School Program for Resilience and Bullying Prevention
2026年6月29日 更新者：Osman Kuçukkelepce, MD、Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
School-Based Intervention to Enhance Psychological Resilience and Bullying Awareness Among High School Students: A Mixed-Methods Study
This study evaluated whether a school-based psychoeducational program could improve psychological resilience and reduce bullying victimization among high school students in Hatay, Türkiye, following the 2023 earthquake.
The intervention consisted of a 10-week psychological resilience program followed by a 5-week peer bullying awareness program delivered in weekly group sessions.
A single-group pretest-posttest mixed-methods design was used.
Psychological resilience and bullying victimization were assessed before the intervention and three months after program completion using validated self-report scales.
Qualitative data were also collected to explore students' experiences and perceived benefits of the program.
調査の概要
状態
完了
詳細な説明
Adolescents living in disaster-affected regions may experience increased psychological distress, reduced resilience, and greater vulnerability to peer bullying. School-based psychoeducational interventions may strengthen coping skills, improve emotional regulation, and promote healthier peer relationships.
This study was conducted in Hatay, Türkiye, following the February 2023 earthquakes to examine changes in psychological resilience and bullying victimization after participation in a structured psychoeducational intervention.
The study used a single-group pretest-posttest mixed-methods design. High school students participated in a 15-week intervention consisting of two sequential components. The first component was a 10-week psychological resilience program designed to improve self-awareness, emotional regulation, coping skills, self-efficacy, goal setting, and social support. The second component was a 5-week peer bullying awareness program developed by the Ministry of National Education with educational support from UNICEF, focusing on recognizing bullying, empathy, bystander intervention, and prevention strategies.
Quantitative outcomes were measured using the Child and Youth Resilience Measure-12 (CYRM-12) and the Child-Adolescent Bullying Scale-9 Short Form (CABS-9). Assessments were performed before the intervention and three months after completion of the program. Qualitative data were collected using open-ended written questions to explore participants' perceptions of the intervention and its effects.
The primary objective was to evaluate changes in psychological resilience and bullying victimization following participation in the program. Secondary objectives included exploring students' experiences of the intervention and identifying perceived changes in personal development, peer relationships, and school climate.
研究の種類
介入
入学 (実際)
101
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Hatay、トルコ（Türkiye）
- Antakya High School
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 子
- 大人
健康ボランティアの受け入れ
はい
説明
**Inclusion Criteria:**
- Students enrolled in grades 9, 10, or 11 at the participating high school in Hatay, Türkiye.
- Aged between 14 and 18 years.
- Able to understand and complete the study questionnaires.
- Willing to participate in the school-based intervention.
- Written informed consent obtained from parents or legal guardians, and assent obtained from the student where applicable.
**Exclusion Criteria:**
- Students who did not provide informed consent or whose parents/legal guardians did not provide consent.
- Students who were absent from the majority of intervention sessions.
- Students who did not complete both the baseline and follow-up assessments.
- Students who withdrew from the study at any time during the intervention period.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：防止
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：Intervention Group
Participants in this single-arm study received a sequential 15-week school-based behavioral intervention.
The intervention consisted of a 10-week Psychological Resilience Program followed immediately by a 5-week Peer Bullying Awareness Program.
Weekly group sessions focused on developing emotional regulation, coping skills, resilience, communication, social support, empathy, bullying awareness, bystander intervention, conflict resolution, and bullying prevention.
All participants received both intervention components in the same order, and outcomes were assessed before the intervention and three months after program completion.
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The Psychological Resilience Program was a structured, school-based psychoeducational intervention delivered in weekly group sessions over 10 consecutive weeks.
The program was designed to strengthen adolescents' psychological resilience following the 2023 earthquakes in Türkiye.
The curriculum included activities aimed at improving self-awareness, emotional awareness and regulation, stress management, problem-solving, coping strategies, communication skills, self-efficacy, goal setting, optimism, social support, and adaptive responses to challenging life events.
Sessions were conducted using interactive methods, including group discussions, experiential activities, role-playing, reflection exercises, and practical skill-building tasks.
The intervention was delivered by trained professionals according to a standardized program protocol.
The Peer Bullying Awareness Program was delivered immediately after completion of the resilience program and consisted of five weekly school-based group sessions.
The program was developed by the Turkish Ministry of National Education with educational support from UNICEF and was designed to increase awareness of peer bullying and promote healthy peer relationships.
Session topics included the definition and types of bullying, recognition of bullying behaviors, empathy development, emotional awareness, effective communication, bystander responsibilities, conflict resolution, reporting mechanisms, and strategies for preventing bullying in school settings.
Interactive discussions, scenario-based learning, group activities, and reflective exercises were used to encourage active participation and application of the concepts in everyday school life.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Psychological Resilience
時間枠：Baseline and 3 months after completion of the intervention.
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Psychological resilience will be assessed using the Child and Youth Resilience Measure-12 (CYRM-12), a validated self-report instrument that evaluates individual, relational, and contextual resilience resources among adolescents.
The total CYRM-12 score will be used to determine changes in participants' resilience following the intervention.
Higher scores indicate greater psychological resilience and adaptive coping capacity.
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Baseline and 3 months after completion of the intervention.
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Peer Bullying victimization
時間枠：Baseline and 3 months after completion of the intervention.
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Peer bullying victimization will be assessed using the Child-Adolescent Bullying Scale-9 Short Form (CABS-9), a validated self-report instrument that measures the frequency and severity of bullying experiences among adolescents.
Total CABS-9 scores will be compared before and after the intervention to evaluate changes in peer bullying victimization.
Lower scores indicate reduced exposure to peer bullying and improved school social experiences.
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Baseline and 3 months after completion of the intervention.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Participants' Experiences of the Intervention
時間枠：3 months after completion of the intervention.
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Participants' experiences and perceptions of the intervention will be explored using open-ended qualitative questions administered three months after completion of the program.
Responses will be analyzed using thematic content analysis to identify perceived changes in psychological resilience, coping strategies, emotional well-being, peer relationships, bullying awareness, and the overall usefulness of the intervention.
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3 months after completion of the intervention.
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2025年9月10日
一次修了 (実際)
2026年3月15日
研究の完了 (実際)
2026年3月20日
試験登録日
最初に提出
2026年6月29日
QC基準を満たした最初の提出物
2026年6月29日
最初の投稿 (実際)
2026年7月6日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月6日
QC基準を満たした最後の更新が送信されました
2026年6月29日
最終確認日
2026年6月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- 902-01-FR 006
- MEB.TT.2025.029302.01 (その他の識別子：Republic of Türkiye Ministry of National Education (MoNE) veya Turkish Ministry of National Education)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
はい
IPD プランの説明
De-identified individual participant data underlying the results reported in this study will be made available to qualified researchers upon reasonable request to the corresponding author.
Data will be shared after publication of the study, subject to approval of a methodologically sound research proposal and in accordance with institutional ethics requirements and applicable data protection regulations.
The corresponding author will provide the data upon request.
IPD 共有時間枠
De-identified individual participant data and supporting documents will be available beginning 6 months after publication of the study and will remain available for 5 years.
IPD 共有アクセス基準
De-identified individual participant data, the study protocol, statistical analysis plan, and analytic code will be made available to qualified researchers upon reasonable request to the corresponding author.
Requests must include a methodologically sound research proposal and may require approval by the study investigators and the relevant institutional ethics committee.
Data will be shared in accordance with institutional policies, participant confidentiality requirements, and applicable data protection regulations.
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
試験データ・資料
-
研究プロトコル
情報識別子：Study Protocol v1.0情報コメント：The study protocol is available in the shared repository.
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個人参加者データセット
情報識別子：Deidentified IPD v1.0情報コメント：De-identified individual participant data underlying the findings of this study are available through the shared repository. The dataset contains anonymized participant-level data with all direct identifiers removed and is provided for research purposes in accordance with institutional ethics requirements.
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。