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NCT06981026Recruiting

The Effectiveness of Telemedicine Monitoring Prehabilitation in Prostate Cancer Patients Undergoing Radical Prostatectomy

Source: ClinicalTrials.gov · Last updated 27 Jul 2026

Brief summary (registry, in English)

The study titled " The effectiveness of telemedicine monitoring prehabilitation in prostate cancer patients undergoing radical prostatectomy " investigates the impact of a structured telemedicine-supported prehabilitation and rehabilitation program on reducing postoperative urinary incontinence in patients with localized prostate cancer. Radical prostatectomy, a common treatment for localized prostate cancer, is often associated with complications such as urinary incontinence, which significantly affects quality of life. This study aims to address this issue by enhancing patients' physical conditioning and adherence to pre- and postoperative rehabilitation through the use of wearable devices and remote physiotherapy consultations.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
18 Mar 2025
Start date
1 Jun 2026
Primary completion date
31 Dec 2027
Lead sponsor
University Hospital Olomouc
NCT number
NCT06981026

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 1 Jun 2026 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.

Prior treatment

  • Prior pelvic radiotherapy or hormone therapy for prostate cancer recurrence.

Other illness

  • Other malignant tumors, except for benign skin carcinoma.
  • Diagnosed mental or cognitive disorders.
  • Severe musculoskeletal disorders preventing active exercise

Other

  • Active treatment for other oncological diagnoses.
  • Presence of preoperative urinary incontinence.
  • Inability to use required technologies

Who the study is looking for

  • Biopsy-confirmed localized prostate cancer (ICD code C.61).
  • Indicated for radical prostatectomy, with or without pelvic lymphadenectomy (ePLND).
  • Not previously treated for prostate cancer, including radiation therapy to the pelvis, major pelvic surgery, or placement of a penile implant or artificial urinary sphincter.
  • No known urethral stricture or colostomy or chronic urinary catheterization.
  • No medical or current psychiatric disorders that precludes their participation in the study.
  • Status of the musculoskeletal system allowing physical exercise.
  • Urinary continent at baseline.
  • Has reliable internet and the skills/knowledge to use technologies use for the study.

Age in the registry: 40 years to 80 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Urology clinic, University hospital Olomouc
Coordinator of this site? Confirm its status
OlomoucCzechiaRecruiting

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