Non Small Cell Lung Cancer
Conditions
Keywords
Non Small Cell Lung Cancer, Wearable Devices
Brief summary
The trial was designed as a single-center non-interventional prospective observational study to explore the role and impact of wearable smart devices in perioperative NSCLC patients.
Interventions
Patients wearing wearable smart devices to monitor physiological data while regularly utilizing PROs to report subjective assessments of their own health status.
Sponsors
Study design
Eligibility
Inclusion criteria
1. Participants must provide voluntary consent to participate in this research and possess the capacity to sign an informed consent form. 2. Participants must be aged over 18 years. 3. Participants must have undergone pulmonary resection surgery with a postoperative pathological confirmation of primary lung cancer.
Exclusion criteria
1. Patient refusal to participate in this research. 2. Inability to wear wearable smart monitoring devices due to various reasons. 3. The pathological report suggests a non-small cell lung cancer (NSCLC) exclusion. 4. History of secondary lung cancer surgery.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Postoperative length of hospital stay | From time of surgery to time of discharge from the hospital (assessed up to 30 days) | Postoperative Length of Stay (LOS) refers to the duration of a patient's hospitalization following surgery, typically measured from the completion of the surgical procedure to the time of patient discharge. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Operative time | From time of the start of surgery to the end of surgery | Operative time is defined as the time from the start of the surgical procedure to its completion, including anesthesia induction, surgical incision, manipulation of tissues, closure, and completion of all surgical tasks. |
Countries
China