- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02753985
Adherence to Aromatase Inhibitors: The Role of Partners
July 22, 2019 updated by: Abramson Cancer Center of the University of Pennsylvania
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.
Study Overview
Study Type
Observational
Enrollment (Actual)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104
- Abramson Cancer Center of the University of Pennsylvania
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
Women and partners of women with stage I-III breast cancer
Description
Inclusion Criteria:
Women and partners of women with stage I-III breast cancer who
- have completed primary cancer treatments (surgery, chemotherapy, radiotherapy)
- have experienced AI side effects
live with a romantic partner.
Exclusion Criteria:
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Number of Surveys Completed
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2014
Primary Completion (ACTUAL)
April 22, 2016
Study Completion (ACTUAL)
April 22, 2016
Study Registration Dates
First Submitted
April 26, 2016
First Submitted That Met QC Criteria
April 26, 2016
First Posted (ESTIMATE)
April 28, 2016
Study Record Updates
Last Update Posted (ACTUAL)
July 23, 2019
Last Update Submitted That Met QC Criteria
July 22, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- UPCC 15114
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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