Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Helping families share hereditary cancer risk information and access genetic testing

Official title: Testing Effectiveness of Navigation Interventions to Increase Uptake of Cascade Genetic Testing Among Relatives of Individuals Diagnosed With Hereditary Cancer Syndromes

Run by University of Michigan Rogel Cancer Center · NCT06927947 · Data updated 2026-11-12

This project tries web-based navigation and communication tools to help adults with a known hereditary cancer gene and their adult biological relatives share risk information and make it easier for relatives to get genetic testing.

More Hereditary Malignant Neoplasm trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment625 (estimated)
SponsorUniversity of Michigan Rogel Cancer Center
Academic / other
Locations1 site (Ann Arbor, Michigan)
StatusRecruiting
StartedSeptember 23, 2025
Main results expectedSeptember 30, 2026
Study endsSeptember 30, 2026
Registry record updatedJune 15, 2026
Trial IDNCT06927947 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults who carry a clinically confirmed autosomal dominant pathogenic germline variant identified through the University of Michigan Cancer Genetics Clinic and their adult biological relatives who have not had genetic testing and have internet access and English proficiency.

Probably not a fit

People who already completed clinical germline genetic testing, who are not biological relatives, who lack internet access, or who cannot read/speak English are unlikely to receive benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional effort uses a virtual Cascade Genetic Testing Platform to deliver web-based communication, educational materials, and navigation support to probands with a confirmed pathogenic germline variant and their adult biological relatives. Probands must have been evaluated at the University of Michigan Cancer Genetics Clinic; relatives must be adults, English-speaking, have internet access, and not have completed clinical germline testing. The platform aims to overcome logistic and communication barriers that limit cascade testing uptake, with outcomes measured over a shortened 6-month follow-up. Participants complete surveys and use informational/communication tools designed to increase relatives' participation in genetic testing and follow-up with genetics providers.

Why it matters

Potential benefit: If successful, this approach could increase the number of at-risk relatives who learn their genetic status and take preventive or management steps.

How similar studies have gone: Previous cascade-testing efforts show modest baseline uptake (about 20–30%), and some navigation or web-based interventions have produced incremental gains, but fully virtual cascade platforms are still relatively new.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* PROBANDS: Clinically confirmed autosomal dominant pathogenic germline variant (PGV) associated with a hereditary cancer syndrome
* PROBANDS: Previous evaluation by the University of Michigan (U-M) Cancer Genetics Clinic
* PROBANDS: ≥ 18 years old
* PROBANDS: Able to speak and read English
* PROBANDS: Access to the internet
* RELATIVES: Biological relative of proband
* RELATIVES: ≥ 18 years old
* RELATIVES: Able to speak and read English
* RELATIVES: Access to the internet
* RELATIVES: Have not completed germline genetic testing, per self-report at baseline

Exclusion Criteria:

* RELATIVES: Prior clinical germline genetic testing for cancer or already have an upcoming appointment scheduled with a genetics provider, per self-report at baseline

Where it's running

  • University of Michigan Comprehensive Cancer Center
    Ann Arbor, Michigan, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.