Trial Information
Intervention to Improve Self-Care of Symptoms in Breast Cancer Survivors on Adjuvant Endocrine Therapy.
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.
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care
Outcome Measure:
Satisfaction determined by the Client Satisfaction Survey
Outcome Time Frame:
Up to 6 months.
Safety Issue:
No
Principal Investigator
G van Londen, MD, MS
Investigator Role:
Principal Investigator
Investigator Affiliation:
University of Pittsburgh
Authority:
United States: Institutional Review Board
Study ID:
PRO12050094
NCT ID:
NCT01738685
Start Date:
December 2012
Completion Date:
December 2015
Related Keywords:
- Breast Cancer.
- Breast Cancer.
- Adjuvant Endocrine therapy.
- Breast Neoplasms
Name | Location |
University of Pittsburgh |
Pittsburgh, Pennsylvania 15261 |