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Recruiting NCT06780176

A Study of Breast Cancer Risk Factors and Outcomes of People in Florida

Observational Breast Cancer Breast Neoplasms Breast Diseases

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Biospecimen Collection, Surgical Tissue Collection, Survey Collection.
Who it may be relevant to
Registry conditions: Breast Cancer, Breast Neoplasms, Breast Diseases. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Genomic and Non-Genomic Factors Associated With Breast Cancer Risk Factors and Outcomes in a Diverse South Florida Population

Overview

The purpose of this study is to understand why different people have different risks and outcomes for breast cancer and non-breast cancer.

Interventions

  • Other Biospecimen Collection
    Blood collection at baseline and time of surgery
  • Diagnostic test Surgical Tissue Collection
    Tissue collection will be attempted at time of surgery
  • Behavioral Survey Collection
    Survey collection at baseline, post-surgery, at 1, 3 and 5 year follow up visits

Primary outcome measures

  • Clinical characteristic of participants (survey) [Time frame: Up to 5 years]

Eligibility criteria

Inclusion criteria

  • Patients with BIRADS 0-5, seen in breast radiology clinic at University of Miami (UM), Sylvester Comprehensive Cancer Center (SCCC), Jackson Health Systems (JHS) for biopsy.
  • Any new breast patient seen at UM/SCCC or JHS will be invited to participate in the study.
  • Men and women 18 years of age and older are eligible to participate in the study.

Exclusion criteria

  • Patients who are less than 18 years of age will be considered ineligible.
  • Patients unable to complete the survey.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

United States · 3 centers
  • University of California, Los Angeles (Specimen Analysis only) — Los Angeles
  • University of Miami (Data Collection Only) — Miami
  • Memorial Sloan Kettering Cancer Center (All protocol activites) — New York

Identifiers

NCT: NCT06780176 · 24-372

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗