Cyberbullying, Empathy, and Storytelling in Adolescents (NCT06508736) | Clinical Trial Compass
CompletedNot Applicable
Cyberbullying, Empathy, and Storytelling in Adolescents
Turkey (Türkiye)71 participantsStarted 2024-09-01
Plain-language summary
This randomized controlled experimental study examined the effect of a storytelling intervention on cyberbullying and empathy levels in adolescents. The study population consisted of 5th- and 6th-grade middle school students, and the sample included students involved in cyberbullying. Participants were allocated to intervention and control groups using stratified randomization by gender. The intervention group received four storytelling sessions, whereas no intervention was delivered to the control group during the study period. Outcomes were assessed at baseline, post-test, 3-month follow-up, and 6-month follow-up. After the study was completed, the control group was provided with cyberbullying education. The study investigated whether the intervention led to differences between groups in cyberbullying and empathy levels.
Who can participate
Age range
10 Years – 13 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Family approval
* Volunteering to participate in the study.
* Being a 5th and 6th grade student
* Engaging in cyberbullying behavior
Exclusion Criteria:
* Having a diagnosis of any mental illness
* Having at least one of vision, speech and hearing disabilities
* Foreign nationality
* Being a 7th and 8th grade student
* Not engaging in cyberbullying behavior
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.