Actively Recruiting

Age: 18Years - 100Years
All Genders
ID05224297

Patient Experience Data in Radiation Oncology

Led by Medical University of Vienna · Updated on 2024-11-22

6000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on improving patient-centered care in radiation oncology by developing a tool to collect patient-reported data on side effects experienced during and after radiotherapy. The goal is to create a real-world evidence database that helps monitor and assess future advances in radiation treatments, combination therapies, and protocol changes. The collected data will be linked anonymously to clinical and dosimetric information to support patient-oriented development in radiotherapy. Participants receive external beam photon therapy targeting various tumor locations such as breast, thorax, skin, abdomen, skull, head and neck, pelvis (male and female), and extremities. The study gathers information on radiation-related side effects during radiotherapy and up to five years afterward, enabling long-term monitoring of treatment impact. During the study, participants will be asked to complete questionnaires reporting any side effects they experience. These patient-reported outcomes will be combined with clinical and treatment data for comprehensive analysis. The study is observational, with no experimental treatments, and participants' usual care will continue throughout. The total involvement may last up to five years for side effect monitoring.

CONDITIONS

Brief Title

Patient Experience Data in Radiation Oncology

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All patients receiving external beam radiotherapy
  • Aged 18 to 100 years
  • Able to independently answer questionnaires on radiation-induced side effects
Not Eligible

You will not qualify if you...

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

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - Varies according to treatment plan

Participants receive external beam photon therapy for their specific tumor location.

Long-term Monitoring

Duration - Up to 5 years after treatment

Participants are monitored for radiation-related side effects during radiotherapy and for up to 5 years after treatment.

Trial Site Locations

Total: 1 location

1

Medical University of Vienna

Vienna, State of Vienna, Austria, 1090

Actively Recruiting

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Research Team

G

Gerd Heilemann, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

9

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