跳至主要内容
临床试验/NCT05768217
NCT05768217招募中不适用

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

University of Pittsburgh2 个研究点 分布在 1 个国家目标入组 4,600 人开始时间: 2024年6月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
4,600
试验地点
2
主要终点
Change from baseline in perceptions of neighborhood collective efficacy and community cohesion

研究概览

简要总结

This study will evaluate, via a cluster-randomized controlled trial, the effectiveness of a community-centered intervention that promotes thriving and resiliency to reduce community violence.

详细描述

This study will evaluate, via a cluster-randomized controlled trial, the effectiveness of an innovative community-centered intervention that promotes thriving and resiliency to reduce community violence. In collaboration with community partners, this study will implement a Community Resiliency Collective Efficacy Intervention (CRCEI) to engage community members in dialogue on neighborhood transformation, racial and gender equity, community leadership, and organizing for social change. Facilitating discussion and community organizing within neighborhoods about child and youth thriving is expected to increase individual and neighborhood levels of collective efficacy and reduce community violence. Using a community-partnered participatory approach, this study will use a Community Thriving Matrix tool to engage youth and adult community members in ongoing dialogue on neighborhood transformation, community leadership, and organizing for social change. This focus on envisioning and creating neighborhoods in which children and adolescents can thrive is expected to translate to increased individual and neighborhood levels of collective efficacy as well as violence reduction. Comparison neighborhoods will receive health education sessions as a control intervention. The proposed study involves diverse neighborhoods in the Pittsburgh region and collecting survey data from youth (ages 13-19 years) and adult community participants (both male and female identified). Interviews with a sub-sample of community residents and facilitators and community site leads as well as observations of intervention delivery will provide qualitative information on processes of program implementation. This study will provide the first rigorous evaluation of this community-level prevention approach.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
13 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

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

研究组 & 干预措施

Community Resiliency Collective Efficacy Intervention (CRCEI)

Experimental

Community Resiliency Collective Efficacy Intervention (CRCEI) to engage community members in dialogue on thriving, community leadership, and organizing for social change (9 sessions).

干预措施: Community Resiliency Collective Efficacy Intervention (CRCEI) (Behavioral)

Health Education Sessions

Active Comparator

Comparison neighborhoods will receive health education sessions as a control intervention. (9 sessions)

干预措施: Health Education Sessions (Behavioral)

结局指标

主要结局

Change from baseline in perceptions of neighborhood collective efficacy and community cohesion

时间窗: Change from baseline to approximately 12 months after baseline

Composite Measure mean score (range 1 - 5; 1 is low and 5 is best) of neighborhood-level perceptions of collective efficacy and community cohesion

次要结局

  • Change from baseline in collective efficacy and neighborhood social norms(Change from baseline to approximately 12 months after baseline)
  • Community incidence of violence in 12 month period(Change from 1 year period before baseline to approximately 2 years after baseline)
  • Number of self-reported events of violence exposure(Change from baseline to approximately 12 months after baseline)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Alison Culyba

Associate Professor

University of Pittsburgh

研究点 (2)

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