Non-small cell lung cancer, NSCLC
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Aged >=18 years and <=85 years. 2) Diagnosed with primary non-small cell lung cancer (NSCLC) confirmed by histopathology, and having completed elective radical lobectomy or segmentectomy. 3) Scheduled for discharge between postoperative days 2 and 7, with the investigator judging the patient’s condition to be stable and suitable for participation in this clinical study. 4) Able to operate smartphone applications and wearable devices independently or with the assistance of a caregiver. 5) Voluntarily agrees to participate in the study and has signed a written informed consent form.
Exclusion criteria
Exclusion criteria: 1) Long-term home oxygen therapy prior to surgery, or the presence of severe resting respiratory dysfunction, or coexisting severe cardiopulmonary diseases. 2) Coexisting severe, uncontrolled cardiovascular or cerebrovascular diseases, hepatic insufficiency, or renal insufficiency. 3) Presence of other diseases that severely affect motor function or compliance. 4) Known or suspected history of contact allergy to the medical adhesive or materials used in the wearable devices. 5) Any other condition considered by the investigator to be unsuitable for participation in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| FEV1/FVC;Between-group differences in lung function at 30 days versus three months after surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| The six-minute walk test;Pulmonary function;Perioperative indicators;Feedback from patients;Compliance with the platform; | — |
Countries
China
Contacts
West China Hospital of Sichuan University