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Canada-wide Implementation of a Virtual Sexual Health and Rehabilitation eClinic (SHAReClinic) for Prostate Cancer Patients and Their Partners

Prostate Cancer | Sexual Dysfunction, Physiological | Sexual Dysfunction | Implementation |...

The goal of this observational study is to evaluate the effectiveness of SHAReClinic, a national, virtual Sexual Health and Rehabilitation eClinic designed to support prostate cancer patients and their partners. Specifically, this study aims to assess SHAReClinic's impact on improving sexual function, satisfaction, and relational intimacy after treatment.

The primary objective is to evaluate SHAReClinic's effectiveness across participating sites and determine its role in supporting long-term sexual health and well-being.

As part of usual care, newly enrolled SHAReClinic patients will receive guided education modules and access to sexual health counselling at key recovery milestones.

SHAReClinic seeks to expand access to sexual health care for prostate cancer patients across Canada by providing evidence-based, virtual sexual rehabilitation. Findings from this study will inform best practices in survivorship care and contribute to the development of a national standard for oncology sexual health interventions.

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Participation Requirements

  • Sex:

    MALE
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Patients who are scheduled for first-line treatment for localized prostate cancer, either through radical prostatectomy (open or robotic) or radiation treatment (brachytherapy, external beam) Alone, or with adjuvant Androgen Deprivation Therapy (ADT) OR

* Patients currently undergoing active treatment for prostate cancer OR
* Patients who have undergone cancer treatment in the past 6 months
* Patients who are hormone and/or chemotherapy-naïve
* Patients who have access to a computer or smartphone with internet access
* Patients who are 18 years of age or older

Exclusion Criteria:

* Patients on ADT alone as primary treatment, and/or patients on chemotherapy
* Patients who lack English proficiency
* Patients on nitrate therapy or have other contra-indications to phosphodiesterase type 5 inhibitors (PDE5i's)
* Patients with medical conditions that would preclude safe sexual activity
* Patients who have had previous treatment for PCa

Study Location

Men's Health Clinic Manitoba
Men's Health Clinic Manitoba
Winnipeg, Manitoba
Canada

Contact Study Team

Primary Contact

Avinash Sarcar

[email protected]
204-221-4476
St. Joseph's Health Care London
St. Joseph's Health Care London
London, Ontario
Canada

Contact Study Team

Primary Contact

Mary McKibbon

[email protected]
519-646-6100
St. Paul's Hospital
St. Paul's Hospital
Saskatoon, Saskatchewan
Canada

Contact Study Team

Dianne & Irving Kipnes Urology Centre
Dianne & Irving Kipnes Urology Centre
Edmonton, Ontario
Canada

Contact Study Team

Primary Contact

Sarah Rayner-Myers

[email protected]
825-963-6459
Grass Family Men's Health Center
Grass Family Men's Health Center
Ottawa, Ontario
Canada

Contact Study Team

Primary Contact

Amanda Ross

[email protected]
613-798-5555
Vancouver Coastal Health Authority
Vancouver Coastal Health Authority
Vancouver, British Columbia
Canada

Contact Study Team

Primary Contact

Monita Sundar

[email protected]
(604) 875-4111
Kingston Health Sciences Centre
Kingston Health Sciences Centre
Kingston, Ontario
Canada

Contact Study Team

Primary Contact

Debora Stark

[email protected]
613-544-2631
University Health Network
University Health Network
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Steven Guirguis

[email protected]
416-946-4501
Royal Victoria Regional Health Centre
Royal Victoria Regional Health Centre
Barrie, Ontario
Canada

Contact Study Team

Primary Contact

Lindsey Huff

[email protected]
705-728-9090
Trillium Health Partners
Trillium Health Partners
Mississauga, Ontario
Canada

Contact Study Team

Study Sponsored By
University Health Network, Toronto
Participants Required
More Information
Study ID: NCT06877598