Empowering Vulnerable and Resilient Latinas to Obtain Breast Cancer Care

Recruiting now · Not applicable

Conditions studied: Breast Cancer

In brief

The investigator and study staff will identify, recruit and randomize Latina participants with elevated genetic and Social Determinants of Heath (SDH) risks. Within 1 week of enrollment, all Latina Aim 1 participants in both study arms will engage in three 30-minute, individual, phone-based sessions with the study team across 3 consecutive weeks

Key facts

Study ID

NCT05483283

Run by

University of Illinois at Chicago

People needed

600

Starts

2023-01-18

Expected to finish

2027-09-01

Last updated by the study team

2026-03-10

Who can join

Age: 30 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Aim 1
• female biological sex
• identification as Latina
• one genetic risk factor (i.e., personal history of breast cancer or family history of breast or ovarian cancer)
• one SDH risk factor, based on the American Cancer Society's definitions (e.g., perceived financial struggles; transportation difficulties; exposure to violence; housing challenges; social isolation/challenges)
• 30+ years old, based on American Cancer Society (ACS) screening guidelines for high risk populations
• No receipt of cancer genetic counseling AND no receipt of genetic testing
• Aim 2
• female biological sex
• referral from Latina Aim 1 participants
• eligibility to obtain BC screenings, based on ACS guidelines (e.g., optional annual
• screenings at 40-44 years old, recommended annual screenings at 45-54 years old, every other year screening at 55 and older)
• self-report not attending Session #3 (as this will not be recorded by the staff)
• Aim 3
• participant from Aim 1 or
• participant from Aim 2

You may not qualify if…

• Aim 1 and Aim 2 Not meeting at least one of the inclusion criteria
• Aim 3
• Not a participant from Aim 1 or
• Not a participant from Aim 2

Where it is running

• University of Illinois — Chicago, Illinois, United States (enrolling)

Full record on ClinicalTrials.gov

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