CTRI/2023/10/058202
Recruiting
未知
Evaluating the Use of Patient-Reported Outcome Measures for Improving the Inter-RaterReliability of Common Terminology Criteria for Adverse Event Ratings - nil
European Organisation for Research and Treatment of Cancer0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- European Organisation for Research and Treatment of Cancer
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.The study population will be adult cancer patients fulfilling the following inclusion criteria: patients
- •aged above 18\.
- •2\.Any cancer diagnosis (no more than 20% per diagnostic group) current treatment with chemotherapy or immunotherapy inpatient or day clinic setting
- •3\.Scoring 3 or above on an initial screening question (On a scale of 0 to 10, to what degree did you experience physical or emotional symptoms/problems during the last week? ?).
- •4\.No severe cognitive impairments written informed consent.
- •Inclusion criteria for physicians performing CTCAE ratings will be at least one year of professional experience in oncology. Chemotherapy has been selected because the EORTC QLQ\-C30 covers common AEs associated with this treatment. Immunotherapy has been added for being an increasingly important treatment option.
Exclusion Criteria
- •There are no exclusion criteria for this study. All types of cancer patients will be enrolled on the study.
Outcomes
Primary Outcomes
Not specified
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