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Recruiting NCT06275126

NCT06275126 Optimizing Surgical Decisions in Young Adults With Breast Cancer

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Clinical Trial Summary
NCT ID NCT06275126
Status Recruiting
Phase
Sponsor Weill Medical College of Cornell University
Condition Breast Cancer Stage 0
Study Type INTERVENTIONAL
Enrollment 800 participants
Start Date 2024-03-13
Primary Completion 2027-05-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 44 Years
Study Type INTERVENTIONAL
Interventions
CONSYDER decision aid

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 800 participants in total. It began in 2024-03-13 with a primary completion date of 2027-05-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Female aged 18-44 * New diagnosis of Stage 0, 1, 2, or 3 unilateral breast cancer * English or Spanish speaking Exclusion Criteria: * Diagnosis of de novo Stage 4 breast cancer * Recurrent early-stage breast cancer * Bilateral breast cancer

Contact & Investigator

Central Contact

Shoshana Rosenberg, ScD, MPH

✉ shr4009@med.cornell.edu

📞 646-962-8041

Principal Investigator

Shoshana Rosenberg, ScD, MPH

PRINCIPAL INVESTIGATOR

Weill Medical College of Cornell University

Frequently Asked Questions

Who can join the NCT06275126 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 44 Years, studying Breast Cancer Stage 0. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06275126 currently recruiting?

Yes, NCT06275126 is actively recruiting participants. Contact the research team at shr4009@med.cornell.edu for enrollment information.

Where is the NCT06275126 trial being conducted?

This trial is being conducted at New Haven, United States, Boston, United States, New York, United States, Durham, United States.

Who is sponsoring the NCT06275126 clinical trial?

NCT06275126 is sponsored by Weill Medical College of Cornell University. The principal investigator is Shoshana Rosenberg, ScD, MPH at Weill Medical College of Cornell University. The trial plans to enroll 800 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology