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NCT07335354
A Study of a Decision Tool for People Considering Breast Reconstruction Surgery
Conditions: Breast Cancer
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 131
Sponsor: Memorial Sloan Kettering Cancer Center
Location: Memorial Sloan Kettering Basking Ridge Basking Ridge New Jersey
Summary
The purpose of this study is to find out whether it is practical (feasible) to do a larger study looking at the effectiveness of the Breast Reconstruction Decision Aid Tool (RECONJOINT) for breast reconstruction surgery.
Eligibility Criteria
Participant Inclusion Criteria
Focus Group Participants
* A diagnosed genetic predisposition to breast cancer or a diagnosis of ductal carcinoma in situ or any invasive cancer confirmed through review of the medical record
* ≥18 years old
* Considering post-mastectomy breast reconstruction
RCT Participants (Patients)
* A diagnosed genetic predisposition to breast cancer or a diagnosis of ductal carcinoma in situ or any invasive cancer confirmed through review of the medical record
* ≥18 years old
* Considering post-mastectomy breast reconstruction
* Have an appointment scheduled for consultation with a plastic surgery provider
RCT Participants (Physicians)
* Provides breast reconstruction care ≥ 50% of the time. This is defined as over half of the surgeon's cases in the preceding calendar year being related to breast reconstruction surgery.
Participant Exclusion Criteria
Focus Group Participants
* Not considering post-mastectomy breast reconstruction
* Non-English proficiency
RCT Participants (Patients)
* Not considering postmastectomy breast reconstruction
* Recurrent or metastatic breast cancer
* Male sex
* Non-English proficiency
RCT Participants (Physicians)
* Does not provide breast reconstruction care at least 50% of the time
* Non-English proficiency
Source: ClinicalTrials.gov (NCT07335354). StuddyBuddy aggregates publicly available trial information.