Digital monitoring of bladder cancer patients (eBladder)
- Conditions
- Bladder cancerCancer
- Registration Number
- ISRCTN55744047
- Lead Sponsor
- Amsterdam University Medical Centers
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 50
1. Able to provide written informed consent
2. Patients suspected of or with a pathologically confirmed diagnosis of bladder cancer, with a predominant type of urothelial carcinoma or squamous cell carcinoma
2.1. Before or after undergoing TURBT
2.1. Before starting the rest of their treatment
3. = 18 years at screening
4. Can communicate well in Dutch with the investigator and willing to comply with the study instructions
1. Permanent and temporary alterations on the wrist, including tattoos
2. Inability to wear or use wearables and other digital devices
3. Inability or limitations to walk or move at screening, or use of walking aids
4. History of allergy to surgical steel
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method