Breast Cancer Clinical Trial
Sexual Health and Rehabilitation After Ovarian Suppression Treatment
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.
Full 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
Eligibility Criteria
Inclusion Criteria:
Women with a history of breast cancer who are currently on chemical ovarian suppression
Current age ≤ 50
No active cancer therapy in the past 6 months and no future therapy planned
Endorsement of at least one sexual symptom (see Appendix A for eligibility screening)
English-speaking
Exclusion Criteria:
History of pelvic radiation
Prior participation in one of Dr. Bober's sexual health workshops
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There is 1 Location for this study
Boston Massachusetts, 02215, United States
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