Optimizing Surgical Decisions in Young Adults With Breast Cancer
Recruiting now · Not applicable
Conditions studied: Breast Cancer Stage 0, Breast Cancer Stage I, Breast Cancer Stage II, Breast Cancer Stage III
In brief
The goal of this study is to understand and improve the breast surgical decision-making process for young women newly diagnosed with breast cancer. As part of this study, the investigators will evaluate the impact and use a web-based tool called CONSYDER that is designed to provide useful information to young breast cancer patients. It is also meant to improve communication between young women and their surgeons with the purpose of helping patients make appropriate surgical decisions. Participants will complete surveys approximately within 1 week of the surgical consult and approximately 6 months after surgery. Patients who receive neoadjuvant chemotherapy will also be surveyed after the completion of neoadjuvant treatment but prior to surgery. Some patients will be invited for an interview after their surgery as part of the evaluation. A subset of patients/surgeons will also have their surgical consultation audio-recorded.
Key facts
- Study ID
- NCT06275126
- Run by
- Weill Medical College of Cornell University
- People needed
- 800
- Starts
- 2024-03-13
- Expected to finish
- 2027-08-31
- Last updated by the study team
- 2025-09-09
Who can join
Age: 18 and older, up to 44. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female aged 18-44
- New diagnosis of Stage 0, 1, 2, or 3 unilateral breast cancer
- English or Spanish speaking
You may not qualify if…
- Diagnosis of de novo Stage 4 breast cancer
- Recurrent early-stage breast cancer
- Bilateral breast cancer
Where it is running
- Yale Cancer Center — New Haven, Connecticut, United States (enrolling)
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States (enrolling)
- Weill Cornell Medicine — New York, New York, United States (enrolling)
- Duke Cancer Institute — Durham, North Carolina, United States (enrolling)
Full record on ClinicalTrials.gov
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