Study Aims
- Elicit key stakeholder input to evaluate the implementation potential of the BREASTChoice tool.
- Optimize BREASTChoice based on stakeholder input and usability testing, and prepare it for implementation.
- Aim 2 Results:
- Evaluate the effects of the updated BREASTChoice in a randomized controlled trial in a diverse population.
Year 1
- Obtain IRB approvals *study preparation*
- Recruit and interview participants (patients, clinicians and Informatics/IT specialists or administrators)
- Make initial tool modifications
- Observe workflows and test usability *Usability testing stage*
Year 2
- Observe workflows and test usability *Usability testing stage*
- Make final tool modifications
- Enroll patients and collect data *Randomized
controlled trial stages*
- Patients will first be approached by phone
- Patients who consent will view one of the websites
- Patients who consent will complete a final questionnaire
Year 3
- Enroll patients and collect data *Randomized controlled trial stages*
- Analyze data
- Share our findings