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NCT02753985 Clinical Trial

Adherence to Aromatase Inhibitors: The Role of Partners

Breast Cancer Survivors Clinical Trial

Official title:
Adherence to Aromatase Inhibitors: The Role of Partners

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02753985
Other study ID # UPCC 15114
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2014
Est. completion date April 22, 2016

Study information
Verified date July 2019
Source Abramson Cancer Center of the University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a qualitative study which explores the role that partners play in breast cancer survivors adherence to aromatase inhibitors and management of their side effects. Both patients and their partners will be interviewed (separately) in order to capture multiple perspectives. The target number of subjects is 64 (32 patients and 32 partners). The primary method of data collection will be face-to-face semi-structured interviews. These interviews will be audio-recorded.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date April 22, 2016
Est. primary completion date April 22, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women and partners of women with stage I-III breast cancer who

1. have completed primary cancer treatments (surgery, chemotherapy, radiotherapy)

2. have experienced AI side effects

3. live with a romantic partner.

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Survey

Locations
Country Name City State
United States Abramson Cancer Center of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
Abramson Cancer Center of the University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Surveys Completed 2 years
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