Non-small cell lung cancer
Conditions
Interventions
Intervention group:Complex intervention program for perioperative symptom clusters
Control group:Routine care
Sponsors
Anhui Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1 Patients newly diagnosed with primary non-small cell lung cancer (NSCLC) at the thoracic surgery outpatient clinic and scheduled for thoracoscopic surgery; 2 Age >= 18 years; 3 Fully aware of their condition and cancer diagnosis; 4 Possess adequate comprehension and verbal communication skills and consent to participate in this study.
Exclusion criteria
Exclusion criteria: 1 Postoperative pathological diagnosis of benign lung tumors or inflammatory lesions; 2 Presence of psychiatric disorders or impaired consciousness; 3 Hematological dysfunction, severe infection, or immune system diseases; 4 History of lobectomy, segmentectomy, or unilateral pneumonectomy; 5 Concurrent other malignant tumors; 6 Karnofsky Performance Status (KPS) score <= 60; 7 Received neoadjuvant radiotherapy, chemotherapy, or immunotherapy prior to surgery, or enrolled in other interventional studies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| symptom cluster;quality of life;functional status;cytokine;critisol; | — |
Secondary
| Measure | Time frame |
|---|---|
| Perception of stress;hope; | — |
Countries
China
Contacts
Public ContactSong Yongxia; Ge Xiaoling
Anhui Medical University
Outcome results
None listed