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NCT05608746Active, not recruiting

Prehabilitation in Prostate Cancer Patients, TelePrehabTrial

Prehabilitation in Prostate Cancer Patients Undergoing Nerve Sparring Robot Assisted Radical Prostatectomy.

Source: ClinicalTrials.gov · Last updated 6 Apr 2025

Brief summary (registry, in English)

Localized prostate cancer is commonly treated with radical prostatectomy (RP). Following surgery adverse effects such as urinary incontinence, erectile dysfunction associated with decreased quality of life and decreased physical function are common. Traditionally, interventions to reduce these adverse effects are introduced postoperatively. However, a growing body of literature shows the benefit of interventions prior to surgery to enhance treatment success, known as prehabilitation. Hence, the main purpose of this study is to develop and investigate the feasibility of prehabilitation using telehealth, to implement several interventions prior to elective RP.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
25 Oct 2022
Start date
8 Nov 2022
Primary completion date
Jun 2025
Lead sponsor
University of Aarhus
NCT number
NCT05608746

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 8 Nov 2022 to the primary completion date, Jun 2025
  • 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

  • Severe comorbidities that would prevent the patient from exercising, e.g. recent fractures, severe heart disease or neurological disorders.

Other

  • No possibility to use a smartphone or tablet.

Who the study is looking for

  • Male \> 18 years
  • Diagnosed with prostate cancer and referred to robot assisted nerve sparring RP
  • Adequacy in written and spoken Danish
  • Cognitively well-functioning
  • Able to understand the study procedures and willing to provide signed informed consent

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Regional Hospital Goedstrup
Coordinator of this site? Confirm its status
HerningDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.