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OpenTrials
Completed

NCT Number: NCT01084642

Female Cancer Patients' Preference For Sexual Health Interventions

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.

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Key information

Conditions

Breast Cancer Breast Diseases Breast Neoplasms Gynecologic Cancer Neoplasms Neoplasms by Site Skin Diseases Skin and Connective Tissue Diseases

Age range

21 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Memorial Sloan Kettering Cancer Center

New York, 10065, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Participant' awareness of sexual health issues & preference for sexual health intervention

    Time frame: 2 years

Secondary outcomes

  1. To assess & describe female cancer patients' attitudes towards & preference of methods to receive sexual health information (verbal or written) & psychosexual education patient information cards or intervention modality (telephone, in-person or online).

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Memorial Sloan Kettering Cancer Center

Other

Registry information

Official study title

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

Important dates

Study start
2010
Primary completion
2017
Study completion
2017
First posted
Mar 10, 2010
Registry last updated
Jul 6, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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