- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06796621
Building Respectful Online Space (BROS): Evaluating a Co-designed Anti-cyberbullying Intervention Among Adolescents
Effectiveness of Co-designed Anti-cyberbullying Intervention [Building Respectful Online Space (BROS)] Among Adolescents: A Feasibility Study
Background: The growing prevalence of cyberbullying throughout the world indicates the importance of anti-cyberbullying interventions, especially for adolescents. While few interventions target cyberbullying, content from different regions may not necessarily apply to local contexts, adolescents' viewpoints were not considered in the past designs, few local RCTs, and unclear sustainability.
Objectives: To evaluate the feasibility, acceptability and preliminarily effects of the co-designed anti-cyberbullying intervention: Building Respectful Online Space (BROS).
Methods: A sample of around 90 aged 12 to 15 will be recruited from secondary schools in Hong Kong. This study will adopt a 2-arm experimental trial. Each class will be randomly assigned equally into the intervention arm (BROS) and control arm (Heathy Diet), and eligible students will be allocated to either arm accordingly. The intervention will be provided in one or 3 days based on the school schedule. Participants will be assessed at baseline, 3 weeks later, and 12-week follow-up assessments. The primary outcome is cyberbullying behaviour of perpetration and victimisation; the secondary outcome includes cyberbullying attitudes, sleep quality, and psychosocial well-being. Feasibility and acceptability will be assessed. And generalised estimating equations analysis will be used to investigate the research objectives.
Potential contributions: The results of this study will provide evidence-based support for using a blended approach to prevent cyberbullying, promote psychosocial well-being, and promote sleep health. This intervention is dedicated to using evidence-to-user-driven ideas to develop culturally sensitive interventions to effectively prevent cyberbullying in the future.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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New Territories, Hong Kong
- The Chinese University of Hong Kong
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students in 1st to 3rd grades in secondary schools
- Students are able to read and understand Chinese
- Students obtained informed consent signed by their parents or legal guardians
Exclusion Criteria:
- Students in grades 4th through 6th who are heavily involved in homework and examination
- Students with severe diseases or co-occurring disorders
- Students' parents/ legal guardians who refuse to sign informed consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Building Respectful Online Space (BROS)
The intervention group participants will receive the BROS intervention across three sessions, depending on the school schedule, presented in a hybrid mode.
The sessions focus on integrating psychoeducation, behavioural-specific cognitions, serious games, music, and reflection, as a means against cyberbullying.
The content includes knowledge related to cyberbullying and online safety, cyberbullying coping skills, relationship skills, emotion management, and empathy towards victims through classroom sessions, short videos, serious games, and online musical therapy.
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Session 1 (40 minutes to 50 minutes): Respectful online relationship (Psychoeducation) using face-to-face approach with 40 minutes to 50 minutes online serious game Session 2 (40 minutes to 50 minutes): Navigating the online world (Psychoeducation) using face-to-face approach with 20 to 30 minutes online music therapy Session 3 (40 minutes to 50 minutes): Behaviour specific cognitions and reflection using face-to-face approach
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Placebo Comparator: Healthy diet education program
For the control group participants, an alternative intervention (a healthy diet education program) with content unrelated to cyberbullying prevention will be given.
The control group participants will receive the alternative intervention across three sessions.
The content is based on recommendations from the Centre for Health Protection, the Government of the Hong Kong Special Administrative Region (CHP, 2024) on healthy eating pyramids, emotional eating, healthy weight management, and nutritional requirements for adolescents.
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Session 1 (40 - 50 minutes): Healthy Diet Pyramid (Psychoeducation) using face-to-face approach Session 2 (40 - 50 minutes): Mindful Eating and Healthy Weight Management (Psychoeducation) using face-to-face approach Session 3 (40 - 50 minutes): Healthy Eating Habits for Life (Psychoeducation)using face-to-face approach
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Cyberbullying behaviour
Time Frame: Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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The Cyberbullying Behaviour Scale (CBBS) consists of E-Victimisation Scale (E-VS) and the E-Bullying Scale (E-BS), is the validated 11-item scale for measuring cyberbullying behaviour.
The scale consist of two domain: 5-item of E-VS and 6-item of E-BS for adolescents with a 7-point Likert scale (Lam & Li, 2013) that measure cyberbullying victimization and perpetration respectively.
The sum score for E-VS range from 5-35, and E-BS from 5-42, and a higher score indicate severity of respective cyberbullying behavior (Lam & Li, 2013).
The Chinese version of CBBS will be used that was translated and validated by our research team.
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Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Cyberbullying attitude
Time Frame: Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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Cyberbullying Attitude Scale (CBAS) is used to identify positive cyberbullying attitude.
The CBAS is a 9-item self-report scale using a 5-point Likert scale (Barlett et al., 2016).
It consists of 5 items for harmful cyberbullying attitudes (HCA), which assess individuals' perceptions of cyberbullying perpetration, and 4 items for general cyberbullying characteristics (GCC).
The range of HCA scores from 5 to 25 and the range of GCC scores from 4 to 20.
A higher score indicates more harmful cyberbullying attitudes.
The Chinese version of CBAS will be used that was translated and validated by our research team.
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Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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Sleep outcomes: Subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, sleep medication, and daytime dysfunction
Time Frame: Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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The Chinese version of Pittsburgh Sleep Quality Index (PSQI) will be used to assess subjective sleep disruption and quality throughout the previous month (Ho et al., 2021).
Subjective sleep quality, sleep latency, duration, habitual sleep efficiency, sleep disruptions, sleep medication, and daytime dysfunction are the seven components that comprise the components of the PSQI.
The range of scores for each item is 0 (no difficulty) to 3 (extreme difficulty).
The total score ranges between 0 and 21.
Poorer quality of sleep is indicated by a higher overall score.
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Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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Mental well-being
Time Frame: Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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The Chinese version of the WHO 5-item Well-Being Index is used to assess participants' mental well-being (Fung et al., 2022).
Each item is rated on a six-point Likert scale, ranging from 0 (at no time) to 5 (always), the total score range from 0 to 25.
A higher score indicates greater mental well-being.
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Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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Life satisfaction
Time Frame: Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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The Chinese version of the Satisfaction With Life Scale (SWLS) (SWLS) is used to assess global cognitive judgments of satisfaction with one's life (Sachs, 2003).It consists of 5 items with a 7-item Likert scale (Pavot & Diener, 1993), ranging from 1 (strongly disagree) to 7 (strongly agree) .
The total score ranges from 7 to 35, with a higher score represent grater social well-being.
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Baseline, pre-intervention, immediately after the intervention, and 3 months follow-up assessment after intervention
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CUHK-2025-YL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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