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Communicating Objective Risk for Personalized Decision Making About Mammography

NCT01686360 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1560

Last updated 2017-07-21

No results posted yet for this study

Summary

The purpose of this study is to test the effects of objective risk information about breast cancer and mammography outcomes using a randomized control trial. Women between the ages of 35 and 49 will receive information about their personal risk for breast cancer and be randomly assigned to receive data about a woman who should be screened, data about the potential outcomes of screening, or data about breast cancer deaths. Two presentation formats will be tested and compared.

Conditions

Interventions

BEHAVIORAL

Decision Aid

Sponsors & Collaborators

Principal Investigators

  • Joseph N Cappella, PhD · University of Pennsylvania

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
35 Years
Max Age
49 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2012-12-18
Completion
2012-12-18

Countries

  • United States

Study Locations

More Related Trials

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 NCT01686360 on ClinicalTrials.gov