An observational, non-interventional cohort study to monitor physical and social activity of bladder cancer patients during treatment with curative intent by using conventional and digital methodology

An observational, non-interventional cohort study to monitor physical and social activity of bladder cancer patients during treatment with curative intent by using conventional and digital methodology - Digital monitoring of bladder cancer patients (eBladder)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON51316

Enrollment

Registered

2023-01-31

Start date

2023-03-22

Completion date

Unknown

Last updated

2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder cancer

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Able to provide written informed consent. 2. Patients suspected of or with pathologically confirmed diagnosis of bladder cancer, with as predominant type urothelial carcinoma or squamous cell carcinoma. a. Before or after undergoing TURBT. b. Before starting the rest of their treatment. 3. >= 18 years at screening. 4. Has the ability to communicate well in Dutch with the investigator and willing to comply with the study instructions.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

Measure	Time frame
• Smartwatch wear-time • Compliance rates • Adverse device effects	—

Secondary

Measure	Time frame
• Parameters collected from Trial@home • EORTC QLQ-C30 questionnaire • Performance status score	—

Countries

Netherlands

Outcome results