Actively Recruiting

Phase Not Applicable
Age: 13Years +
All Genders
Healthy Volunteers
ID05768217

Community Resiliency Collective Efficacy Intervention (CRCEI) for Prevention of Community Violence - A Cluster Randomized Controlled Trial

Led by University of Pittsburgh · Updated on 2026-06-04

4600

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

C

Centers for Disease Control and Prevention

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness of a community-centered intervention called the Community Resiliency Collective Efficacy Intervention (CRCEI) to promote thriving and resiliency and reduce community violence. This study uses a cluster-randomized controlled trial design involving diverse neighborhoods in the Pittsburgh region, engaging youth aged 13 to 19 years and adult community members of all genders. The intervention focuses on neighborhood transformation, racial and gender equity, community leadership, and social change to increase collective efficacy and reduce violence. The CRCEI intervention includes 9 sessions, starting with 2 discussion sessions about community thriving followed by a 7-week training program covering topics such as community strengths, collective efficacy, violence prevention, peaceful intervention strategies, police-community roles, communication skills, and community resources. Comparison neighborhoods will receive 9 health education sessions covering various community-identified health topics as a control intervention. Participants will complete surveys to measure changes in perceptions of neighborhood collective efficacy and community cohesion approximately 12 months after baseline. Other assessments include tracking community violence incidence over 1 to 2 years and self-reported violence exposure. Qualitative interviews and observations will gather information on program implementation. The study duration extends to about 2 years, with safety and community impact monitored throughout.

CONDITIONS

Brief Title

Community Resiliency Collective Efficacy Intervention

Who Can Participate

Age: 13Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth age 13 years old and up (all genders)
  • Adults 18 years and older (all genders)
  • Reside in neighborhoods selected to participate in the study
Not Eligible

You will not qualify if you...

  • Individuals younger than 13 years old
  • Individuals residing outside of participating neighborhoods

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 9 weeks

Participants engage in either the Community Resiliency Collective Efficacy Intervention, which includes 2 discussion sessions and a 7-week training program on community thriving and social change, or health education sessions as a control intervention.

9 sessions over approximately 9 weeks

Long-term Monitoring

Duration - Approximately 12 months

Participants are observed for changes in neighborhood collective efficacy, community cohesion, and incidence of community violence over approximately 12 months after the intervention.

Periodic survey assessments during follow-up

Trial Site Locations

Total: 1 location

1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

C

Christi Gomez

E

Elizabeth Miller, MD, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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