Parent navigator program aims to boost developmental care for latino/x infants with heart disease
NCT ID NCT07023367
First seen Nov 01, 2025 · Last updated Jun 05, 2026 · Updated 30 times
Summary
This study looks at whether a Parent Navigator Program (PNP) helps Latino/x parents of babies with congenital heart disease connect to developmental follow-up services. About 40 families will be randomly assigned to either receive regular support from a parent navigator or standard care. Researchers will track how many visits families make to high-risk infant follow-up and early intervention clinics, measure the babies' development at 6 months, and check parents' stress levels.
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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Children's Hospital Los Angeles
RECRUITINGLos Angeles, California, 90027, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
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