Dissemination of BREASTChoice AIM1-B
Dissemination of a Breast Reconstruction Decision Tool Through Social Media and Online Communities- AIM1-B
UNC Lineberger Comprehensive Cancer Center
20 participants
Oct 1, 2025
INTERVENTIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria7
- Inclusions Criteria To participate in this study, a subject must meet all the eligibility criteria outlined below.
- Age ≥ 18 years at the time of consent
- Able to read and speak English.
- Have had surgery, such as a mastectomy or lumpectomy, to remove some or all of their breast or breasts.
- Breast surgery occurred within the past 8 years.
- Breast surgery was due to a diagnosis of breast cancer, ductal carcinoma in situ, or risk of future breast cancer, by participant report.
- Sex was assigned "Female" at birth
Exclusion Criteria1
- • Individuals with self-reported or observed unstable medical or psychiatric conditions precluding informed consent or participation in the study will be excluded.
Interventions
Participants will be screened and share demographic information during screening. If eligible and screened in, the interviewer will send the self-administered pre-survey Decision Quality Index (DQI).
Participants will participate in a semi-structured interview and review of the adapted BREASTChoice tool.
Participants will take the post-survey to assess breast reconstruction decision quality.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07396766