NCT03392597

Brief Summary

This research will examine if participation in a strengths-based curriculum, the Brothers as Allies program adapted from the Council for Boys and Young Men, reduces risk for future sexual violence perpetration among middle school-aged boys in New York State.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
720

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2017

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 26, 2017

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

August 3, 2017

Completed
5 months until next milestone

First Posted

Study publicly available on registry

January 8, 2018

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 24, 2020

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 29, 2020

Completed
Last Updated

March 15, 2019

Status Verified

March 1, 2019

Enrollment Period

3 years

First QC Date

August 3, 2017

Last Update Submit

March 14, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • Sexual violence perpetration (Koss et al., 2006)

    This will be measured by items from a widely used measure of sexual violence perpetration behaviors

    3 months

Study Arms (2)

Brothers as Allie

EXPERIMENTAL

Brothers as Allies is a strengths-based group approach to promote boys' and young men's safe and healthy passage through the pre-teen and adolescent years by addressing rigid beliefs and norms about masculinity that are harmful to the health, safety, relationships and opportunities of boys and young men. Groups of six to ten boys of similar age and development meet weekly with one or two facilitators for 1.5 to 2 hours for ten or more weeks. Meetings include warm up activities, an opportunity for check-in, experiential activities that address gender relevant topics (e.g., group challenges, games, skits, role plays), and a reflection and group dialogue component.

Behavioral: Brothers as Allies

Programming-as-Usual

ACTIVE COMPARATOR

Usual programming implemented in afterschool programs.

Behavioral: Programming-as-Usual

Interventions

Strengths-based group approach to promote boys' and young men's safe and healthy passage through the pre-teen and adolescent years.

Brothers as Allie

Usual afterschool programming.

Programming-as-Usual

Eligibility Criteria

Age12 Years - 14 Years
Sexmale(Gender-based eligibility)
Gender Eligibility DetailsMiddle school-aged boys
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Participants must be males of middle school age (12-14 years), participating in afterschool/youth programming at one of the intervention or control sites.

You may not qualify if:

  • None.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Planned Parenthood of Central and Western New York

Rochester, New York, 14605, United States

RECRUITING

Study Officials

  • Janis Whitlock, PhD

    Cornell University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
CROSSOVER
Model Details: Waitlist control design in which matched sites are randomly assigned to an intervention or waitlist control group to implement and evaluate the Brothers as Allies program. Intervention groups will participate in the Brothers as Allies program from the Council for Boys and Young Men. Waitlist control groups will participate in programming-as-usual until implementation with the intervention groups is complete, at which point they will receive the intervention. All participants will complete surveys at baseline, immediate post-intervention, and at 3 and 6 months post-intervention.
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Scientist

Study Record Dates

First Submitted

August 3, 2017

First Posted

January 8, 2018

Study Start

July 26, 2017

Primary Completion

July 24, 2020

Study Completion

September 29, 2020

Last Updated

March 15, 2019

Record last verified: 2019-03

Locations