Closing the GAPS: Guideline Adherence, Prevention and Surveillance in Hereditary Cancer

Running, not enrolling · Not applicable

Conditions studied: Hereditary Cancer Syndromes, Clinical Decision Support

In brief

The goal of this clinical trial is to see if a software platform can improve cancer screening in young adults with genetic risk for cancer. The trial will also help improve the software platform (Nest). The main questions it aims to answer are: * Do Nest users know more about their cancer risks and recommended care than non-users? * Do Nest users have less psychological distress than non-users? * Do Nest users share cancer risks with family and other doctors more than non-users? * Are Nest users more likely than non-users to have up-to-date care plans? Researchers will compare Nest users to non-users to see if the Nest users are more likely to do recommended cancer screening. Participants will: * Have a genetic counseling or follow up visit * Take a post-visit survey * Intervention arm only: use the Nest Patient Navigator * Complete screening and follow-up care recommended by doctors

Key facts

Study ID
NCT06654466
Run by
Nest Genomics
People needed
100
Starts
2026-02-10
Expected to finish
2027-09-01
Last updated by the study team
2026-07-16

Who can join

Age: 18 and older, up to 49. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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