Psychosocial Outcomes and Contralateral Prophylactic Mastectomy (CPM)

Running, not enrolling

Conditions studied: Breast Cancer

In brief

The goal of this research study is to learn more about how different treatment decisions may influence the quality of life in women with breast cancer. Researchers want to use what is learned from this study to help future patients with breast cancer to be more informed when making treatment decisions.

Key facts

Study ID

NCT02263014

Run by

M.D. Anderson Cancer Center

People needed

345

Starts

2014-02-24

Expected to finish

2028-04-30

Last updated by the study team

2026-06-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Newly diagnosed ductal carcinoma in situ (DCIS) or Stage I-III sporadic unilateral invasive breast cancer
• Age 18 or older
• Able to speak, read, and write English.
• Spouse/Partner: Married or living with patient for a year or more
• Spouse/Partner: Age 18 or older
• Spouse/Partner: Able to speak, read, and write English

You may not qualify if…

• Patients with previous breast cancer
• Prior history of prophylactic mastectomy
• Known to have a germline gene mutation that predisposes them to an increased risk of breast cancer (e.g., BRCA1, BRCA2), and/or if they are considered at high risk for contralateral breast cancer on the basis of a strong family history of cancer

Where it is running

• Kelsey-Seybold — Houston, Texas, United States
• University of Texas MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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