Promoting Informed Choice for Breast Cancer Screening: A Longitudinal Study

Completed · Not applicable

Conditions studied: Breast Cancer

In brief

All participants will read a decision aid (DA) communicating evidence about mammography screening benefits and harms. Participants' evaluations of that evidence will be assessed, along with their screening intentions and receipt of screening. Participants will be sent 3 surveys via email and a final brief survey conducted by email or phone. The four surveys will be collected 1) upon enrollment and prior to the primary care appointment; 2) following the primary care appointment; 3) 3 months after enrollment; 4) 1 year after enrollment. The final 2 surveys will offer an increased incentive to increase retention rates.

Key facts

Study ID

NCT05838417

Run by

University of Colorado, Denver

People needed

499

Starts

2022-11-22

Expected to finish

2025-11-30

Last updated by the study team

2026-04-23

Who can join

Age: 39 and older, up to 49. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Individuals who identify as female at birth
• Ages 39-49 years old (inclusive) at the time of consent
• English literacy
• Internet access
• No prior diagnosis of breast cancer, ductal carcinoma in situ (DCIS, also known as "stage zero breast cancer"), or lobular carcinoma in situ
• No known BCRA1/2 gene mutation

You may not qualify if…

• Individuals who identify other than female at birth
• Individuals who are currently pregnant
• Individuals < 39 years old or 50 years old and > at the time of consent
• Lack English literacy
• Lack of internet access
• Prior diagnosis of breast cancer, ductal carcinoma in situ (DCIS, also known as "stage zero breast cancer"), or lobular carcinoma in situ
• Known BCRA1/2 gene mutation
• Decisionally Challenged Individuals
• Prisoners or those on alternative sentencing or probation

Where it is running

• University of Colorado Hospital — Aurora, Colorado, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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