Goals of Sexual Function in Prostate Cancer Survivors and Their Partners After Cancer Treatment
NCT ID: NCT01018901
Last Updated: 2020-04-09
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
NA
2 participants
INTERVENTIONAL
2009-01-31
2013-12-31
Brief Summary
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Detailed Description
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I. To collect data on the goals of sexual functioning among prostate cancer survivors and their partners following cancer treatment in order to identify specific components of interventions for future grant submissions on the psychosexual needs of prostate cancer survivors.
OUTLINE:
Patients and their partners complete surveys. Sexual function of men is assessed by the International Index of Erectile Function; sexual function of women is assessed by the Female Sexual Function Index.
Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Arm I
Patients and their partners complete surveys. Sexual function of men is assessed by the International Index of Erectile Function; sexual function of women is assessed by the Female Sexual Function Index.
Survey Administration
Patients complete survey
Interventions
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Survey Administration
Patients complete survey
Eligibility Criteria
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Inclusion Criteria
* Partners of prostate cancer survivors must be: willing and able to provide informed consent; able to read, write, and speak English
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Abramson Cancer Center at Penn Medicine
OTHER
Responsible Party
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Principal Investigators
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James Coyne, PhD
Role: PRINCIPAL_INVESTIGATOR
Abramson Cancer Center at Penn Medicine
Locations
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Abramson Cancer Center of the University of Pennsylvania
Philadelphia, Pennsylvania, United States
Countries
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Other Identifiers
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UPCC 23808
Identifier Type: -
Identifier Source: org_study_id
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