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Clinical Trials/NCT06017050
NCT06017050
Completed
N/A

Developing a Bullying Prevention Program That Transcends Physical Boundaries

Center for Innovative Public Health Research2 sites in 1 country138 target enrollmentAugust 15, 2023
ConditionsBullying

Overview

Phase
N/A
Intervention
Not specified
Conditions
Bullying
Sponsor
Center for Innovative Public Health Research
Enrollment
138
Locations
2
Primary Endpoint
Feasibility: Recruitment Rate
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

Given the limited impact of existing school-based interventions and the time associated with implementing them during school time, more efficient and effective intervention methods are needed. Programs that can be delivered to middle school youth irrespective of whether they are attending school physically or virtually may be especially relevant as school boundaries become more fluid. BullyDown addresses this critical need by providing a scalable program that could be quickly and cost-effectively disseminated nationally.

Registry
clinicaltrials.gov
Start Date
August 15, 2023
End Date
June 3, 2024
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Center for Innovative Public Health Research
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Feasibility: Recruitment Rate

Time Frame: Recruitment period

If at least 75% of eligible participants assent to participate, this will be supportive of a hypothesis of feasibility. Note that a youth could assent and not be randomized if they did not complete the baseline survey.

Acceptability of the Intervention

Time Frame: Intervention end, 9 weeks after program enrollment

Youth were asked: "How likely are you to recommend BullyDown to other people your age?" Answers were collected on a 5-point Likert scale. The response option ranged from 1-5, with higher values reflecting greater acceptability. An average score of 4 or higher was deemed supportive of program acceptability.

Feasibility: Retention at 3-month Follow-up

Time Frame: 21 weeks post-randomization, 3 months after the 9-week program ended

A retention rate of 80% or higher was deemed to be supportive of a hypothesis of feasibility

Secondary Outcomes

  • Feasibility: Retention Rate at Program End(9 weeks post-randomization)

Study Sites (2)

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