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A Pilot Study Surveying Female Cancer Patients' Preference For Sexual Health Interventions


N/A
21 Years
N/A
Open (Enrolling)
Female
Breast Cancer, Gynecologic Cancer

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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 CenterNew York, New York  10021