Breast Cancer Clinical Trial

Intervention to Improve Self-Care of Symptoms in Breast Cancer Survivors on Adjuvant Endocrine Therapy

Summary

Hormone responsive breast cancer is common and costly. Long-term adjuvant endocrine therapy (AET) improves breast cancer outcomes greatly, but, unfortunately, is commonly associated with physical and emotional concerns. I propose to evaluate the feasibility and preliminary effectiveness of a behavioral intervention to facilitate problem identification, provide education, coaching for breast cancer survivors with symptoms while on AET. Therefore, the intervention intends to empower women to engage in better self-care and seek out resources they need, which, in turn, will lead to better symptom management.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Age ≥ 50.
Nonmetastatic bread cancer survivors reporting being bothered by 1 or more symptoms related to their treatment with AET (for > 0 months and < 6 months).
Possess a household or cell telephone.
Ability to provide informed consent.

Exclusion Criteria:

Clinically significant cognitive impairment.
Communication barrier limiting ability to participate in telephone assessments.

Study is for people with:

Breast Cancer

Study ID:

NCT01738685

Recruitment Status:

Withdrawn

Sponsor:

University of Pittsburgh

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There is 1 Location for this study

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University of Pittsburgh
Pittsburgh Pennsylvania, 15232, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT01738685

Recruitment Status:

Withdrawn

Sponsor:


University of Pittsburgh

How clear is this clinincal trial information?

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