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

RECRUITING NA

SDM POSSIBLE: A Breast Cancer Treatment Decision Aid for Women 70+ With Low-Risk Stage I Breast Cancers

NCT06896474 · View on ClinicalTrials.gov ↗

Study Summary

Investigators aim to conduct a type 1 hybrid effectiveness-implementation surgeon-level cluster randomized clinical trial (RCT) of a multi-level intervention, a shared decision making training for surgeons plus patient decision aid vs. usual care (UC), at 7 large health systems across the U.S. to learn the intervention's effectiveness. Decision aids will be mailed and sent via patient portal and/or via email (when portal/email addresses are available) to patients before their first surgical encounter. The central hypothesis is that the novel intervention will be a key resource to support shared decision making leading to higher quality treatment decisions and as result improved care and outcomes.

Conditions Studied

Interventions

  • BEHAVIORAL Shared Decision-Making Training and Decision Aid

Study Locations (11)

Massachusetts

  • Beth Israel Deaconess Medical Center — Boston
  • Brigham and Women's Hospital — Boston
  • Dana Farber Cancer Institute — Boston
  • Lahey Hospital and Medical Center — Burlington
  • Beth Israel Deaconess Hospital — Needham
  • Dana-Farber/Brigham and Women's Cancer Center at South Shore Hospital — Weymouth

California

  • Beckman Research Institute of the City of Hope — Los Angeles

New Jersey

  • Rutgers State University of New Jersey Medical School — Newark

New Mexico

  • University of New Mexico — Albuquerque

New York

  • University of Rochester — Rochester

North Carolina

  • Duke University — Durham

Trial Details

FieldValue
Enrollment Target 402 participants
Start Date 2026-02-04
Est. Completion 2033-09-30
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06896474

The ClinicalTrials.gov registry entry for NCT06896474 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 402 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beth Israel Deaconess Medical Center, which has 434 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 1 intervention — of which Shared Decision-Making Training and 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: NCT06896474 reports 11 study locations spanning 6 distinct geographic areas — top geographies include Massachusetts, California, New Jersey. 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 NCT06896474 about?

NCT06896474 is a clinical study titled "SDM POSSIBLE: A Breast Cancer Treatment Decision Aid for Women 70+ With Low-Risk Stage I Breast Cancers". Investigators aim to conduct a type 1 hybrid effectiveness-implementation surgeon-level cluster randomized clinical trial (RCT) of a multi-level intervention, a shared decision making training for surgeons plus patient decision aid vs. usual care (UC), at 7 large health systems across the U.S. to le...

What is the current status of trial NCT06896474?

This trial is currently recruiting. It is a NA study. The enrollment target is 402 participants. The study started on 2026-02-04. Estimated completion is 2033-09-30.

What conditions does trial NCT06896474 study?

This clinical trial studies the following conditions: Breast Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06896474?

The interventions under investigation include: Shared Decision-Making Training and Decision Aid (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06896474?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 434 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06896474 being conducted?

This trial has 11 study locations across California, Massachusetts, New Jersey, New Mexico, New York. 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