150 Participants Needed

BullyDown Program for Bullying Prevention

Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Center for Innovative Public Health Research

Trial Summary

What is the purpose of this trial?

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.

Eligibility Criteria

This trial is for English-speaking 7th or 8th graders who have their own cell phone and home internet. They must be able to provide informed assent. It's not for those who can't read the screener, know someone else in the trial, or don't have an unlimited text messaging plan.

Inclusion Criteria

You are in the seventh or eighth grade of schooling.
English speaking
You have provided your informed consent to participate in the study.
See 2 more

Exclusion Criteria

Unable to read the screener
Know someone else in the RCT
I do not have an unlimited text messaging plan.

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intervention

Participants receive the BullyDown text messaging-based bullying prevention program

8 weeks

Follow-up

Participants are monitored for changes in behavior and program effectiveness

3 months

Treatment Details

Interventions

  • BullyDown
Trial Overview BullyDown is a bullying prevention program delivered via text messages to middle school students. The study compares BullyDown with an attention-matched control group to see which is more effective at preventing bullying.
Participant Groups
2Treatment groups
Experimental Treatment
Placebo Group
Group I: BullyDown interventionExperimental Treatment1 Intervention
Group II: Healthy lifestyle controlPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Center for Innovative Public Health Research

Lead Sponsor

Trials
11
Recruited
8,100+

University of North Carolina, Chapel Hill

Collaborator

Trials
1,588
Recruited
4,364,000+
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