Substance Abuse Clinical Trial
Official title:
An Evidence-based Approach for Bullying Prevention
NCT number | NCT03205059 |
Other study ID # | R44HD074319-02 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | June 1, 2017 |
Est. completion date | May 2020 |
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.
Status | Recruiting |
Enrollment | 3000 |
Est. completion date | May 2020 |
Est. primary completion date | May 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 11 Years to 14 Years |
Eligibility |
Inclusion Criteria: - Middle school aged-youth Exclusion Criteria: - Significant cognitive impairment or severe learning disabilities, as screened by field staff at participating sites |
Country | Name | City | State |
---|---|---|---|
United States | National Health Promotion Associates | White Plains | New York |
Lead Sponsor | Collaborator |
---|---|
National Health Promotion Associates, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in bullying/cyberbullying perpetration in the past two years | 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. | Post-test (within 2 weeks of completing final session/module of the intervention), 12-month follow-up, 24-month follow-up |
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