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

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

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01738685
Acronym
Relief
Enrollment
0
Registered
2012-11-30
Start date
2012-12-31
Completion date
2015-12-31
Last updated
2016-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Female

Keywords

Breast Cancer., Adjuvant Endocrine therapy.

Brief 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.

Interventions

BEHAVIORALBehavioral Intervention.
OTHERNutritional Education.

Sponsors

University of Pittsburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
50 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Satisfaction determined by the Client Satisfaction SurveyUp to 6 months.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026