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 Apr 25, 2026 · Updated 24 times
Summary
This study tests whether a Parent Navigator Program 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 the navigator program or standard care. Researchers will track clinic visits, child development, and parent stress over 6 months.
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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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Study contacts
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Contact
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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