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Which works better: doctor or family telling relatives about genetic risk?

NCT ID NCT05348564

First seen Apr 30, 2026 · Last updated Jun 06, 2026 · Updated 7 times

Summary

This study looks at the best way to inform family members about their risk for two inherited conditions: Long QT Syndrome and Familial Hypercholesterolemia. Researchers will compare having the study team directly contact relatives versus asking the patient to contact them. About 200 adults who carry a specific gene variant will participate, and their first-degree relatives can get free, at-home genetic testing.

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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

  • University of Maryland Amish Research Clinic

    RECRUITING

    Lancaster, Pennsylvania, 17602, United States

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

Conditions

The condition(s) this trial relates to.

Hyperlipoproteinemia Type II long QT syndrome

As listed by the trial registrant

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