MedTrace Logo

Evaluation of Green Dot a Primary Prevention Intervention

NCT01878097 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 89707

Last updated 2019-03-15

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate the statewide application of Green Dot among high schools students. We hypothesize that students in high schools with Green Dot will over time report lower rates of sexual violence (SV) compared with students in comparable high schools randomized not to have Green Dot. This reduction in sexual violence will be mediated through a reduction in social norms supporting sexual violence (measured with violence acceptance scales) and an increase in bystander behaviors.

Conditions

  • Sex Offenses

Interventions

BEHAVIORAL

Green Dot Bystander Intevention

Intervention allocated at the school level

BEHAVIORAL

Control

Awareness Education

Sponsors & Collaborators

  • University of Kentucky

    lead OTHER

Principal Investigators

  • Ann L. Coker, PhD · University of Kentucky

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2014-05-31
Completion
2014-05-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01878097 on ClinicalTrials.gov