此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Cascade Testing In Identifying At-risk Family Members Of Individuals With Familial Hypercholesterolemia (FH) In PCP

2026年9月16日 更新者:Isa J. Houwink、Mayo Clinic

A Cluster Randomized Controlled Trial To Evaluate The Efficacy Of Cascade Testing In Identifying At-risk Family Members Of Individuals With Familial Hypercholesterolemia (FH) In PCP

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).

研究概览

详细说明

  1. Index Patient Genetic Testing (only index patients from the REP database):

    • Index patients identified through the REP database will undergo confirmatory FH testing HCHLG panel
    • A sputum collection kit is mailed to participants along with a pre-addressed return mailer.
    • Results are recorded in the electronic medical record and communicated to index (REP) participants with next-step instructions.
    • Only index patients with confirmed pathogenic/likely pathogenic variants proceed in the study.
  2. Relative Genetic Testing:

    • Relatives in the intervention arm who contact the study team and consent will be mailed a Focused Molecular Targeted Test (FMTT) sputum kit.
    • Testing targets the specific FH variant identified in the corresponding index patient.
    • Testing costs are covered **only** for relatives in the intervention arm.
    • Control arm relatives may choose to pursue clinical genetic testing independently through their primary care provider referring them to genetic counselling (usual care).
  3. Baseline Data Collection (Index Patients):

    • Collection of demographics and FH-related history via REDCap.
    • LDL-C values abstracted from EMR; ROI used if external records are required.
  4. Randomization:

    • Index patients randomized 2:1 to intervention or control arm.
    • Randomization occurs only after completion of baseline survey.
  5. Intervention Arm Procedures:

    Indirect contact:

    In the CASCADE-FH trial, index patients receive IRB-approved recruitment letters, with contact information for the primary care study team, to distribute to up to three first- or second-degree relatives. Relatives who contact the team undergo screening and electronic consent. In this study, index patients choosing the indirect pathway are provided with structured Mayo approved educational materials to support the index patient in accurate and consistent communication with relatives.

    Direct Contact:

    In the CASCADE-FH trial, modified direct contact is operationalized through an IRB approved recruitment letter sent by the index patient to their relatives with contact information for the primary care study team. No direct outreach from the study team occurs unless a relative independently initiates contact to the study team.

    Relatives who contact the team undergo screening and electronic consent. After consent the primary care study team will be able to provide direct support to the at-risk relatives, provide Mayo-approved patient educational materials, and inform them of their potential risk for FH and the opportunity for genetic testing. This approach allows the primary care study team to provide a more direct method of communication and interaction with the at-risk relatives. The study team will also facilitate genetic testing, should the relative wish to proceed with genetic testing for FH.

    • Intervention-arm relatives receive FMTT sputum kits paid for by the study.

  6. Control Arm Procedures:

    • Index patients receive usual care. No structured outreach is provided.
    • Relatives may seek genetic testing for FH through their primary care provider referring them to genetic counselling.
    • The study does not cover genetic counseling or testing costs in the control arm.
  7. Relative Procedures (All Arms):

    • Relatives who contact the research team receive full study information and undergo screening and consent.
    • Baseline surveys collected via REDCap.
    • Minors require parental consent and age-appropriate assent.
  8. Follow-Up Surveys:

    • Index patients and relatives receive surveys at 1, 3, and 12 months via REDCap.
    • Up to two reminder emails are sent approximately 7 days apart.
    • Participants who do not respond after reminders are classified as lost to follow-up.
  9. Genetic Testing Workflow:

    • Returned sputum kits will be processed.
    • Results entered into EMR for all participants.
    • index (REP) participants and relatives in the intervention arm are notified via secure message or email on next steps.

      • Index (REP) participants who test positive are instructed to follow up with their primary care provider.
      • Follow-up for Positive Findings for Relatives in the intervention arm:

Participants who receive a pathogenic or likely pathogenic result for FH will be notified via secure patient portal or email. Notifications will instruct the participant to contact their primary care provider for referral to genetic counseling and/or preventive cardiology.

Parents or guardians of minors aged 1-18 years who test positive will be instructed to contact the child's primary care provider to obtain referral to a pediatric endocrinologist.

研究类型

介入性

注册 (估计的)

480

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Family Medicine Research Study Coordinators
  • 电话号码:507-422-6823
  • 邮箱:RSTFMSC@mayo.edu

学习地点

    • Minnesota
      • Rochester、Minnesota、美国、55905
        • Mayo Clinic in Rochester
        • 接触:
          • Family Medicine Research Study Coordinators
          • 电话号码:507-422-6823
          • 邮箱:RSTFMSC@mayo.edu
        • 首席研究员:
          • Elisa J. Houwink, MD, PhD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

不

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Usual Care
Patients will receive standard of care support
No structured outreach is provided to patient or family members. Relatives may have their primary care provider refer them to genetic counseling services for cascade testing coordination.
实验性的:Structured Outreach
Patients and relatives will receive outreach in the form of direct or indirect contact

Patient relatives will be contacted either directly or indirectly per patient preference:

The indirect contact method provides patients with structured Mayo approved educational materials to support the index patient in accurate and consistent communication with relatives. Relatives have the option to contact the study team for cascade genetic testing.

The direct contact method provides patients with a letter inviting relatives to contact the study team. After contact, relatives are offered educational materials and the opportunity for cascade genetic testing.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Genetic testing among first- and second-degree relatives within 12 months of index patient enrollment
大体时间:2 year
Defined as total number of relations to complete CLIA-certified FH test (LDLR, APOB, PCSK9, LDLRAP1) with result returned to the primary care research team.
2 year

次要结果测量

结果测量
措施说明
大体时间
Number of newly diagnosed FH cases among relatives
大体时间:2 years
Total number of patient relatives newly diagnosed with familial hypercholesterolemia (FH)
2 years
Time from index patient enrollment (Tapestry identified participants) and diagnosis (REP identified and FH genetic test confirmation) to relative testing
大体时间:2 years
Number of days between patient enrollment and testing of relatives
2 years
Time from relative diagnosis to treatment initiation
大体时间:2 years
Number of days between diagnosis and start of treatment
2 years
Communication modality preference
大体时间:2 years
letter sent by the index patient to their relatives with contact information for the primary care study team. the indirect pathway are provided with structured Mayo approved educational materials to support the index patient in accurate and consistent communication with relatives.
2 years
Referral completion (genetics, cardiology, preventive cardiology) within 6 months of positive result
大体时间:2 years
Number of patients to be referred to specialty within 6 months of positive result
2 years
Cascade depth (degree of relatives reached)
大体时间:2 years
Degree of relatives reached (1st, 2nd, 3rd)
2 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

调查人员

  • 首席研究员:Elisa J. Houwink, MD, PhD、Mayo Clinic

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月20日

初级完成 (估计的)

2028年6月20日

研究完成 (估计的)

2029年9月20日

研究注册日期

首次提交

2026年6月2日

首先提交符合 QC 标准的

2026年6月12日

首次发布 (实际的)

2026年6月17日

研究记录更新

最后更新发布 (实际的)

2026年9月18日

上次提交的符合 QC 标准的更新

2026年9月16日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅