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ChatGPT & Surgeon Synergy: Redefining Breast Reconstruction Consultations for Enhanced Patient Engagement and Satisfaction

ChatGPT & Surgeon Synergy: Redefining Breast Reconstruction Consultations for Enhanced Patient Engagement and Satisfaction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06981208
Enrollment
410
Registered
2025-05-20
Start date
2025-06-03
Completion date
2028-06-30
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Cancer of the Breast

Keywords

Patient education, ChatGPT, Breast reconstruction

Brief 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.

Interventions

OTHERChatGPT-generated patient education

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.

OTHERUsual patient education

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.

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Caregiver)

Masking description

The surgeons will be blinded to the patient's randomization arm prior to the in-person consultation.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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.

Design outcomes

Primary

MeasureTime frameDescription
Patient perceived understanding of breast reconstructionPre-surgical consultation (day 1)The patient will choose an answer ranging from 0-100 (strongly disagree to strongly agree). The higher the score, the more perceived understanding the patient had.

Secondary

MeasureTime frameDescription
Patient satisfaction with education regarding breast reconstructionPre-surgical consultation (day 1)The patient will choose an answer ranging from 0-100 (strongly disagree to strongly agree). The higher the score, the more satisfied the patient was.
Surgeon satisfaction with the consultation processPre-surgical consultation (day 1)Survey includes two question regarding surgeon's satisfaction with the consultation process. The surgeon will choose an answer ranging from 0-100 (strongly disagree to strongly agree). The higher the score, the more satisfied the surgeon was with the consultation process.
Surgeon perception of patient preparednessPre-surgical consultation (day 1)Survey includes one question regarding patient preparedness. The surgeon will choose an answer ranging from 0-100 (strongly disagree to strongly agree). The higher the score, the more prepared the surgeon felt the patient was.
Surgeon views on the efficiency of the consultationPre-surgical consultation (day 1)Survey includes one question regarding efficiency of the consultation. The surgeon will choose an answer ranging from 0-100 (strongly disagree to strongly agree). The higher the score, the more efficient the surgeon felt the consult was.
Surgeon overall experience with the consultationPre-surgical consultation (day 1)Survey includes one question regarding the pre-surgical consultation overall experience. The surgeon will choose an answer ranging from 0-100 (strongly disagree to strongly agree). The higher the score, the better the overall experience was.

Countries

United States

Contacts

CONTACTSaif M Badran, M.D., Ph.D., FRCS
badran@wustl.edu314-273-1434
PRINCIPAL_INVESTIGATORSaif M Badran, M.D., Ph.D., FRCS

Washington University School of Medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026