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Provider-Mediated Communication of Genetic Testing Results to At-Risk Relatives of Cancer Patients to Improve Genetic Counseling and Testing Rates, Family HOPE Study

Family HOPE Study (Hereditary Lynch Syndrome Opportunities for Participation &Amp; Engagement)

Who can join

Ages 18 and older · All sexes · Healthy volunteers welcome

Inclusion Criteria:

* PATIENTS: Enrolled in City of Hope (COH) institutional review board (IRB) 07047 or have been seen by COH Genetics for genetic testing
* PATIENTS: Have an pathogenic/ likely pathogenic germline variant
* PATIENTS: Fluent in English
* PATIENTS: Age \>= 18 years
* PATIENTS: Willing to provide contact information for eligible first-degree relatives
* PATIENTS: \>= 2 first-degree relatives that are eligible for genetic testing and reside in the United States of America
* FIRST-DEGREE RELATIVES: Proband is a COH patient and has consented to this study
* FIRST-DEGREE RELATIVES: First-degree relative of proband
* FIRST-DEGREE RELATIVES: Resides within the United States
* FIRST-DEGREE RELATIVES: Has not undergone genetic testing for the known familial variant
* FIRST-DEGREE RELATIVES: Are fluent in English
* FIRST-DEGREE RELATIVES: Age \>= 18 years

Exclusion Criteria:

* PATIENTS: Unable to provide informed consent
* PATIENTS: =\< 2 at-risk first-degree relatives who are eligible for genetic testing and/or reside within the United States
* PATIENTS: Unwilling to provide contact information for family members
* FIRST-DEGREE RELATIVES: Unable or unwilling to provide informed consent
* FIRST-DEGREE RELATIVES: Have undergone genetic testing for the known familial variant
* FIRST-DEGREE RELATIVES: Resides outside of the United States

About the study

This clinical trial tests whether provider-mediated communication of genetic testing results to at-risk relatives of cancer patients can help improve genetic counseling and testing rates. Approximately 15% of people with cancer have an inherited form of cancer due to changes in a gene that they have inherited from one of their parents. These changes increase a person's risk for developing cancer. Most people who have an inherited harmful change in a cancer risk gene don't know that they have it and are therefore not able to get the health care that they need. The primary reason for this problem has been a lack of genetic counseling and testing for cancer patients and patients with a strong family history of cancer. Another reason for this lack of awareness is that, when cancer runs in a family, the patient who carries the gene change usually has to communicate the genetic risk information to their family members. When this process doesn't work well, family members may not know that they need to get genetic testing and then may not get potentially life-saving care. Provider-mediated contact to discuss genetic test results may help improve rates of genetic testing among at-risk relatives of patients with a family cancer syndrome.

What is being tested

• Best Practice (other)
• Electronic Health Record Review (other)
• Personal Contact (behavioral)
• Survey Administration (other)

Sponsor: City of Hope Medical Center · Participants: 240 · Started: Feb 14, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT05772130

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.