Living Well After Breast Surgery

NCT03834532 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2021-11-02

No results posted yet for this study

Summary

Decision making about whether to have breast reconstruction after mastectomy can be difficult, and previous studies have found that many women are not well informed about their options. Patient decision aids can improve decision quality for a variety of health conditions. This pilot randomized study seeks to determine how a patient decision aid about breast reconstruction affects the quality of decisions about reconstruction including patient knowledge, concordance between preferences and treatment, and decisional regret.

Conditions

  • Breast Cancer Female
  • Stage I Breast Cancer
  • Stage II Breast Cancer
  • Stage III Breast Cancer
  • Ductal Carcinoma in Situ
  • Ductal Breast Carcinoma
  • Lobular Breast Carcinoma

Interventions

OTHER

Breast reconstruction decision aid

The breast reconstruction decision aid is a web-based, interactive tool that participants will use after the first breast surgery visit and before a plastic surgery visit or surgery. The decision aid provides information about post-mastectomy breast reconstruction and helps the participant clarify their preferences related to the procedure.

OTHER

Educational website

The educational website contains information on healthy living with breast cancer including, physical activity and nutrition.

Sponsors & Collaborators

  • Ohio State University

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • University of Texas at Austin

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-18
Primary Completion
2021-06-11
Completion
2021-06-11

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 NCT03834532 on ClinicalTrials.gov