New program aims to keep High-Risk patients on track for cancer prevention

NCT ID NCT07565467

First seen May 13, 2026 · Last updated Jun 23, 2026 · Updated 6 times

Summary

This study tests a program to help people with inherited genetic mutations that raise their cancer risk stick to recommended screening schedules. Researchers will interview 80 women with BRCA or Lynch syndrome mutations and track how well they follow cancer surveillance guidelines. The goal is to lower their risk of developing cancer through better adherence to care.

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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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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • MD Anderson Cancer Center

    Houston, Texas, 77030, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this could lead to better ways to help people with genetic cancer risks stick to screening and reduce their chances of getting cancer.

What could go wrong

This is an early, small study (80 people) that focuses on interviews and standard care, not a new treatment. It may not show clear benefits or apply to everyone.

Conditions

The condition(s) this trial relates to.

hereditary neoplastic syndrome

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.