Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Optimizing Surgical Decisions in Young Adults With Breast Cancer

NCT06275126 · View on ClinicalTrials.gov ↗

Study 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.

Interventions

  • OTHER CONSYDER decision aid

Study Locations (4)

Connecticut

  • Yale Cancer Center — New Haven

Massachusetts

  • Dana-Farber Cancer Institute — Boston

New York

  • Weill Cornell Medicine — New York

North Carolina

  • Duke Cancer Institute — Durham

Trial Details

FieldValue
Enrollment Target 800 participants
Start Date 2024-03-13
Est. Completion 2027-08-31
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06275126

The ClinicalTrials.gov registry entry for NCT06275126 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 679 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Breast Cancer Stage II appearing as the primary indexed condition, and to 1 intervention — of which CONSYDER decision aid is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06275126 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Connecticut, Massachusetts, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06275126 about?

NCT06275126 is a clinical study titled "Optimizing Surgical Decisions in Young Adults With Breast Cancer". 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 informatio...

What is the current status of trial NCT06275126?

This trial is currently recruiting. It is a NA study. The enrollment target is 800 participants. The study started on 2024-03-13. Estimated completion is 2027-08-31.

What conditions does trial NCT06275126 study?

This clinical trial studies the following conditions: Breast Cancer Stage II, Breast Cancer Stage III, Breast Cancer Stage I, Breast Cancer Stage 0. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06275126?

The interventions under investigation include: CONSYDER decision aid (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06275126?

This trial is sponsored by Weill Medical College of Cornell University, which has 679 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06275126 being conducted?

This trial has 4 study locations across Connecticut, Massachusetts, New York, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial