Telephone-Based Care Coordination for Services Addressing Childhood Adversity

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorPaul Chung

About this trial

The goal of this study is to learn how telephone-based screening and care coordination impacts children experiencing adverse childhood events (ACEs). The main questions are:

1. Does telephone-based screening and care coordination for children experiencing ACEs increase child receipt of ACEs-related services? 2. Does telephone-based screening and care coordination for children experiencing ACEs improve parent health and wellbeing? 3. Does telephone-based screening and care coordination for children experiencing ACEs improve child social and emotional health?

Researchers will compare families who have been randomly selected to receive telephone-based screening and care coordination with those who will receive usual care at their clinic.

Participants will:

* Be randomly assigned to receive usual care or usual care plus telephone-based screening and care coordination (the intervention) * If selected for the intervention, be connected to 211 Los Angeles to receive screening and care coordination for up to 6 months * Complete four surveys via interview; surveys will be done at enrollment and 1 month, 6 months, and 12 months following enrollment * Agree to allow researchers to review their child's medical records to collect information about their child's health, screenings, diagnoses, and referrals.

Eligibility criteria

Qualifiers

Parent or legal guardian of focal child

Comfortable completing surveys in English or Spanish

Focal child is less than 12 years of age at enrollment

Disqualifiers

Focal child participated in the 'UCANN" pilot study

Focal child's sibling is enrolled in this study

Focal child is currently assigned a DCFS (Department of Child and Family Services) case worker

Trial design

Treatments tested in this trial

  • Telephone-based Screening and Care Coordination

Treatment groups

778 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Paul Chung

Lead sponsor

Kaiser Permanente

Sponsor institution

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator

University of California, Los Angeles

Collaborator

211 Los Angeles

Collaborator

Northeast Valley Health Corporation

Collaborator