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Feasibility of a Web-based Patient Reported Outcome Symptom Monitoring Application in Danish Lung Cancer Patients

NCT03529851 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-08-29

No results posted yet for this study

Summary

The trial is a pilot study prior to a following phase III trial and is designed to test the feasibility, acceptability and technical usability of supplementary web-based follow-up in lung cancer via a patient-reported outcome application.

Conditions

  • Lung Cancer Stage IV

Interventions

OTHER

Weekly questionnaires

In case of alarming symptoms reported in the questionnaire, an alert is automatically sent to the hospital. The clinicians will contact the patient, confirm the symptoms and intervene according to standard practice.

Sponsors & Collaborators

  • Danish Cancer Society

    collaborator OTHER

  • Danish Lung Cancer Group

    collaborator OTHER

  • Regional Hospital West Jutland

    lead OTHER

Principal Investigators

  • Rasmus Friis, MD · Department of Oncology, Regional Hospital West Jutland

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2018-08-01
Completion
2018-08-01

Countries

  • Denmark

Study Locations

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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 NCT03529851 on ClinicalTrials.gov