New program aims to boost family communication about genetic risks
NCT ID NCT07318363
First seen Jan 08, 2026 · Last updated May 05, 2026 · Updated 17 times
Summary
This study tests a program that helps people with certain genetic mutations talk to their relatives about testing and treatment. It compares the program to standard care for 2100 adults in the US. The goal is to improve informed decision-making and family communication.
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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.
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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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The University of Texas M. D. Anderson Cancer Center
Houston, Texas, 77030, United States
Conditions
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