Dana Farber Cancer Institute
Boston, Massachusetts, 02215, United States
NCT Number: NCT03447886
The overall goal of this study is to qualitatively explore how behavioral, cultural, psychosocial, and economic barriers and facilitators affect the decision to start and adhere to endocrine therapy (ET) among young breast cancer survivors of diverse racial, ethnic, and socio-economic backgrounds with hormone receptor positive (HR+) breast cancer
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Notify Me18 year–45 year
Female
Observational
Boston, Massachusetts, 02215, United States
A qualitative study that will use interviews to gain an in depth understanding of factors affecting the decision to start and adhere to endocrine therapy (ET) among young breast cancer survivors of diverse racial, ethnic, and socio-economic backgrounds with hormone receptor positive (HR+) breast cancer
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Collecting clinical and socio-demographic information.
Time frame: 3 months-3 years post active treatment
Open ended questions
Time frame: 3 months-3 years post active treatment
Open ended questions
Time frame: 3 months-3 years post active treatment
Open ended questions
Time frame: 3 months-3 years post active treatment
Open ended questions
Time frame: 3 months-3 years post active treatment
Open ended questions
Time frame: 3 months-3 years post active treatment
Brief Health Literacy Screener (Chew items)
Time frame: 3 months-3 years post active treatment
BCPT Symptom Checklist
Dana-Farber Cancer Institute
Other
Understanding Barriers to Initiation and Adherence to Adjuvant Endocrine Therapy in Young Breast Cancer Survivors of Diverse Racial, Ethnic, and Socio-economic Backgrounds: The EMPOWER Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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