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Clinical Trial Summary

This research study is evaluating an educational intervention for breast cancer survivors who have experienced changes in sexual function after ovarian suppression treatment to reduce the risk of breast cancer recurrence.


Clinical Trial Description

The purpose of this research is to study the effectiveness of an educational intervention for breast cancer survivors who have experienced changes in sexual function after ovarian suppression treatment to reduce the risk of cancer recurrence. The aim is to develop an effective intervention to help women manage these changes and restore sexual health and functioning. - This study consists of attending a group educational session followed by a one-on-one telephone coaching session. - The group educational session will last about 4 hours, and will include information on resources, self-help strategies, and relaxation techniques. - The telephone coaching session will take place four weeks after the group session, and will last about 15 minutes ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03571841
Study type Interventional
Source Dana-Farber Cancer Institute
Contact
Status Completed
Phase N/A
Start date December 1, 2018
Completion date December 1, 2019

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