Initial Testing of a Behavioral Intervention About Genetic Services for Families at Risk of Lynch Syndrome
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
The purpose of the study is to see if our education materials help people at risk for Lynch syndrome decide about seeking genetic services. Untested relatives of patients with Lynch syndrome will be recruited to complete a baseline survey and will be randomized to receive either the an information letter or an information letter plus a booklet. Two follow-up surveys will be administered over the span of 6 months. Participants will also be invited to join an optional exit interview to provide feedback.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Wiek co najmniej 18 lat
- •Mówisz po angielsku
- •Jesteś spokrewniony/a z osobą zdiagnozowaną ze zespołem Lyncha
- •Jesteś potencjalnie zagrożony/a zespołem Lyncha
- •Nie miałeś wcześniej porady genetycznej lub badania genetycznego w kierunku zespołu Lyncha
✗ Disqualifies
- •Przebytym nowotworem (z wyjątkiem czerniaka skóry)
- •Warunki utrudniające świadomy udział w badaniu, takie jak trudności poznawcze
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- July 21, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (1)
UAB
Birmingham, United States
Trial contact
Haoyang Yan, PhD
Kaylee Burgan, MS
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/22/2026.
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