Patient Experience Data in Radiation Oncology
- Conditions
- PROMsRadiotherapy Side Effect
- Interventions
- Radiation: external beam photon therapy
- Registration Number
- NCT05224297
- Lead Sponsor
- Medical University of Vienna
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 6000
- all patients receiving external beam radiotherapy
- unable to independently answer questionnaires on radiation-induced side effects
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description pelvis male external beam photon therapy - abdomen external beam photon therapy - head and neck external beam photon therapy - thorax external beam photon therapy - pelvis female external beam photon therapy - extremities external beam photon therapy - skin external beam photon therapy - breast external beam photon therapy - skull external beam photon therapy -
- Primary Outcome Measures
Name Time Method radiation-related side effects during radiotherapy and after (up until 5 years)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Medical University of Vienna
🇦🇹Vienna, Austria