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Clinical Trial Summary

The central goal of this study is to examine the feasibility, acceptability, and preliminary efficacy of the IE intervention on patient and partner sexual QOL and relationship outcomes, and on patient psychosocial outcomes. We expect that the IE will show adequate feasibility, acceptability, and preliminary efficacy. Secondarily, based on the rationale that barriers exist that limit participation in intensive sexual QOL interventions for breast cancer survivors, an innovative secondary aim will investigate the perspectives of study-eligible patient candidates who opt out of participating in the pilot trial. We expect that we will be able to identify the participation barriers and intervention preferences of breast cancer survivors with sexual concerns who opt out of the intensive trial in order to inform the development of different interventions for future study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02721147
Study type Interventional
Source Fox Chase Cancer Center
Contact
Status Completed
Phase N/A
Start date October 27, 2015
Completion date September 29, 2017

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