Breast Cancer Clinical Trial

Female Cancer Patients’ Preference For Sexual Health Interventions

Summary

The purpose of this study is to survey female cancer patients' awareness of and preference for methods to improve sexual health. This information will help to improve our understanding of the needs and preferences for sexual health strategies and interventions of our female patients.

The findings of this survey will also be used to develop feasible sexual health resources for our patients and enhance the success of grant proposals to support future sexual health interventions at MSKCC.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Participants must be able to communicate in English to complete the tests.
Study group of breast and/or gynecological cancer survivors.
History of Primary diagnosis of breast and/or gynecological cancer
At least 21 years of age.
In the judgement of the consenting professional able to provide informed consent
In the judgement of the consenting professional, able to communicate well enough in English through verbal and written communication to complete the study assessments.

Exclusion Criteria:

In the judgement of the consenting professional, the individual is able to provide informed consent.
Patients with a psychiatric disorder precluding response to the surveys.

Study is for people with:

Breast Cancer

Estimated Enrollment:

229

Study ID:

NCT01084642

Recruitment Status:

Completed

Sponsor:

Memorial Sloan Kettering Cancer Center

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There is 1 Location for this study

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Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

229

Study ID:

NCT01084642

Recruitment Status:

Completed

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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