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NCT05162846Completed

Michigan Genetic Hereditary Testing (MiGHT)

Methods for Increasing Genetic Testing Uptake in Michigan

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

The primary purpose of this study is to compare three interventions, two experimental and one standard of care (usual care), to see if the experimental interventions will increase the likelihood of a participant obtaining guideline-concordant genetic testing. Eligible participants will be randomized (assigned) to one of the following interventions: 1) Virtual genetics navigator, a mobile-optimized website, designed by the investigators, that delivers tailored messages and content; 2) two motivational interviewing (MI) telephone calls delivered by trained genetics health coaches; or 3) usual care.

Status (registry)
Completed
Study type
Interventional
Enrollment
793 (actual)
First submitted
8 Dec 2021
Start date
21 Apr 2022
Primary completion date
13 Jul 2025
Lead sponsor
University of Michigan Rogel Cancer Center
NCT number
NCT05162846

What you commit to

  • Study type: Interventional
  • Participants enrolled: 793
  • From 21 Apr 2022 to the primary completion date, 13 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior clinical germline genetic testing for cancer or already have an upcoming appointment scheduled with a genetics provider

Who the study is looking for

  • Able to speak and read English
  • Access to the internet
  • Completed the Family Health History Tool (FHHT)
  • Meeting clinical criteria for genetic evaluation due to any of the below:
    • Personal history of Breast cancer either:
    • i. Diagnosed under 50
    • ii. Personal or family history of triple negative breast cancer
    • iii. Ashkenazi Jewish ancestry
    • iv. Male proband
    • v. 1st or 2nd degree relative with ovarian cancer, pancreatic cancer, breast cancer diagnosed under 50, or male breast cancer
    • Personal history of prostate cancer either:
    • i. Diagnosed under 50
    • ii. Ashkenazi Jewish ancestry
    • iii. 1st or 2nd degree relative with ovarian cancer, pancreatic cancer, breast cancer diagnosed under 50, or male breast cancer
    • Personal history of any cancer or no personal history of cancer with either:
    • i. PREMM score ≥ 2.5%
    • ii. 1st degree relative with pancreatic, or male breast cancer
    • iii. 1st or 2nd degree relative with ovarian cancer
    • iv. 1st degree relative with any of these cancers diagnosed under 50: colon, endometrial, or breast
    • v. Ashkenazi Jewish ancestry and 1st or 2nd degree relative with breast cancer
    • Personal history of endometrial cancer diagnosed under 50
    • Personal history of colorectal cancer diagnosed under 50
    • Personal history of renal cancer diagnosed under 46
    • Personal history of sarcoma diagnosed under 46 and a 1st or 2nd degree relative with sarcoma, breast cancer, or brain cancer diagnosed under 56
    • Personal history of brain cancer diagnosed under 46 and a 1st or 2nd degree relative with sarcoma, breast cancer, or brain cancer diagnosed under 56
    • Personal history of any two of the following cancers with at least one of them diagnosed under 46: breast, sarcoma, or brain
    • Personal history of ovarian cancer
    • Personal history of pancreatic cancer
    • Personal history of adrenal cortical carcinoma

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Michigan Rogel Cancer Center
Coordinator of this site? Confirm its status
Ann ArborUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.