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Clinical Trials/NCT03205059
NCT03205059
Unknown
N/A

An Evidence-based Approach for Bullying Prevention

National Health Promotion Associates, Inc.1 site in 1 country3,000 target enrollmentJune 1, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Bullying
Sponsor
National Health Promotion Associates, Inc.
Enrollment
3000
Locations
1
Primary Endpoint
Change in bullying/cyberbullying perpetration in the past two years
Last Updated
7 years ago

Overview

Brief Summary

This Phase II SBIR project is designed to address the critical public health problem of bullying and cyberbullying among middle school age youth. The project involves developing and testing bullying and cyberbullying prevention materials, including interactive classroom sessions and corresponding serious games, based on the evidence-based substance abuse prevention approach called Life Skills Training. The product has the potential to fill a gap in the intervention tools currently available to schools that can be widely disseminated throughout the country using existing marketing and dissemination channels and decrease the adverse consequences of bullying and cyberbullying as well as substance abuse.

Registry
clinicaltrials.gov
Start Date
June 1, 2017
End Date
May 2020
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christopher Williams

Senior Vice President

National Health Promotion Associates, Inc.

Eligibility Criteria

Inclusion Criteria

  • Middle school aged-youth

Exclusion Criteria

  • Significant cognitive impairment or severe learning disabilities, as screened by field staff at participating sites

Outcomes

Primary Outcomes

Change in bullying/cyberbullying perpetration in the past two years

Time Frame: Post-test (within 2 weeks of completing final session/module of the intervention), 12-month follow-up, 24-month follow-up

The investigators will assess (via questionnaire) key study variables regarding bullying and cyberbullying and hypothesized risk and protective factors. These outcomes will be examined and compared in both the intervention group and the active comparator group at a post-test assessment and 12-month and 24-month follow-up assessments.

Study Sites (1)

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