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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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4 February 2013 |
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Main ID: |
NCT01084642 |
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Date of registration:
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09/03/2010 |
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Primary sponsor: |
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Public title:
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Female Cancer Patients' Preference For Sexual Health Interventions
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Scientific title:
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A Pilot Study Surveying Female Cancer Patients' Preference For Sexual Health Interventions |
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Date of first enrolment:
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March 2010 |
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Target sample size:
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300 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01084642 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Countries of recruitment
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United States
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Contacts
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Name:
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Jeanne Carter, PhD |
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Address:
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Telephone:
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646-888-5076 |
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Email:
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Affiliation:
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Name:
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Jeanne Carter, PhD |
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Address:
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Telephone:
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646-888-5076 |
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Email:
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Affiliation:
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Name:
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Jeanne Carter, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Memorial Sloan-Kettering Cancer Center |
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Key inclusion & exclusion criteria
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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.
Age minimum:
21 Years
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Breast Cancer
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Gynecologic Cancer
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Primary Outcome(s)
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Participant' awareness of sexual health issues & preference for sexual health intervention
[Time Frame: 2 years]
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Secondary Outcome(s)
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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]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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