Clin2
NCT07318363Possibly a fitNot yet recruiting

Improving genetic testing in families with hereditary cancer

CommunicationInformed Decision-making

This study looks at whether helping people with hereditary cancer genetic changes (like BRCA or Lynch syndrome) communicate with their at-risk relatives leads to more family members getting tested. It aims to improve cancer prevention and early detection.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
2,100 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years old or older.
  • You live in the United States.
  • You speak and read English or Spanish.
  • You have internet or phone access with a US number for email or text.
  • You either carry a genetic change (in BRCA1, BRCA2, MLH1, MSH2, MSH6, or PMS2) OR are a close relative of someone who does.
  • You can provide contact information for at least one at-risk relative to invite into the study (for patients).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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