Study Aims and Timeline

Study aims

Aim 1:

Elicit key stakeholder input to evaluate the implementation potential of the BREASTChoice tool.

• Aim 1 results

Aim 2:

Optimize BREASTChoice based on stakeholder input and usability testing, and prepare it for implementation.

• Aim 2 results:
  • Usability testing results
  • EHR integration process lessons learned

Aim 3:

Evaluate the effects of the updated BREASTChoice in a randomized controlled trial in a diverse population.

• Aim 3 results

Study timeline

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 on 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