A Home-Based Prehabilitation Exercise Intervention for Improving Physical Function in Patients With Bladder Cancer and Upper Tract Urothelial Cancer, Get Moving Trial
NCT06040762 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128
Last updated 2026-03-02
Summary
Prehabilitation refers to the process of improving a patient's functional capabilities prior to a surgical procedure with the goal of decreasing post-surgical inactivity and physical decline. This clinical trial evaluates the utility of a personalized home-based prehabilitation exercise intervention for the improvement of physical function and surgical outcomes in patients with urothelial carcinoma undergoing definitive or consolidative surgery of the bladder (radical cystectomy) or upper tract (nephroureterectomy, ureterectomy) with or without preceding neoadjuvant/systemic therapy. The exercise intervention includes at-home exercise sessions focused on the improvement of core strength and balance as well as personalized step count goals, delivered to patients remotely via a smart-device-based application (ExerciseRx). Encouraging physical activity before surgery may improve physical function and surgical outcomes in patients who are scheduled to undergo surgery for their bladder or urothelial cancer.
Conditions
- Bladder Cancer
- Urothelial Carcinoma
- Upper Tract Urothelial Carcinoma
- Renal Pelvis and Ureter Urothelial Carcinoma
Interventions
- OTHER
-
Best Practice
Receive SOC educational materials
- OTHER
-
Exercise Intervention
Receive (P)REHAB exercise program
- OTHER
-
App-Based Intervention
Use ExerciseRx app
- OTHER
-
App-Based Intervention
Use FitBit app
- OTHER
-
Interview
Ancillary studies
- OTHER
-
Wearable Activity Tracker
Wear FitBit
- OTHER
-
Physical Performance Testing
Ancillary studies
- OTHER
-
Questionnaire Administration
Ancillary studies
Sponsors & Collaborators
-
Bladder Cancer Advocacy Network
collaborator OTHER - lead OTHER
Principal Investigators
-
Sarah Psutka · Fred Hutch/University of Washington Cancer Consortium
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-12-19
- Primary Completion
- 2027-04-30
- Completion
- 2027-04-30
Countries
- United States
Study Locations
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