RightFit
RecruitingNot applicable

Bundled Cancer Screening and Genetic Services Navigation

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
45 Years to 74 Years
Sex
Female only
Healthy volunteers
Accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests help with getting breast and colon or rectal cancer screening together, compared with help for breast screening alone. For those who qualify, it also tests adding education before a referral for genetic services, which look at inherited cancer risk. It is for Black and/or Hispanic females ages 45–74 who qualify for breast screening and are also due for colon or rectal screening.

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.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Seek screening support through Georgetown Lombardi Cancer Center or Helen F. Graham Cancer Center & Research Institutes.
  • Qualify for breast cancer screening and be due and qualify for colon or rectal cancer screening under national guidelines.
  • Be female.
  • Be 45–74 years old.
  • Identify as Black/African American and/or Hispanic/Latin(e)(a).
  • Speak English or Spanish well enough to take part.
  • Agree to study activities, including screening support and surveys, and be available for the whole study.
  • Complete an electronic consent form agreeing to take part.

Who can't join

  • Do not use or plan to use screening support programs at either study site.
  • Do not qualify for breast screening, or are not due or do not qualify for colon or rectal screening.
  • Have had breast, colon, or rectal cancer, or have related symptoms, such as bleeding in the digestive tract or a breast lump.
  • Are male, intersex, or a sex other than female.
  • Are younger than 45 or older than 74.
  • Identify as neither Black/African American nor Hispanic/Latin(e)(a).
  • Do not speak English or Spanish well enough to take part.
  • Cannot agree to or complete study activities, are unavailable for the whole study, or cannot give electronic consent yourself.

Simplified for readability. The official criteria below are what the study team uses.

Official 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 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

Study sites (2)

DC

DE