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Achieving My Potential: A Randomized, Controlled Trial of a Telephone-Based Developmental Care Coordination System

NCT04118452 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 565

Last updated 2025-05-23

Study results available
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Summary

The proposed project is a randomized controlled trial of a telephone-based early childhood developmental care coordination system, in partnership with 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 for developmental evaluation, increasing the numbers of children deemed eligible for services, and increasing the number of children actually receiving interventions.

Conditions

  • Child Development
  • Health Services Research

Interventions

BEHAVIORAL

Telephone-based early childhood developmental care coordination

The 211LA care coordinator will review developmental screening results and provide referral recommendations to the family and use 211LA's extensive resource directory and agency relationships to identify appropriate referrals. The 211LA care coordinator will provide a report to the clinical provider containing recommendations for follow-up and a care coordination plan. The report will be scanned into the EMR (Electronic Medical Record) by clinic staff and be available for provider review. The 211LA care coordinator will also make all recommended referrals and will call the family monthly until 1) children begin receiving services, 2) families refuse services, or 3) children are deemed ineligible by service providers.

Sponsors & Collaborators

  • Kaiser Permanente School of Medicine

    collaborator OTHER

  • Virginia Commonwealth University

    collaborator OTHER

  • Information and Referral Federation of Los Angeles County (211 LA County)

    collaborator UNKNOWN

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

    collaborator NIH

  • University of California, Los Angeles

    lead OTHER

Principal Investigators

  • Paul J Chung, MD MS · Kaiser Permanente School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
11 Months
Max Age
42 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-17
Primary Completion
2023-05-23
Completion
2023-05-23

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04118452 on ClinicalTrials.gov