Connecting Black families in Houston to genetic counseling and testing for cancer risk
Connecting Black Families in Houston, Texas to Hereditary Cancer Genetic Counseling, Genetic Testing, and Cascade Testing by Using a Simple Genetic Risk Screening Tool and Telegenetics
This study is trying to connect Black families in Houston to genetic counseling and testing for breast and colorectal cancer risks to see if it helps them understand their health better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT05694559 on ClinicalTrials.gov |
What this trial studies
This study aims to identify Black individuals eligible for genetic testing for hereditary cancer risks, specifically breast and colorectal cancer, through a validated genetic risk screening tool. By collaborating with trusted community organizations, the study seeks to enroll 300 Black families, providing genetic counseling and testing to those identified as at risk. Participants will receive information about their genetic risk, options for testing, and resources for family cascade testing if necessary. The approach includes both on-site and remote genetic testing to enhance accessibility.
Who should consider this trial
Good fit: Ideal candidates for this study are Black or African-American individuals over 18 years old who are interested in understanding their hereditary cancer risks.
Not a fit: Patients who do not self-identify as Black or African-American will not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could significantly improve cancer risk awareness and prevention among Black families.
How similar studies have performed: Other studies have shown success in using community-based approaches for genetic testing and counseling, making this approach both relevant and promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Any participant over 18 years old who self-identifies as Black or African-American and signs an informed consent form, also referred to as the 'Permission to Contact' form, to be part of our study. Exclusion Criteria: None
Where this trial is running
Houston, Texas
- MD Anderson Cancer Center — Houston, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Banu Arun, MD — MD Anderson Cancer Cneter
- Study coordinator: Banu Arun, MD
- Email: barun@mdanderson.org
- Phone: 713-792-2817
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.