Preoperative Physical Activity Improvement With the Use of Activity Trackers Before Radical Cystectomy (PreAct) — PreAct  

Bladder Cancer Clinical Trial

Official title: Preoperative Physical Activity Improvement With the Use of Activity Trackers in Patients Undergoing Radical Cystectomy for Bladder Cancer: A Randomized Controlled Trial (PreAct)

Status Recruiting

Clinical Trial Summary

A bicentric, open-label randomised controlled trial (RCT) is planned to investigate whether the use of fitness wristbands in a defined preoperative period prior to radical cystectomy leads to a preoperative increase in participants' physical activity (number of steps per day) up to the day of radical cystectomy.

Clinical Trial Description

The goal of the PreAct study is to test whether the use of fitness wristbands in a defined preoperative period prior to radical cystectomy with a daily activity goal and feedback on the achievement of this goal improves the participants' physical activity up to the day of radical cystectomy.

In addition to the fitness tracker, we provide each patient with a smartphone. For each fitness tracker a separate account in a fitness application is set up for (e.g. name: tracker1.0 with the corresponding e-mail address and password). Neither the patients in the Daily activity Goal and Feedback arm nor the No Daily Activity Goal or Feedback arm receive the access data to the accounts. However, the patients in the intervention group receive the access PIN for the smartphone. On this smartphone a messaging service and the fitness application are installed. The patient thus receives, for example the wristband tracker1.0, which is registered with the corresponding access data in the fitness application of the smartphone given to them. For the entire preoperative period, the Bluetooth function on the smartphone must always stay activated so that the fitness application and the fitness tracker are continuously connected to each other. A detailed description of the timing and implementation of the intervention are described in "Study design" and "Arm and Interventions". ;

Related Conditions & MeSH terms

• Bladder Cancer
• Bladder Neoplasm
• Bladder Urothelial Carcinoma
• Urinary Bladder Neoplasms

• NCT number: NCT06416319
• Study type: Interventional
• Source: Universitätsmedizin Mannheim
• Contact: Karl-Friedrich Kowalewski, PD Dr. med.
• Phone: 0152-53404943
• Email: karl-friedrich.kowalewski@umm.de
• Status: Recruiting
• Phase: N/A
• Start date: March 14, 2023
• Completion date: March 14, 2026