Acute pain and pulmonary function decline after thoracoscopic lung resection for pulmonary nodules and primary lung cancer.
Conditions
Interventions
Intervention group:Routine care combined with standardized VR rehabilitation intervention
Sponsors
Fuzhou University Affiliated Provincial Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Patients aged 18 to 75 years. 2.Patients scheduled for elective thoracoscopic lobectomy, segmentectomy, or wedge resection. 3.Patients with American Society of Anesthesiologists (ASA) physical status classification I–III. 4.Patients with normal consciousness and communication ability who are able to complete pain assessment, pulmonary function evaluation, and rehabilitation training. 5.Patients voluntarily participating in this study and signing written informed consent.
Exclusion criteria
Exclusion criteria: 1.Patients with vertigo, motion sickness, epilepsy, severe eye disease, or other conditions that may cause intolerance to VR equipment. 2.Patients with severe cardiopulmonary insufficiency, cognitive impairment, psychiatric disorders, or inability to communicate effectively before surgery. 3.Pregnant or lactating women. 4.Patients who underwent intraoperative conversion to thoracotomy or developed severe postoperative complications requiring intensive care unit treatment. 5.Patients with long-term opioid use or a history of chronic chest pain before surgery. 6.Other conditions considered unsuitable for participation in this study by the investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NRS pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Early postoperative pulmonary function parameters; | — |
Countries
China
Contacts
Public ContactXing Lin
Fuzhou University Affiliated Provincial Hospital
Outcome results
None listed