No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
45 – 74
Sex
Female
Study type
Interventional
Purpose
Screening
Participants needed
820 (estimated)
Sponsor
Georgetown University · Other
Who this trial is looking for
This trial is looking for women aged 45-74 who identify as Black/African American or Hispanic/Latin(e)(a) and are interested in breast and colon cancer screening. Participants will receive help with navigating these screenings and may be asked to complete surveys during the study.
Are You a Good Fit for This Trial?
You may be able to join if
I am seeking screening navigation services at a participating site.
I am due for breast cancer screening and also eligible for colorectal cancer screening.
I am female.
I am aged 45 to 74.
I identify as Black/African American or Hispanic/Latin(e)(a).
I speak English or Spanish well enough to complete study activities.
I am willing to comply with all study procedures.
I can provide a completed electronic informed consent form.
You may not be able to join if
I am not planning to use the navigation programs at the participating sites.
I am not eligible for breast cancer screening or not due for colorectal cancer screening.
I have a history of breast and/or colorectal cancer or have related symptoms.
I am male, intersex, or identify as another sex.
I am under 45 or over 74 years old.
I do not identify as Black/African American or Hispanic/Latin(e)(a).
I do not speak English or Spanish well enough to complete study activities.
I am unwilling to comply with study procedures or cannot be available throughout the study.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 m…
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.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
1. Seeking screening navigation services through programs at a participating site (Georgetown Lombardi Cancer Center or Helen F. Graham Cancer Center \& Research Institutes)
2. Eligible for breast cancer screening while also due and eligible for colorectal cancer screening (per …
Inclusion Criteria:
1. Seeking screening navigation services through programs at a participating site (Georgetown Lombardi Cancer Center or Helen F. Graham Cancer Center \& Research Institutes)
2. Eligible for breast cancer screening while also due and eligible for colorectal cancer screening (per USPSTF guidelines)
3. Female sex
4. Aged 45-74
5. Identify as Black/African American race and/or Hispanic/Latin(e)(a) ethnicity
6. Speak English or Spanish with enough fluency to complete study activities
7. Stated willingness to comply with all study procedures (navigation, surveys) and availability for the duration of the study
8. Provision of completed electronic informed consent form
Exclusion Criteria:
1. Not engaged with or planning to use navigation programs at Georgetown Lombardi Cancer Center and Helen F. Graham Cancer Center \& Research Institute
2. Not eligible for breast cancer screening or not due and eligible for colorectal cancer screening (per USPSTF guidelines)
3. History of breast and/or colorectal cancer; or Reporting symptoms related to breast and/or colorectal cancer (e.g., GI bleeding, breast mass)
4. Male sex, Intersex, or other sex
5. Under age 45 or over age 74
6. Identifies as neither Black/African American race nor Hispanic/Latin(e)(a) ethnicity
7. Speaks neither English nor Spanish with enough fluency to complete study activities
8. Stated unwillingness to comply with study procedures (navigation, surveys) or unavailability for the duration of the study
9. Inability to provide electronic informed consent, or needing another person to authorize informed consent on their behalf
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