Actively Recruiting
Dissemination of BREASTChoice AIM1-B
Led by UNC Lineberger Comprehensive Cancer Center · Updated on 2026-02-09
20
Participants Needed
1
Research Sites
172 weeks
Total Duration
On this page
Sponsors
U
UNC Lineberger Comprehensive Cancer Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This registration covers only Aim 1b, which focuses on testing usability. The study will include 20 participants who are breast cancer patients. Participants will be observed using the tool on their mobile devices, and their experience will be evaluated using a "think-aloud" method to capture their thoughts and reactions. Interviews will include open-ended questions about the content and format of the decision aid, with follow-up prompts to gather feedback on design elements (length, order, graphics), comprehension, ease of use, acceptance, and engagement with the tool. Knowledge will be measured using the Decision Quality Instrument before and after using the tool. Results will be analyzed to develop recommendations for the final version of the tool.
CONDITIONS
Official Title
Dissemination of BREASTChoice AIM1-B
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age �3E�3D 18 years at the time of consent
- Able to read and speak English
- Have had surgery such as mastectomy or lumpectomy to remove some or all of their breast(s)
- Breast surgery occurred within the past 8 years
- Breast surgery was due to diagnosis of breast cancer, ductal carcinoma in situ, or risk of future breast cancer by participant report
- Sex was assigned "Female" at birth
You will not qualify if you...
- Individuals with unstable medical or psychiatric conditions that prevent informed consent or participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of North Carolina
Chapel Hill, North Carolina, United States, 27599
Actively Recruiting
Research Team
V
Victoria Triana
CONTACT
K
Kathryn A Chetwynd
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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