Actively Recruiting

Phase Not Applicable
Age: 30Years +
FEMALE
NCT05483283

Empowering Vulnerable and Resilient Latinas to Obtain Breast Cancer Care

Led by University of Illinois at Chicago · Updated on 2026-03-10

600

Participants Needed

1

Research Sites

241 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Empowering Vulnerable and Resilient Latinas to Obtain Breast Cancer Care

Who Can Participate

Age: 30Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female biological sex
  • Identification as Latina
  • At least one genetic risk factor: personal history of breast cancer or family history of breast or ovarian cancer
  • At least one social determinant of health risk factor such as financial struggles, transportation difficulties, exposure to violence, housing challenges, or social isolation
  • Age 30 years or older
  • No prior receipt of cancer genetic counseling or genetic testing
  • For Aim 2: Referral from Latina Aim 1 participants and eligibility for breast cancer screenings based on American Cancer Society guidelines
  • For Aim 2: Self-report of not attending Session #3
  • For Aim 3: Participation in Aim 1 or Aim 2
Not Eligible

You will not qualify if you...

  • Not meeting at least one inclusion criterion for Aim 1 or Aim 2
  • For Aim 3: Not a participant in Aim 1 or Aim 2

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Illinois

Chicago, Illinois, United States, 60612

Actively Recruiting

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Research Team

Y

Yamile Molina, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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