Status:

COMPLETED

Electronic Symptom Follow-up of Cancer Patients

Lead Sponsor:

Oulu University Hospital

Conditions:

Cancer

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

Use of ePROs in oncological care have resulted in improvement of QoL, decreased ER visits, and improvement of overall survival. Furthermore, ePRO follow-up resulted in better QoL, improved ECOG status...

Eligibility Criteria

Inclusion

  • Written informed consent prior to any study procedure
  • Advanced breast, lung, colorectal, or pancreatic cancer
  • New cancer medical treatment, chemotherapy or targeted therapy initiated within -/+ 2 weeks from signed consent
  • Age ≥18y
  • ECOG 0-2
  • CRC cohort: Patients with adjuvant treatment, or first or second line of treatment for metastatic disease
  • Patient compliant with study procedures

Exclusion

  • Initiation of new cancer medical treatment \> 2 wks from signed consent
  • Any medical condition that the Investigator considers significant to compromise the safety of the patient or that impairs the interpretation of study assessments
  • No internet access/email

Key Trial Info

Start Date :

January 1 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 31 2022

Estimated Enrollment :

43 Patients enrolled

Trial Details

Trial ID

NCT04081558

Start Date

January 1 2018

End Date

May 31 2022

Last Update

August 29 2025

Active Locations (2)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (2 locations)

1

Oulu University Hospital

Oulu, Finland

2

Vaasa Central Hospital

Vaasa, Finland

Electronic Symptom Follow-up of Cancer Patients | DecenTrialz