Gene hunt: 689 volunteers help unlock cancer clues
NCT ID NCT02665195
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how certain gene changes may increase cancer risk. Researchers collect DNA and medical information from people with these gene changes and their family members. The goal is to give doctors better information to help families understand their cancer risks.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
689 people
The number who actually took part.
- Start date
-
Jan 2016
- Expected to finish
-
Jan 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This study will be conducted as a multi-center study with the involvement of attendings, genetic counselors, and research study staff at the participating institutions.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Individual with deleterious (pathogenic) or likely deleterious (likely pathogenic) mutation in a cancer susceptibility gene OR * Individual with a variant of uncertain significance (VUS) in a cancer susceptibility gene OR * Family members, either tested or not tested, who are part of a family known to be transmitting a deleterious or likely deleterious mutation or a variant of uncertain significance in a cancer predisposition gene Exclusion Criteria: * Inability or refusal to participate in consent discussion * Subject is less than 18 years old
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Genetic testing are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Dana Farber Cancer Institute
Boston, Massachusetts, 02115, United States
-
Mayo Clinic Cancer Center
Rochester, Minnesota, 55905, United States
-
Memorial Sloan Kettering @ Rockville
Rockville Centre, New York, 11570, United States
-
Memorial Sloan Kettering Basking Ridge
Basking Ridge, New Jersey, United States
-
Memorial Sloan Kettering Bergen
Montvale, New Jersey, 07645, United States
-
Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
-
Memorial Sloan Kettering Cancer Center @ Commack
Commack, New York, 11725, United States
-
Memorial Sloan Kettering Monmouth
Middletown, New Jersey, 07748, United States
-
Memorial Sloan Kettering Westchester
Harrison, New York, 10604, United States
-
University of Pennsylvania
Philadelphia, Pennsylvania, 19104-4283, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A phone call could unlock early cancer detection for High-Risk groups
- Emotional support may ease distress during cancer genetic testing
- Can a digital guide boost genetic testing in prostate cancer survivors?
- New genetic counseling method may help breast cancer patients decide on surgery
- Could a simple blood test predict lung danger in heart defect patients?
- Phone cards boost screening confidence for pregnant patients