Treatment for Breast Cancer

Phase-Based Estimates
Mayo Clinic in Arizona, Scottsdale, AZ
Eligible conditions
Breast Cancer

Study Summary

Latinas Learning About Density

See full description

Treatment Effectiveness

Study Objectives

This trial is evaluating whether Treatment will improve 3 primary outcomes, 1 secondary outcome, and 1 other outcome in patients with Breast Cancer. Measurement will happen over the course of Change from baseline anxiety at 1 year.

Year 1
Adherence to mammography screening
Intervention cost
Month 1
Anxiety Short Term
Year 1
Anxiety Longer Term
Month 1
Breast density knowledge

Trial Safety

Trial Design

2 Treatment Groups


This trial requires 1386 total participants across 2 different treatment groups

This trial involves 2 different treatments. Treatment is the primary treatment being studied. Participants will all receive the same treatment. There is no placebo group. The treatments being tested are not being studied for commercial purposes.

InterpersonalUsual Care plus Enhanced plus interaction with a promotora (lay health educator)
Usual Care plus a written educational brochure

Trial Logistics

Trial Timeline

Approximate Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: 1 year post density notification
This trial has the following approximate timeline: 3 weeks for initial screening, variable treatment timelines, and roughly 1 year post density notification for reporting.

Who is running the study

Principal Investigator
C. M. V.
Celine M. Vachon, Principle Investigator
Mayo Clinic

Closest Location

Mayo Clinic in Arizona - Scottsdale, AZ

Eligibility Criteria

This trial is for female patients aged 18 and older. There are 3 eligibility criteria to participate in this trial as listed below.

Mark “yes” if the following statements are true for you:
Attending screening mammography at Mountain Park Health Center
Speak English or Spanish

Patient Q&A Section

Ask a question about the study

Other questions from users

Please Note: These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any geographic restrictions to consider when applying for this trial?

Patients from any state can participate in this trial, so long as they are able to attend all treatment sessions.

Will my insurance cover participating in this trial?

In order to understand how insurance coverage works for this trial, you will need to contact the study coordinator.

See if you qualify for this trial
Get access to this novel treatment for Breast Cancer by sharing your contact details with the study coordinator.