We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Multi-College Bystander Efficacy Evaluation

This study is enrolling participants by invitation only.
Sponsor:
ClinicalTrials.gov Identifier:
NCT02659423
First Posted: January 20, 2016
Last Update Posted: January 26, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Centers for Disease Control and Prevention
Information provided by (Responsible Party):
Ann Coker, University of Kentucky
  Purpose

Bystander interventions, recognized as promising violence prevention strategies, are unique in their engagement of all community members to 1) recognize situations that may become violent and 2) learn to safely and effectively intervene to reduce violence risk. Based on their promise, the Campus Sexual Violence Elimination Act (SaVE) now requires all publicly-funded colleges to provide bystander intervention. With SaVE's policy intervention requiring bystander interventions, a "natural experiment" has arisen to determine the relative efficacy of students' bystander training across multiple colleges. Investigators propose a quasi-experimental design (using fractional factorials) to evaluate the relative efficacy of three bystander interventions to reduce violence in college communities. Green Dot will be one of three bystander interventions evaluated. A recent rigorous evaluation has found that Green Dot is associated with a 20-40% reduction in VAW in college and high school settings.

In aim 1, investigators will compare the relative efficacy of bystander interventions to a) increase bystander efficacy and behaviors, b) reduce violence acceptance, c) reduce interpersonal violence victimization and perpetration, and d) increase program cost effectiveness. The three main bystander groups compared will be: exclusively online training, Green Dot (speeches and intensive bystander training), and other skills-based bystander training. Program efficacy data will be obtained from student surveys, campus crime statistics, and surveys with college staff and administrators responsible for selecting and implementing bystander interventions.

In aim 2, investigators seek to grow communities of VAW prevention researchers. Researcher communities will form through researchers' engagement with college recruitment, survey design, data collection and analyses. Specifically investigators will determine the efficacy of this program to increase VAW prevention research productivity defined as a) increasing research skills and b) increasing research communications measured as manuscript submissions, presentations, and publications.

This natural experiment will generate new understanding into efficacy of how bystander programs work. This natural experiment will also provide the VAW research community an opportunity to increase our skill-sets and share our experiences with and help grow the next generation of VAW prevention researchers.


Condition Intervention
Sexual Violence Behavioral: BIC 1 Behavioral: BIC 2 Behavioral: BIC 3

Study Type: Observational
Study Design: Observational Model: Other
Time Perspective: Prospective
Official Title: Growing Researcher and College Communities Supporting Violence Prevention Research

Further study details as provided by Ann Coker, University of Kentucky:

Primary Outcome Measures:
  • Interpersonal Violence Victimization and Perpetration at the college level using AAU measures of sexual violence, dating violence, sexual harassment and stalking [ Time Frame: Up to 60 months ]
    Interpersonal Violence defined as sexual violence, partner violence, stalking and sexual harassment


Secondary Outcome Measures:
  • Bystander behavior measures at the college level based on of Banyard, Plante & Monynihan bystanding scale [ Time Frame: Up to 60 months ]
    Bystander intentions, perceived efficacy, behaviors and actions to engage peers in prevention


Other Outcome Measures:
  • Violence acceptance [ Time Frame: Up to 60 months ]
    Attitudes toward gaining consent for sexual activity and Abbreviated Illinois Rape Myth Acceptance Scale

  • Cost Measures [ Time Frame: Up to 60 months ]
    Costs associated with training/program start-up and implementation, including the cost of training supplies, personnel (trainers and administrators), continuing education, and program monitoring. Given that colleges will be recruited from multiple geographic regions, cost of living adjustments will be included in the analysis. The economic analyses will use estimates of program effectiveness, together with economic measures of program costs, to estimate the incremental cost-effectiveness of the programs from college, student, and societal perspectives. Within-condition cost-effectiveness will be estimated for periods of 1-4 years based on observed differences in reported frequency of sexual violence events, health-related outcomes, and program costs across campus settings and over time.


Estimated Enrollment: 24
Study Start Date: January 2016
Estimated Study Completion Date: December 2019
Estimated Primary Completion Date: December 2019 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Green Dot BIC 1

Bystander Intervention Components Clusters will include at least a component of Green Dot.

E.g. Comparisons will be made across schools that have Green Dot versus those that don't have Green Dot. (BIC 1)

Behavioral: BIC 1
BIC cluster creation will include policy, implementation and degree of community coverage, specific title mandatory, and exclusively online training.
Online BIC 2

Bystander Intervention Components Clusters will include at least a component of online bystander training.

E.g. Comparisons will be made across schools that have online bystander training versus those that do not. (BIC 2)

Behavioral: BIC 2
BIC cluster creation will include policy, implementation and degree of community coverage, specific title mandatory, and exclusively online training.
Alternative programs BIC 3

Bystander Intervention Components Clusters will include at least a component of Green Dot.

E.g. Comparisons will be made across schools that have alternative program versus those that do not. (BIC 3)

Behavioral: BIC 3
BIC cluster creation will include policy, implementation and degree of community coverage, specific title mandatory, and exclusively online training.

  Show Detailed Description

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 24 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Public universities with junior faculty to be mentored in violence prevention Note: sampling unit for primary analyses is the college: answers to questions below refer to students clustered at each institution
Criteria

Inclusion Criteria at College level:

  • Public universities with junior faculty to be mentored in violence prevention

Exclusion Criteria:

  • Private universities, institutions with less than 10,000 undergraduate students

Inclusion Criteria at Student level:

  • Undergraduate students at the public 4 year colleges or universities, ages 18-24

Exclusion Criteria:

  • Graduate or professional students, non-degree seeking or not enrolled
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02659423


Locations
United States, Kentucky
University of Kentucky
Lexington, Kentucky, United States, 40536-0293
Sponsors and Collaborators
Ann Coker
Centers for Disease Control and Prevention
Investigators
Principal Investigator: Ann L Coker, PhD University of Kentucky
Principal Investigator: Heather M Bush, PhD University of Kentucky
  More Information

Responsible Party: Ann Coker, Verizon Wireless Endowed Chair Department of Obstetrics and Gynecology, in the University of Kentucky College of Medicine and Professor of Epidemiology in the Department of Epidemiology, in the UK College of Public Health, University of Kentucky
ClinicalTrials.gov Identifier: NCT02659423     History of Changes
Other Study ID Numbers: RFA-CE-15-003
First Submitted: January 11, 2016
First Posted: January 20, 2016
Last Update Posted: January 26, 2017
Last Verified: January 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Ann Coker, University of Kentucky:
Bystanding behaviors
Campus
Prevention
Sexual Assault
CampusSave