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Could you help unlock cancer genetics? NCI launches screening survey

NCT ID NCT07005297

First seen Nov 01, 2025 · Last updated Jun 20, 2026 · Updated 41 times

Summary

This study screens up to 1,000 people with personal or family histories of certain cancers or genetic syndromes to see if they qualify for one of six ongoing NCI genetics research studies. Participants fill out a 15-20 minute online questionnaire about their health, family history, and genetic test results. If eligible, they may be invited to join a study that involves providing medical records, samples, or interviews. No treatments are offered.

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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

  • National Cancer Institute

    Rockville, Maryland, 20850, United States

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

Conditions

The condition(s) this trial relates to.

cardiofaciocutaneous syndrome chordoma Congenital Bone Marrow Failure Syndromes Costello syndrome Fanconi anemia Legius syndrome Li-Fraumeni syndrome melanoma Melanoma, Cutaneous Malignant neoplasm pulmonary blastoma

As listed by the trial registrant

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