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ConnectEd: A Randomized Controlled Trial Connecting Through Educational Training

NCT02786472 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3178

Last updated 2020-02-24

No results posted yet for this study

Summary

The purpose of this randomized intervention pilot is to evaluate the relative efficacy of bystander training elements (delivery mode and integration of substance abuse prevention) among cohorts of incoming undergraduates at the University of Kentucky, a nationally recognized leader in addressing sexual violence through bystander intervention programming. Consenting students will be randomized to one of the following training conditions:

1. In-person Green Dot Intensive Bystander-based Sexual Violence Prevention Training (GreenDot);
2. In-person Green Dot Intensive Bystander Training combined with Substance Abuse Prevention Training;
3. Online Bystander-based Sexual Violence Prevention Training (Haven), and;
4. Online Substance Abuse Training (AlcoholEdu).

Conditions

  • Sexual Violence

Interventions

BEHAVIORAL

Online Bystander Training

Large groups of 120-150 students will complete Haven training via computer; training lasts duration of the online program.

BEHAVIORAL

Online Substance Abuse Training

Large groups of 120-150 students will complete EverFi training via computer; training lasts duration of the online program.

BEHAVIORAL

In-Person Bystander Training

In-person training of large groups of 120-150 students; training lasts 3-4 hours

BEHAVIORAL

In-Person Combination Training

In-person training of large groups of 120-150 students; training lasts 3-4 hours

Sponsors & Collaborators

  • Centers for Disease Control and Prevention

    collaborator FED

  • Heather Bush

    lead OTHER

Principal Investigators

  • Heather M Bush, PhD · University of Kentucky

  • Ann L Coker, MPH, PhD · University of Kentucky

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
17 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2019-12-31
Completion
2019-12-31

Countries

  • United States

Study Locations

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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 NCT02786472 on ClinicalTrials.gov