Under construction – not a live service
Sign in
Taking people in ItalyNo phase

Mobile Tool to Help Patients With Bladder Cancer Track Quality of Life

Asks adults with urothelial carcinoma which contents they find useful in a web app.

Plain-language title generated from the registry record
Registry title: A Patient-Directed Mobile Tool to Streamline the QoL Assessment and Monitoring in Urothelial Carcinoma

Key facts

Where
Milan, ItalySee the site

Where in Italy

  • IRCCS San RaffaeleMilan, ItalyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
IRCCS San Raffaele
Trial code
NCT06982794
Record updated
21 May 2025
Original description
The goal of this observational study is to select contents and tools for the future development of a web app aiming to support patients' navigation for empowering decision-making through a higher awareness of urothelial carcinoma and its treatments, improving also educational aspects.Read full original descriptionShow less

'UROLIFE': a Patient-Directed Mobile Tool to Streamline the QoL Assessment and Monitoring in Urothelial Carcinoma

The goal of this observational study is to select contents and tools for the future development of a web app aiming to support patients' navigation for empowering decision-making through a higher awareness of urothelial carcinoma and its treatments, improving also educational aspects.

The main question it aims to answer is:

What are the contents that patients diagnosed with urothelial carcinoma find useful to include in a web app to streamline their quality of life assessment and monitoring?

Participants candidate for systemic treatments, or already under treatment, will answer questionnaires about the tools to include in a web app designed for urothelial carcinoma.

Inclusion: histological diagnosis of urothelial carcinoma; ≥ 18 years old,; candidate for systemic treatment with chemotherapy, immune-checkpoint inhibitors, antibody-drug conjugates, or target therapy (patients can be enrolled also if the treatment has started),; possession of a mobile device (e.g., smartphone or personal computer) with the physical and psychological ability to use mobile devices,; understanding and speaking the Italian language,; ability to sign an informed consent.

Exclusion: not possession of a mobile device,; unwillingness to give informed consent.

ClinicalTrials.gov NCT06982794