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Psychosocial Outcomes and Contralateral Prophylactic Mastectomy (CPM)

NCT02263014 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 345

Last updated 2025-11-26

Study results available
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Summary

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.

Conditions

Interventions

BEHAVIORAL

Questionnaires

Screening questionnaire completed at baseline. Surgery decision questionnaires completed at surgical consult visit, and at 1, 6, 12, and 18 months after the surgery is completed.

Sponsors & Collaborators

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER

  • M.D. Anderson Cancer Center

    lead OTHER

Principal Investigators

  • Abenaa M. Brewster, MD, MHS, BS · M.D. Anderson Cancer Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-02-24
Primary Completion
2016-10-31
Completion
2028-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02263014 on ClinicalTrials.gov