Trial Information
A Pilot Study Surveying Female Cancer Patients' Preference For Sexual Health Interventions
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.
Type of Study:
Observational
Study Design:
Observational Model: Cohort, Time Perspective: Prospective
Outcome Measure:
Participant' awareness of sexual health issues & preference for sexual health intervention
Outcome Time Frame:
2 years
Safety Issue:
No
Principal Investigator
Jeanne Carter, PhD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Memorial Sloan-Kettering Cancer Center
Authority:
United States: Institutional Review Board
Study ID:
10-034
NCT ID:
NCT01084642
Start Date:
March 2010
Completion Date:
March 2014
Related Keywords:
- Breast Cancer
- Gynecologic Cancer
- Survey
- Sexual Health Issues
- 10-034
- Breast Neoplasms
Name | Location |
Memorial Sloan Kettering Cancer Center |
New York, New York 10021 |