Decision Support for Women With Breast Cancer
Stopped early · Not applicable
Conditions studied: Breast Neoplasms
In brief
Breast cancer is a common malignancy among women in the United States. There are a variety of treatment decisions that need to be made. This study has been developed after a review of the literature demonstrated that women with breast cancer are making decisions regarding complex therapy issues in a way that is not congruent with their decision-making control preference. Some patients want to be empowered with information so that they can actively participate in the decision making about their care; others want to rely on the recommendations made by the oncologist. This is important because patients who were not satisfied with their adjuvant treatment decision noted a negative effect on quality of life and self image. These patients had more difficulties with treatment side effects; including aches, hot flashes, pain, and mood alteration. In additions the Institute of Medicine recommended that patient centeredness be a key aim of health care organizations and that all patients be given the opportunity to exercise the degree of control they choose over health care decisions that affect them. It is hypothesized that women making decisions regarding adjuvant therapy who are supported to make decisions based on their preferred level of control will have positive psychological outcomes.
Key facts
- Study ID
- NCT01447771
- Run by
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- People needed
- 14
- Starts
- 2011-09-01
- Expected to finish
- 2012-03-01
- Last updated by the study team
- 2014-04-09
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women with early stage (Stage I and Stage II) breast cancer that are considering adjuvant therapy and are being evaluated at the Johns Hopkins Avon Foundation Breast Center.
- Age 18 years and older.
- Able to read and speak English.
You may not qualify if…
- Severe visual impairments that would make it difficult to read study instruments or inability to read.
- Lack of capacity to provide informed consent to participate in the study.
- Patients being seen for a second opinion.
- Patients with a history of previous neoadjuvant chemotherapy.
- Women who are pregnant.
Where it is running
- Johns Hopkins Hospital — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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