NCT07693647Enrolling by invitation
Evaluation of Pelvic Floor Function and Psychosocial Sequelae Following Radical Prostatectomy for Prostate Cancer
Evaluation of Urinary Incontinence, Erectile Dysfunction, and Psychosocial Outcomes Following Radical Prostatectomy for Prostate Cancer
Source: ClinicalTrials.gov · Last updated 13 Jul 2026
Brief summary (registry, in English)
This observational cross-sectional study aims to evaluate the effects of radical prostatectomy for prostate cancer on pelvic floor function and psychosocial well-being. The study will assess the prevalence and severity of urinary incontinence and erectile dysfunction, as well as their impact on quality of life, sexual health, self-esteem, and interpersonal relationships. Adult men who underwent radical prostatectomy at least one year before enrollment will complete a series of validated questionnaires and provide demographic and clinical information through online surveys or telephone interviews. The study will also explore whether participants received pelvic floor physiotherapy before or after surgery and whether rehabilitation is associated with better functional and psychosocial outcomes. The findings may contribute to a better understanding of the long-term consequences of radical prostatectomy and help identify opportunities to improve patient care.
- Status (registry)
- Enrolling by invitation
- Study type
- Observational
- Enrollment
- 67 (estimated)
- First submitted
- 2 Jul 2026
- Start date
- 1 Jan 2025
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- University of Valencia
- Diseases
- Prostate cancer
- NCT number
- NCT07693647
What you commit to
- Study type: Observational
- Planned participants: 67
- From 1 Jan 2025 to the primary completion date, 31 Dec 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Presence of comorbidities that may independently contribute to urinary incontinence or erectile dysfunction (e.g., neurological disorders or other relevant medical conditions).
- Severe cognitive or sensory impairment that prevents understanding the study procedures or completing the questionnaires.
Other
- Refusal or inability to provide informed consent.
Who the study is looking for
- Male participants aged 18 years or older. History of radical prostatectomy for prostate cancer, regardless of the surgical technique used.
- At least 12 months since radical prostatectomy. Able to understand the study information and provide electronic informed consent.
- Able to complete the questionnaires in Spanish, either independently or with the support of a structured telephone interview.
- Willing to participate voluntarily in the study.
Age in the registry: 18 years to - · Sex: Male · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Gascó Oliag, 5 Coordinator of this site? Confirm its status | Valencia | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.