Promoting Informed Choice for Breast Cancer Screening

NCT05376241 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 637

Last updated 2026-03-27

Study results available
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Summary

Identify the prevalence and predictors of reactance, self-exemption, disbelief, source derogation in reaction to evidence about mammography benefits and harms, and consequences for decision-making and trust.

Conditions

Interventions

BEHAVIORAL

Decision aid

Mammography screening decision aid for women in their 40s with information about screening guidelines, breast cancer mortality reduction, false positives, overdiagnosis, and a personal breast cancer risk estimate.

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • University of Colorado, Denver

    lead OTHER

Principal Investigators

  • Laura Scherer · University of Colorado, Denver

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
39 Years
Max Age
49 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-03
Primary Completion
2022-05-07
Completion
2022-05-07

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT05376241 on ClinicalTrials.gov