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Your journey
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More info
You can access this
clinical trial
if you have
Prostate Cancer, Erectile Dysfunction or Sexual Dysfunction
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

The burden of sexual dysfunction after prostate cancer surgery is responsible for the single greatest impact on patient/partner health-related quality of life; substantially more so than concern for cancer recurrence, or any other post-surgery side-effect. Consequently, there is a great need for progressive and distributable sexual health rehabilitation interventions designed to uphold intimacy and optimal sexual health. If the biomedical-psychosocial intervention is ultimately found beneficial, it will result in: 1) an empirically-based intervention that helps patients/partners maintain optimal health-related quality of life after prostate cancer surgery, and 2) a highly structured protocol and manualized intervention that is translatable to other treatment groups (e.g. radiation therapy) and University/Community-based hospitals.

Provided treatments

  • Behavioral: Biomedical Component
  • Behavioral: Psychosocial Component
  • Behavioral: Attention Control

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02640131. The sponsor of the trial is University Health Network, Toronto and it is looking for 65 volunteers for the current phase.
Official trial title:
A Bio-psychosocial Sexual Health Intervention for Prostate Cancer Survivors and Partners: a Feasibility Study