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Bundled Cancer Screening and Genetic Services Navigation
Sponsor: Georgetown University
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.
Key Details
Gender
FEMALE
Age Range
45 Years - 74 Years
Study Type
INTERVENTIONAL
Enrollment
820
Start Date
2026-05-01
Completion Date
2029-05-31
Last Updated
2026-03-09
Healthy Volunteers
Yes
Interventions
Breast cancer screening navigation
Single cancer navigation includes the following, oriented to breast cancer only: cancer education, barrier assessment and resolution, screening exam scheduling, text and mail reminders, documentation of appointment completion and results communicated to patient.
Multicancer screening navigation
Multi-cancer navigation includes the following, oriented to breast and colorectal cancers: cancer education, barrier assessment and resolution, screening exam scheduling, text and mail reminders, documentation of appointment completion and results communicated to patient.
Usual care genetics referral
Referral for genetics will be provided at the completion of the navigation call.
Pretest education + usual care genetics referral
Print education regarding the genetic counseling and testing process and specific tips to support at-home testing. Referral for genetics will be provided at the completion of the navigation call.
Locations (2)
ChristianaCare-Helen F. Graham Cancer Center & Research Institute
Newark, Delaware, United States
Georgetown University
Washington D.C., District of Columbia, United States