Cascade Testing In Identifying At-risk Family Members Of Individuals With Familial Hypercholester… (NCT07653555) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Cascade Testing In Identifying At-risk Family Members Of Individuals With Familial Hypercholesterolemia (FH) In PCP
United States480 participantsStarted 2026-06-20
Plain-language summary
The purpose of this study is to evaluate the effectiveness of two models of cascade testing in identifying at-risk family members of individuals diagnosed with familial hypercholesterolemia (FH).
Who can participate
Age range
1 Year
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Index Patients:
* Age ≥ 18 years.
* Confirmed FH diagnosis using Dutch Lipid Clinic Network criteria \*or\* genetic confirmation.
* Identified through REP or Tapestry databases.
* Able and willing to provide informed consent.
* At least one eligible first- or second-degree relative.
* Access to and active use of email (computer literacy requirement).
Relatives:
* First- or second-degree relative of an enrolled index patient.
* Age ≥ 1 year (minors require parental consent + assent).
* Willing to participate and able to complete electronic consent (guardian-assisted if minor).
* Access to and active use of email (guardian).
Exclusion Criteria:
Index Patients:
* No confirmed FH diagnosis.
* Insufficient clinical follow-up (\<5 years).
* No identifiable or contactable relatives.
* Prior participation in structured cascade testing.
* Severe cognitive impairment preventing informed consent.
Relatives:
* Prior participation in structured cascade testing.
* Severe cognitive impairment preventing informed consent.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Genetic testing among first- and second-degree relatives within 12 months of index patient enrollment