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Clinical Trials/NCT06745401
NCT06745401
Completed
N/A

Remote Monitoring of Cancer Patients With Outpatient Treatment

Persei Vivarium1 site in 1 country34 target enrollmentNovember 21, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Persei Vivarium
Enrollment
34
Locations
1
Primary Endpoint
Usability of Caaring® for the management of oncology patients in outpatient oral treatment
Status
Completed
Last Updated
11 months ago

Overview

Brief Summary

This project focuses on studying the use of digital platforms for monitoring, between medical visits, parameters such as toxicities and therapeutic adherence.

The goal of this observational study is to know the degree of usability of the Caaring® digital platform in cancer patients undergoing outpatient oral treatment. This will allow in the future to design comparative studies that demonstrate the advantages of using this application in the management of these patients.

Participants will fill out various questionnaires in the Caaring app related to their symptoms, adherence to treatment, quality of life and physical activity, among others.

Registry
clinicaltrials.gov
Start Date
November 21, 2024
End Date
March 3, 2025
Last Updated
11 months ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Persei Vivarium
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Cancer patients with adjuvant or metastatic oncological treatment
  • Cancer patients with oral oncological treatment
  • Patients who are able to complete the study questionnaires
  • Patients who are able to handle the application on a smart mobile phone.
  • Informed consent is obtained from the patient.

Exclusion Criteria

  • Patients who will not be able to commit to carrying out the follow-ups or do not have adequate technological skills.
  • Patients with inability to give adequately the informed consent.

Outcomes

Primary Outcomes

Usability of Caaring® for the management of oncology patients in outpatient oral treatment

Time Frame: Day 0 up to 3 months

Percentage of patients with at least 80% of the data completed in the application, Percentage of patients with 100% of the data completed in the application and Percentage of completion per patient

Secondary Outcomes

  • Degree of completion of data relating to treatment adherence(Weekly up to 3 months)
  • Degree of completion of data related to the toxicity of their treatment(Weekly up to 3 months)
  • Quality of the care process through impact on the patient's quality of life: WHOQOL(Day 0 and week 12)
  • Quality of the care process through impact on the patient's quality of life: IPAQ(Day 0 and week 12)
  • Patient workload(Week 12)

Study Sites (1)

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