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Routine Electronic Patient-reported Outcome Measures During and After Radiotherapy: A Randomized Controlled Study

NCT06598293 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 536

Last updated 2024-09-27

No results posted yet for this study

Summary

Patients in this study will be asked to periodically self-report their symptoms using their smartphones during the radiotherapy period and during the acute phase (3 months) after treatment, and radiation oncology physicians will evaluate the impact on cancer patients' quality of life and determine whether they can improve health outcomes by using this data in their practice.

Conditions

Interventions

BEHAVIORAL

PRO-CTCAE, Pain NRS

The Common Terminology Criteria for Adverse Events (PRO-CTCAE) is a PROM developed to systematically and objectively reflect patients' experiences and perceptions of therapeutic drugs in toxicity evaluation and adverse event reporting. PRO-CTCAE can be used to monitor patients' symptoms and side effects, support therapeutic decision-making, facilitate communication among medical staff, implement patient-centred care, and screen for health conditions.

Sponsors & Collaborators

  • Yonsei University

    lead OTHER

Principal Investigators

  • Hwakyung BYUN, Phd · Severance Hospital

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-03
Primary Completion
2027-07-30
Completion
2028-02-28

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

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 NCT06598293 on ClinicalTrials.gov