Improving genetic education and testing for Black cancer survivors
Official title: Addressing Genomic Disparities in Cancer Survivors
Run by Rutgers, The State University of New Jersey · NCT06073626 · Data updated 2026-11-12
This study is testing whether a chatbot can help Black cancer survivors learn more about genetic testing and encourage them to get tested compared to regular care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 350 (estimated) |
| Sponsor | Rutgers, The State University of New Jersey Academic / other |
| Locations | 2 sites (Washington D.C., District of Columbia and 1 other locations) |
| Status | Recruiting |
| Started | July 31, 2024 |
| Main results expected | June 30, 2027 |
| Study ends | August 31, 2027 |
| Registry record updated | November 9, 2026 |
| Trial ID | NCT06073626 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are Black or African American cancer survivors aged 18-80 who are at least six months post-diagnosis of specific cancers and meet genetic testing eligibility criteria.
✕Probably not a fit
Patients who do not speak English, have previously undergone genetic testing, or lack internet access may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to enhance genetic education and increase requests for genetic testing among Black cancer survivors through a chatbot intervention compared to enhanced usual care. Participants will be randomly assigned to either the chatbot group or the usual care group, with the study evaluating engagement levels and psychosocial outcomes. The research will involve 428 Black cancer survivors who meet specific genetic testing criteria, focusing on their experiences and decision-making processes regarding genetic testing. The study seeks to address disparities in genetic testing utilization within this population.
Why it matters
Potential benefit: If successful, this study could significantly improve access to genetic testing and education for Black cancer survivors, leading to better-informed health decisions.
How similar studies have gone: Other studies have shown success in using technology-based interventions to improve health education and outcomes, suggesting potential for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18-80 years of age * Self-identify as Black or African American * At least 6-months post diagnosis with any of the following cancers: breast, ovarian, uterine, prostate, colorectal, pancreatic * Have not had genetic testing for hereditary cancer * Have received care at one of the participating sites in the prior five years * Meet National Comprehensive Cancer Network criteria for germline GT * Able to read and speak in English * Capable of providing informed consent * Have internet access (via smartphone, tablet or computer) * Comfortable using a computer or mobile phone independently to access information Exclusion Criteria: * Do not speak English * Unable to access the Internet * Have previously undergone germline genetic testing for hereditary cancer risk or previously had genetic counseling (GC) and declined genetic testing (GT) * Are unable to provide informed consent
Where it's running
-
Georgetown Lombardi Comprehensive Cancer Center
Washington D.C., District of Columbia, United States Recruiting -
Rutgers Cancer Institute
New Brunswick, New Jersey, United States Recruiting
Study contacts
- Principal investigator: Anita Y Kinney, PhD, RN — Director at Rutgers Cancer Institute
- Study coordinator: Erin Speiser, PhD, MA
- Email: erin.speiser@rutgers.edu
- Phone: 732-675-1668
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.