Female Cancer Patients' Preference For Sexual Health Interventions
NCT ID: NCT01084642
Last Updated: 2017-07-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
229 participants
OBSERVATIONAL
2010-03-04
2017-07-03
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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survey
Participants will be asked to complete a survey as a one time assessment.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* 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
* Patients with a psychiatric disorder precluding response to the surveys.
21 Years
FEMALE
No
Sponsors
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Memorial Sloan Kettering Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Jeanne Carter, PhD
Role: PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Locations
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Memorial Sloan Kettering Cancer Center
New York, New York, United States
Countries
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Related Links
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Memorial Sloan Kettering Cancer Center
Other Identifiers
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10-034
Identifier Type: -
Identifier Source: org_study_id
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