Parent Navigator Program (PNP) to Improve Outcomes in Latino/x Children and Parents
Recruiting now · Not applicable
Conditions studied: Congenital Heart Disease
In brief
The goal of this clinical trial is to see if a Parent Navigator Program (PNP) is helpful for Latino/x parents of babies with congenital heart disease (CHD) to get connected to developmental follow-up services. The main question it aims to answer are: * Do families assigned to the Parent Navigator Program (PNP) have higher rates of connection to High-Risk Infant Follow-Up (HRIF)/Early Intervention (EI) compared to the standard care group 6 months after randomization? * Do children assigned to the Parent Navigator Program (PNP) have better neurodevelopmental outcomes (NDOs) compared to the standard care group 6 months after randomization? * Do parents assigned to the Parent Navigator Program (PNP) have decreased parental stress compared to the standard care group? Researchers will compare the Parent Navigator group to the standard care group to see if parent navigator group is helpful in connecting families to High-Risk Infant Follow-Up (HRIF)/Early Intervention (EI), improving neurodevelopmental outcomes (NDOs), and lowering parental stress. Participants will: * Undergo developmental assessments and survey at newborn stage and at 6 months * Participants randomly assigned to the Parent Navigator group will have weekly (at least) phone calls with the parent navigator * Participants randomly assigned to the Parent Navigator group will complete a 30-minute phone interview about their experience with the parent navigator program 6 months after random assignment
Key facts
- Study ID
- NCT07023367
- Run by
- Children's Hospital Los Angeles
- People needed
- 40
- Starts
- 2025-10-01
- Expected to finish
- 2026-06-30
- Last updated by the study team
- 2025-09-12
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Infants born with CHD requiring medical/surgical intervention at less than 30 days of age
- Identify as Latino/x
You may not qualify if…
- Presence of a major genetic syndrome
- Intraventricular hemorrhage or other major structural brain lesion
- Undergoing end of life care
- Parents of Latino/x Infants:
- Inclusion Criteria:
- Identify as Latino/x
- Exclusion Criteria:
- Not fluent in English or Spanish
Where it is running
- Children's Hospital Los Angeles — Los Angeles, California, United States (enrolling)
Full record on ClinicalTrials.gov
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