from 16 to 80, with higher scores indicating a greater likelihood of bystander intervention. Reported internal consistency (Cronbach's alpha) was 0.88 for the overall scale, 0.60 for Noticing the Event, 0.78 for Interpreting as Urgent, 0.67 for Accepting Responsibility, 0.75 for Deciding How to Intervene, and 0.78 for Implementing the Decision.

次要结局

  • Bullying Victimization Self-Efficacy Scale(Baseline (pre-test), 3 months (post-test), 6 months (follow-up))
  • Social Emotional Learning Skills Scale(Baseline (pre-test), 3 months (post-test), 6 months (follow-up))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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