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Development of a Patient Decision Aid for Women Considering Breast Reconstruction

NCT04817709 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 126

Last updated 2021-05-24

No results posted yet for this study

Summary

This study engages cancer survivors who have considered breast reconstruction after mastectomy in developing and pilot testing an up-to-date, understandable, meaningful patient decision aid video and workbook. Once the video and workbook are pilot-tested, a field test with new patients will then compare whether it is more feasible and useful for women considering breast reconstruction after mastectomy to view a video and workbook before their appointment or an educational booklet during their appointment. The video explains the process and types of reconstruction, the timeline for how breast reconstruction is done, and how the cost of this surgery is covered. The workbook helps patients compare your options and prepare for the appointment. The educational booklet explains the same process, types, timeline and costs, and is designed to help the patient and their surgeon compare and discuss the options together during the appointment. By comparing these two methods, researchers may learn which of these is more effective in helping patients make a decision about breast reconstruction.

Conditions

  • Breast Carcinoma

Interventions

OTHER

Educational Intervention

Review workbook

OTHER

Usual Care

Receive educational materials

OTHER

Media Intervention

Watch video

OTHER

Medical Chart Review

Review of medical records

OTHER

Questionnaire Administration

Complete questionnaires

Sponsors & Collaborators

  • M.D. Anderson Cancer Center

    lead OTHER

Principal Investigators

  • Gregory Reece · M.D. Anderson Cancer Center

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-03-20
Primary Completion
2021-05-20
Completion
2021-05-20

Countries

  • United States

Study Locations

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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 NCT04817709 on ClinicalTrials.gov