Goals of Sexual Function in Prostate Cancer Survivors and Their Partners After Cancer Treatment

This study has been completed.
Sponsor:
Information provided by:
Abramson Cancer Center of the University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT01018901
First received: November 23, 2009
Last updated: May 3, 2010
Last verified: May 2010

November 23, 2009
May 3, 2010
January 2009
January 2010   (final data collection date for primary outcome measure)
Goals of sexual functioning [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01018901 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Goals of Sexual Function in Prostate Cancer Survivors and Their Partners After Cancer Treatment
Goals for Sexual Functioning of Prostate Cancer Survivors and Their Partners Following Cancer Treatment

RATIONALE: Gathering information about survivors of prostate cancer and their partners may help doctors learn more about the goals for sexual functioning after cancer treatment. PURPOSE: This clinical trial is studying the goals of sexual functioning in prostate cancer survivors and their partners after cancer treatment.

Detailed DescriptionOBJECTIVES:

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.

Interventional
Not Provided
Intervention Model: Single Group Assignment
Masking: Open Label
Prostate Cancer
Other: Survey Administration
Patients complete survey
Experimental: 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.
Intervention: Other: Survey Administration
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
80
January 2010
January 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Prostate cancer survivors who are: willing and able to provide informed consent; able to read, write, and speak English; married or are in married-like relationship; completed radiation or surgery for their prostate cancer 6 months to 5 years ago
  • Partners of prostate cancer survivors must be: willing and able to provide informed consent; able to read, write, and speak English

Exclusion Criteria:

  • Prostate cancer survivors will be excluded if they have undergone androgen deprivation therapy within the past 6 months and if their partners refuse to participate
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01018901
UPCC 23808
No
James Coyne, Principal Investigator, Abramson Cancer Center of the University of Pennsylvania
Abramson Cancer Center of the University of Pennsylvania
Not Provided
Not Provided
Abramson Cancer Center of the University of Pennsylvania
May 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP