Pilot Study of the eHealth Application "Cancer Patients Better Life Experience" (CAPABLE) - Italy

NCT06161233 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2024-03-08

No results posted yet for this study

Summary

The purpose of the CAPABLE study is to compare health-related quality of life in renal cell carcinoma patients who use or do not use a mobile-based application to monitor adverse events for cancer treatment at home. As secondary objectives, the study investigates the usability of the system and its generalizability to other cancer types

Conditions

Interventions

DEVICE

CAPABLE cohort

The CAPABLE cohort receives the mobileapplication and a multi-sensorial smartwatch (ASUS VivoWatch 5 HC-B05). Patients will be asked to use the system for at least 6 months. The CAPABLE app serves three main functionalities for the patient: symptom monitoring, information needs fulfilment and interventions to improve mental- and physical wellbeing

Sponsors & Collaborators

  • University of Pavia

    collaborator OTHER
  • Policlinico di Bari Ospedale Giovanni Paolo XXIII

    collaborator UNKNOWN
  • Biomeris srl

    collaborator UNKNOWN
  • The Netherlands Cancer Institute NKI

    collaborator UNKNOWN
  • University of Haifa

    collaborator OTHER
  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    collaborator OTHER
  • IBM Research

    collaborator UNKNOWN
  • Bitsens JSC

    collaborator UNKNOWN
  • Poznań University of Technology

    collaborator UNKNOWN
  • Deontics LTD

    collaborator UNKNOWN
  • Associazione Italiana Malati di Cancro AIMAC

    collaborator UNKNOWN
  • Universidad Politecnica de Madrid

    collaborator OTHER
  • Istituti Clinici Scientifici Maugeri SpA

    lead OTHER

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-16
Primary Completion
2024-01-31
Completion
2024-01-31

Countries

  • Italy

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06161233 on ClinicalTrials.gov