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Behavioral and Psychological Impact of Returning Breast Density Results to Latinas

NCT02910986 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1386

Last updated 2025-08-28

Study results available
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Summary

This study will examine behavioral and psychological outcomes of breast density notification using a 3-group randomized design comparing usual written notification to two educationally enhanced approaches.

Conditions

Interventions

BEHAVIORAL

Written educational brochure

Written educational brochure about breast density

BEHAVIORAL

Promotora interaction

Promotora education about breast density

Sponsors & Collaborators

  • Mountain Park Health Center

    collaborator UNKNOWN

  • National Institute on Minority Health and Health Disparities (NIMHD)

    collaborator NIH

  • Mayo Clinic

    lead OTHER

Principal Investigators

  • Celine M. Vachon, Ph.D. · Mayo Clinic

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
74 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-10-27
Primary Completion
2019-11-15
Completion
2019-11-15

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02910986 on ClinicalTrials.gov