Actively Recruiting
Preoperative Physical Activity Before Radical Cystectomy and the Impact on Morbidity
Led by Ludwig-Maximilians - University of Munich · Updated on 2026-04-27
146
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Bladder cancer (BC) is the 6th most common tumor in Europe, with over 540,000 new cases globally each year. While 75% of cases are non-muscle-invasive and treated bladder-preservingly, muscle-invasive, non-metastatic BC requires radical cystectomy (RC), often with neoadjuvant chemotherapy. RC has one of the highest complication rates in urology, and rehabilitation focuses on mitigating functional impairments, restoring physical and mental capacity, and enabling a swift return to daily life. The ERAS (Enhanced Recovery After Surgery) protocol has shown benefits in reducing hospital stays without increasing complications in RC. Prehabilitation studies in cancer patients have demonstrated improvements in strength and fitness, though without significant reductions in complications or mortality. This prospective randomized study, conducted over three years at the University of Munich, will evaluate the effect of preoperative physical activity on perioperative morbidity (primary endpoint). Secondary endpoints include quality of life, hospital stay, mortality, and postoperative physical activity. The intervention group will target 8,000-10,000 daily steps for four weeks preoperatively, monitored via pedometers. Follow-ups will assess physical activity and quality of life at specific intervals pre- and post-surgery.
CONDITIONS
Official Title
Preoperative Physical Activity Before Radical Cystectomy and the Impact on Morbidity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Urothelial cell cancer of the bladder
- Planned treatment with radical cystectomy
You will not qualify if you...
- Need for walking aid
- Depression
- Cardiovascular, neuromuscular, or orthopedic deficits or disorders
- Time to surgery less than 3 weeks
AI-Screening
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Trial Site Locations
Total: 1 location
1
Department of Urology, LMU Hospital
Munich, Bavaria, Germany, 81377
Actively Recruiting
Research Team
Y
Yannic Volz, PD Dr. med.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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