Clinical trial No longer in our active list Interventional Ages 25 and up Women only

Promoting genetic counseling for African American women at high risk for breast cancer

Official title: Promoting Genetic Counseling Among African American Women With a Family History of Breast Cancer

Run by University of Illinois at Chicago · NCT04378751 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study is testing whether a special video or a regular brochure can encourage African American women at high risk for breast cancer to attend genetic counseling.

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Quick facts

Study typeInterventional
Ages25 Years and up
SexWomen only
Enrollment106 (estimated)
SponsorUniversity of Illinois at Chicago
Academic / other
Locations2 sites (Chicago, Illinois and 1 other locations)
Trial IDNCT04378751 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are African American women aged 25 or older who are classified as high risk for breast cancer and have not previously received genetic counseling.

Probably not a fit

Patients who do not identify as African American, are under 25 years old, or have previously received genetic counseling 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 research project aims to enhance the attendance of genetic counseling among African American women who are at high risk for breast cancer. Utilizing a randomized control trial design, participants will be assigned to either receive a culturally targeted decision aid video or a standard informational brochure about genetic counseling. The study will assess the effectiveness of these interventions in promoting genetic counseling attendance and will also explore the influence of these interventions on participants' social and familial networks. The study involves a cancer genetic risk assessment as part of the intake process to identify eligible participants.

Why it matters

Potential benefit: If successful, this study could significantly increase the uptake of genetic counseling among high-risk African American women, potentially leading to earlier detection and better management of breast cancer.

How similar studies have gone: Other studies have shown success in using culturally targeted interventions to improve health outcomes in minority populations, suggesting that this approach may be effective.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Are female
2. Identify as African American
3. Are age 25 or older
4. Speak and understand English
5. Completed a cancer genetic risk assessment (CGRA) as part of clinic intake
6. Are classified as high risk for developing breast cancer per CGRA
7. Have not previously received genetic counseling

Exclusion Criteria:

1. Are not female
2. Do not identify as African American
3. Are age 24 or younger
4. Do not speak and understand English
5. Did not complete a cancer genetic risk assessment (CGRA) as part of clinic intake
6. Are not classified as high risk for developing breast cancer per CGRA
7. Have previously received genetic counseling

Where it's running

  • University of Illinois at Chicago Hospital and Ambulatory Clinics
    Chicago, Illinois, United States
    Recruiting
  • UIC Cancer Center
    Chicago, Illinois, United States
    Not yet recruiting

Study contacts

  • Principal investigator: Kent Hoskins, MD — University of Illinois at Chicago
  • Study coordinator: Kent Hoskins, MD
  • Email: khoski@uic.ed
  • Phone: 312-355-0496

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.