Trial Information
Inclusion Criteria:
- Men who have been treated for localized prostate cancer
- AND men must be 6-36 months post-prostatectomy or radiation (as primary treatment) of
prostate cancer
- Must have a heterosexual, co-cohabiting partner who is willing to participate
- Must speak and read English
- Must be able to use a computer and have internet access
Exclusion Criteria:
- Homosexual couples will not be included in this study
- Major self-reported psychiatric illness
- Couples who screen below 30 on the DAS (Dyadic Adjustment Scale)
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Outcome Measure:
Change in Sexual Function from Baseline to 13 weeks
Outcome Time Frame:
Pre-Intervention (Week 1); Post-Intervention (Week 7); 3 Months Post-Intervention (Week 13)
Safety Issue:
No
Principal Investigator
Deborah L McLeod, R.N., Ph.D.
Investigator Role:
Principal Investigator
Investigator Affiliation:
Capital District Health Authority & Dalhousie University
Authority:
Canada: Capital District Health Authority REB
Study ID:
CDHA-RS/2013-076
NCT ID:
NCT01716702
Start Date:
November 2012
Completion Date:
January 2014
Related Keywords:
- Prostate Cancer
- Prostate Cancer
- Psychosocial Intervention
- Sexual Rehabilitation
- Online Intervention
- Prostatic Neoplasms