ChatGPT & Surgeon Synergy: Redefining Breast Reconstruction Consultations for Enhanced Patient Engagement and Satisfaction
Washington University School of Medicine
410 participants
Jun 3, 2025
INTERVENTIONAL
Conditions
Summary
In this study, patients who are scheduled for breast reconstruction consultation will be randomized into the intervention group (ChatGPT-generated patient education regarding possible reconstruction options) or the control group (usual patient education). All patients will complete a survey following their in-person consultation to assess their experience and overall satisfaction with the consultation process. Additionally, participating surgeons will complete a separate survey to evaluate their consultation experience, satisfaction, and to assess the accuracy and clinical utility of the ChatGPT-generated patient education materials. The surveys are designed to gather information on patient characteristics, organizational health literacy according to Brega et al. Other survey questions have been designed to meet the outcomes of this study and have not been based on previously published surveys.
Eligibility
Inclusion Criteria9
- Patient Eligibility Criteria:
- Scheduled for initial preoperative breast reconstruction consultation following therapeutic or prophylactic mastectomy with a surgeon at Washington University School of Medicine.
- At least 18 years of age.
- Can speak and understand English.
- Surgeon Eligibility Criteria:
- Routinely performs breast reconstruction surgery at Washington University School of Medicine.
- At least 18 years of age.
- Can speak and understand English.
- Surgeon must not be a resident or fellow at time of enrollment.
Interventions
This is created by entering the patient's age, medical history, social history, and case-specific details into Washington University ChatGPT Beta (HIPAA and FERPA compliant) by a study team member.
Usual patient education will include description of breast reconstruction options, with further elaboration on which option are more suitable to the patient. This include also review of risk of complications and expected recovery after surgery.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06981208