Tumor
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age >= 18 years; 2.Histologically or cytologically confirmed solid malignant tumor; 3.Scheduled to receive initial radical or adjuvant external beam radiotherapy; 4.Conscious and competent, without severe cognitive or mental disorders, capable of understanding and completing the questionnaire; 5.Voluntary participation with signed written informed consent.
Exclusion criteria
Exclusion criteria: 1.Prior history of cranial radiotherapy or presence of confirmed brain metastases (to avoid confounding effects of direct central nervous system involvement on fatigue assessment); 2.Severe non-malignant comorbidities expected to cause severe fatigue per se or significantly interfere with assessment (e.g., New York Heart Association Class IV heart failure, severe chronic obstructive pulmonary disease, etc.); 3.Currently enrolled in other interventional clinical trials with fatigue as the primary endpoint; 4.Any other conditions deemed by the investigators as unsuitable for participation in this study; 5.Cognitive impairment, language communication barriers, or psychiatric disorders that preclude understanding and completion of questionnaire assessment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The anticipated incidence of moderate-to-severe cancer-related fatigue (defined as RPFS score >= 4 points) in this trial; | — |
Secondary
| Measure | Time frame |
|---|---|
| Age and gender; | — |
Countries
China
Contacts
The Second Affiliated Hospital of Air Force Medical University, Chinese People's Liberation Army