Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

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

16 septembre 2026 mis à jour par: 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).

Aperçu de l'étude

Statut

Pas encore de recrutement

Description détaillée

  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.

Type d'étude

Interventionnel

Inscription (Estimé)

480

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Family Medicine Research Study Coordinators
  • Numéro de téléphone: 507-422-6823
  • E-mail: RSTFMSC@mayo.edu

Lieux d'étude

    • Minnesota
      • Rochester, Minnesota, États-Unis, 55905
        • Mayo Clinic in Rochester
        • Contact:
          • Family Medicine Research Study Coordinators
          • Numéro de téléphone: 507-422-6823
          • E-mail: RSTFMSC@mayo.edu
        • Chercheur principal:
          • Elisa J. Houwink, MD, PhD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: 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.
Expérimental: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Genetic testing among first- and second-degree relatives within 12 months of index patient enrollment
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Number of newly diagnosed FH cases among relatives
Délai: 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
Délai: 2 years
Number of days between patient enrollment and testing of relatives
2 years
Time from relative diagnosis to treatment initiation
Délai: 2 years
Number of days between diagnosis and start of treatment
2 years
Communication modality preference
Délai: 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
Délai: 2 years
Number of patients to be referred to specialty within 6 months of positive result
2 years
Cascade depth (degree of relatives reached)
Délai: 2 years
Degree of relatives reached (1st, 2nd, 3rd)
2 years

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Elisa J. Houwink, MD, PhD, Mayo Clinic

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

20 octobre 2026

Achèvement primaire (Estimé)

20 juin 2028

Achèvement de l'étude (Estimé)

20 septembre 2029

Dates d'inscription aux études

Première soumission

2 juin 2026

Première soumission répondant aux critères de contrôle qualité

12 juin 2026

Première publication (Réel)

17 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

18 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

16 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner