Patient Experience Data in Radiation Oncology

NCT ID: NCT05224297

Last Updated: 2024-11-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

6000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-10-01

Study Completion Date

2025-01-01

Brief Summary

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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

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Conditions

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Radiotherapy Side Effect PROMs

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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breast

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

thorax

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

skin

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

abdomen

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

skull

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

head and neck

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

pelvis male

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

pelvis female

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

extremities

external beam photon therapy

Intervention Type RADIATION

Patients receive external beam photon therapy for different tumor locations (groups).

Interventions

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external beam photon therapy

Patients receive external beam photon therapy for different tumor locations (groups).

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* all patients receiving external beam radiotherapy

Exclusion Criteria

* unable to independently answer questionnaires on radiation-induced side effects
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medical University of Vienna

OTHER

Sponsor Role lead

Responsible Party

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Gerd Heilemann

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medical University of Vienna

Vienna, Vienna, Austria

Site Status RECRUITING

Countries

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Austria

Central Contacts

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Gerd Heilemann, PhD

Role: CONTACT

004314040072710

Facility Contacts

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Gerd Heilemann, PhD

Role: primary

Andreas Renner, PhD

Role: backup

Other Identifiers

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2184/2019

Identifier Type: -

Identifier Source: org_study_id

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