Study aims to improve shared Decision-Making in metastatic breast cancer
NCT ID NCT03248258
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study from the University of Alabama at Birmingham involved 200 women with metastatic or early-stage breast cancer. Researchers conducted interviews and focus groups with patients, nurses, and doctors to understand how treatment decisions are made, including the option to reduce chemotherapy. The goal was to develop an electronic treatment plan that supports shared decision-making, where patients' values and preferences are considered alongside medical advice.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better communication tools that help patients and doctors make treatment choices together, improving quality of care.
- What could go wrong
- This is a small, qualitative study that does not test a treatment. The findings may not apply to all patients or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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200 people
The number who actually took part.
- Started
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Jun 2017
- Finished
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Dec 2022
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Metastatic and Early stage Breast Cancer patients receiving care at UAB Hematology/Oncology Kirklin Clinic. Breast Cancer Patient advocates, oncology nurses, navigators, and Oncology Physicians
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Patient Criteria (Phase I,II,III): Inclusion Criteria: * 1\. Women with age ≥ 18 * 2\. Presence of Metastatic Breast Cancer or Early Stage Breast Cancer * 3\. Patients may be receiving any line and type of therapy including both standard of care and clinical trials. Exclusion Criteria: * 1\. Patient who are not able to read and/or speak English * 2\. Patients with a life expectancy less than 3 months * 3\. Patients unable to provide informed consent * 4\. Men Patient Advocates (Phase III) Inclusion criteria: 1\. Providers who are self-identified patient advocates working with breast cancer researchers Exclusion criteria: 1. None Sampling: We will conduct interviews with 10-20 patient advocates for phase 3 of this project. Provider (navigator, nurse, physician) (Pjhase I, III) Inclusion criteria: 2. Providers who have direct contact with breast cancer patients Exclusion criteria: 2\. None
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Alabama at Birmingham
Birmingham, Alabama, 35249, United States
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