Bundled Cancer Screening and Genetic Services Navigation (NCT07228000) | Clinical Trial Compass
RecruitingNot Applicable
Bundled Cancer Screening and Genetic Services Navigation
United States820 participantsStarted 2026-05-06
Plain-language summary
The goal of this study is to test bundled familial cancer risk assessment + multicancer (colorectal + breast) vs. single (breast) cancer navigation, using a wait list control for colorectal cancer screening referral and navigation. Among those eligible, this study will test usual care referral to genetic services vs. pretest education + usual care referral. The study also will assess how bundled multicancer navigation works and for whom it is most effective through a multisite, mixed-methods patient- and organization-level process evaluation.
Who can participate
Age range45 Years – 74 Years
SexFEMALE
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Inclusion criteria
✓. Seeking screening navigation services through programs at a participating site (Georgetown Lombardi Cancer Center or Helen F. Graham Cancer Center \& Research Institutes)
✓. Eligible for breast cancer screening while also due and eligible for colorectal cancer screening (per USPSTF guidelines)
✓. Female sex
✓. Aged 45-74
✓. Identify as Black/African American race and/or Hispanic/Latin(e)(a) ethnicity
✓. Speak English or Spanish with enough fluency to complete study activities
✓. Stated willingness to comply with all study procedures (navigation, surveys) and availability for the duration of the study
✓. Provision of completed electronic informed consent form
Exclusion criteria
✕. Not engaged with or planning to use navigation programs at Georgetown Lombardi Cancer Center and Helen F. Graham Cancer Center \& Research Institute
What they're measuring
1
Receipt of colorectal cancer screening
Timeframe: 6 months after navigation completion
2
Receipt of breast cancer screening
Timeframe: Six months after completion of navigation