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临床试验/NCT05567250
NCT05567250已完成不适用

Testing a Scalable Model For ACEs-Related Care Navigation Via 211 Telephone-Based Services

University of California, Los Angeles1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2022年10月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
102
试验地点
1
主要终点
Referrals to ACEs-related services

研究概览

简要总结

The study is a randomized controlled trial of a telephone-based care coordination system for families who experienced Adverse Childhood Events (ACEs). The investigators will conduct the study in partnership with Kaiser Permanente School of Medicine (KPSOM) and 2-1-1 Los Angeles County (211LA), part of a national network of 2-1-1 call centers covering 93% of the US population. The study will test the effectiveness of 211LA in increasing referrals and services for families who screen positive for ACEs.

详细描述

The trial will enroll 200 children ages 0-11 years from the three FQHCs partner clinics, who screen positive for at least 1 ACE during their clinical encounter. The research study team will randomize children 1:1 into intervention (connection to 211LA for ACEs care coordination + usual care) or control (usual care alone).

Primary outcomes will include number of referrals to, eligibility for, and receipt of ACE-related services among intervention group participants compared to controls.

The investigators will measure these outcomes through parent reported data and 211LA data at baseline and 6 months after enrollment.

Expected findings include higher referral and service rates by six months after enrollment among intervention group participants.

研究设计

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

入排标准

年龄范围
— 至 11 Years(Child)
性别
All
接受健康志愿者
是

入选标准

  • •A patient in one of the three partner community clinic systems (ChapCare, Via Care and NEVHC)
  • •Child aged 0 - 11 years old
  • •Parent or legal guardian of child at least 18 years of age
  • •Comfortable completing a survey by interview in English or Spanish

排除标准

  • •Child or sibling already enrolled in this study
  • •Child or sibling enrolled in the AMP Child Development study

研究组 & 干预措施

No Intervention: Usual Care

No Intervention

This group will receive usual care

Experimental Intervention + Usual Care

Experimental

Intervention group families will receive usual care and they will be connected via telephone to 211LA.

干预措施: Behavioral: Telephone-based ACEs care coordination (Behavioral)

结局指标

主要结局

Referrals to ACEs-related services

时间窗: 2-6 months after enrollment

The percentage of children who are referred to at least one ACEs-related service, as reported on the participant survey.

次要结局

  • Receipt of ACEs-related services(2-6 months after enrollment)
  • Number of referrals received(2-6 months after enrollment)
  • Number of services received(2-6 months after enrollment)

研究者

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

Rebecca Dudovitz, MD, MSHS

Associate Professor

University of California, Los Angeles

研究点 (1)

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