Patient Experience Data in Radiation Oncology

Recruiting now

Conditions studied: Radiotherapy Side Effect, PROMs

In brief

The project is part of the overarching goal of improving patient-centric radiation oncology. This pilot project aims to develop an instrument that can be used to collect clinically relevant patient-reported outcome data on adverse effects during and after RT. This real-world evidence (RWE) database will be the basis to monitor and evaluate future technological developments, combination treatments (e.g. radioimmunotherapy, etc.), or changes in treatment protocols. The pseudonymized data will be linked to data in the oncological information system and dosimetric data from the treatment planning system. In this way, they represent a basic building block of patient-oriented development of clinical radiotherapy.

Key facts

Study ID

NCT05224297

Run by

Medical University of Vienna

People needed

6000

Starts

2020-10-01

Expected to finish

2025-01-01

Last updated by the study team

2024-11-22

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• all patients receiving external beam radiotherapy

You may not qualify if…

• unable to independently answer questionnaires on radiation-induced side effects

Where it is running

• Medical University of Vienna — Vienna, State of Vienna, Austria (enrolling)

Full record on ClinicalTrials.gov

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