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RecruitingNCT07905807SIC-BURN-JAAM2Updated Oct 29, 2026

Early Detection and Kinetics of Sepsis-Induced Coagulopathy in Severe Burn Patients

An observational study in Peer Bullying Intervention, Vodcast and Students, sponsored by Selcuk University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 10 Years to 13 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Selcuk University · Observational

Updated Oct 29, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
128
Ages
10 Years to 13 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the impact of an avatar-supported, teacher-student interactive, vodcast-based peer bullying prevention program-developed for adolescents-on students' ability to identify peer bullying, their experiences with bullying, fighting, and victimization, and their levels of empathy.

Designed as a non-randomized controlled study (quasi-experimental), this research will be conducted between October 2026 and December 2026 with students attending two public middle schools under the Ministry of National Education in the city center of Nevşehir. Based on an analysis using the G*Power (v3.1.9.7) software-with parameters set at an effect size of 0.5, a significance level of 0.05, and a test power of 0.80-the sample size has been determined to be 128 students in total, with 64 students in each of the experimental and control groups. Data will be collected using the "Student Demographic Information Form," the "Peer Bullying Identification Scale (Adolescent Form)," the "Illinois Bullying, Fighting, and Victimization Scale," and the "Empathy Scale for Children," all of which will be prepared by the researcher. During the intervention phase, the experimental group will watch five avatar-supported, teacher-student interactive vodcasts (educational video content), while the control group will receive no intervention. Data analysis will involve the Independent Samples t-test, as well as the Pearson Chi-square and Fisher's Exact tests for categorical data. A Mixed-Design Analysis of Variance (Mixed ANOVA) will be used to compare variables across follow-up time points, and the Bonferroni correction will be applied when comparing main effects. A p-value of \<0.05 will be considered statistically significant; ethical principles will be strictly upheld throughout the study, with a focus on obtaining parental consent and ensuring the voluntary participation of students.

02

Conditions studied

  • Peer Bullying Intervention
  • Vodcast
  • Students

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Keywords

  • Vodcast
  • Peer Bullying
  • Education
  • student
03

In context

Bullying

57 studies on the registry are indexed under Bullying; 9 are open to participants now.

Browse Bullying studies →

Lead sponsor

Selcuk University is the lead sponsor of 258 studies on the registry; 67 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 13 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study group will consist of students enrolled in the specified schools. A medium effect size (Cohen's d = 0.50) was used as a reference for this study. Power analysis was conducted using the G*Power 3.1.9.6 software. The analysis employed an independent samples t-test to examine the difference between two independent groups, based on a two-tailed hypothesis, an effect size of 0.50, a power of 80% (1-β = 0.80), a significance level of 0.05 (α = 0.05), and an allocation ratio of 1:1 between the groups. The calculations indicated that a total sample size of 128 students (64 in the intervention group and 64 in the control group) would be sufficient for the study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Being a student enrolled in the relevant schools
  • Having obtained a parental consent form
  • Possessing the cognitive ability to follow the program (i.e., not being a student in an inclusive/mainstreamed education setting for special needs)

Exclusion criteria

Exclusion Criteria

  • Unwillingness to participate in the study
  • Absence of parental consent
  • Having special educational needs (e.g., visual or hearing impairments, or any health condition that would prevent the completion of questionnaires)
  • Having previously received training on peer bullying

Withdrawal Criteria

  • Missing two or more sessions of the training program
  • Choosing to withdraw from the study after having already begun participation
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
128 participants (estimated)
Target follow-up
5 Weeks
Patient registry
Yes

Groups and cohorts

  • Experimantal Group: Vodcast-Based Peer Bullying Intervention

    Students in the intervention group will participate in a vodcast-based peer bullying prevention program, consisting of a total of five sessions, with one session held per week.

    Behavioral: Vodcast-Based Peer Bullying Intervention

  • Control Group

    Students in the control group will follow the routine procedure; once the post-test data collection is complete, the program designed for the intervention group will be presented in a single-day session for any students who wish to view it.

Interventions

  • BehavioralVodcast-Based Peer Bullying Intervention

    Students in the intervention group will participate in a vodcast-based peer bullying prevention program, consisting of five sessions-one session per week. As part of the program, vodcasts covering a different theme related to peer bullying will be presented each week within the school setting, in a quiet and suitable classroom environment designed to minimize distractions. The sessions will be conducted under the supervision of the researcher, ensuring that all students watch the vodcasts under consistent technical conditions. Each session will last approximately 20 minutes; during the first part, students will watch that week's vodcast, followed by a discussion in which the researcher will pose open-ended questions to encourage students to reflect on the content.

06

What researchers measure

Primary outcomes

  1. Student Information Form

    This form, created by the researchers, will be administered on the first day of the first week-prior to the start of the intervention-taking into account the specific circumstances of the school and the classrooms where the implementation will take place.

    Time frame: First measurement-First week,The first day of the week

  2. Peer Bullying Scale Adolescent Form

    This form will be administered on the first day of the first week-prior to the start of the intervention-taking into account the specific circumstances of the school and the classrooms where the implementation will take place.

    Time frame: First measurement-First week,The first day of the week

  3. Illinois Bullying, Fighting, and Victimization Scale

    This form will be administered on the first day of the first week-prior to the start of the intervention-taking into account the specific circumstances of the school and the classrooms where the implementation will take place.

    Time frame: First measurement-First week,The first day of the week

  4. Empathy Scale for Children Empathy Scale for Children

    This form will be administered on the first day of the first week-prior to the start of the intervention-taking into account the specific circumstances of the school and the classrooms where the implementation will take place.

    Time frame: First measurement-First week,The first day of the week

Secondary outcomes

  1. Peer Bullying Scale Adolescent Form

    This form will be administered on the first day of the fifth week, following the completion of the intervention, while taking into account the specific conditions of the school and the classrooms where the implementation takes place.

    Time frame: Second measurement-Fifth week,The first day of the week

  2. Illinois Bullying, Fighting, and Victimization Scale

    This form will be administered on the first day of the fifth week, following the completion of the intervention, while taking into account the specific conditions of the school and the classrooms where the implementation takes place.

    Time frame: Second measurement-Fifth week,The first day of the week

  3. Empathy Scale for Children

    This form will be administered on the first day of the first week-prior to the start of the intervention-taking into account the specific circumstances of the school and the classrooms where the implementation will take place.

    Time frame: Second measurement-Fifth week,The first day of the week

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2026 (actual). Primary completion is estimated for Dec 2026, 1 month after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 23, 2026
First posted
Oct 29, 2026
StartActual
Oct 24, 2026
Primary completionEst.
Dec 10, 2026
CompletionEst.
Dec 10, 2026
Last update
Oct 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07905807
Lead sponsor
Selcuk University
Responsible party
Sibel Küçükoğlu (Prof, Selcuk University) — Principal investigator
First posted
Oct 29, 2026
Start date
Oct 24, 2026
Primary completion
Dec 10, 2026 (estimated)
Completion
Dec 10, 2026 (estimated)
Last update
Oct 29, 2026

Study contacts

Sibel Küçükoğlu
Contact
s_nadaroglu@hotmail.com
05062848100
Sibel Küçükoğlu
study director · Selcuk University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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