A Study to Explore the Role and Impact of Wearable Smart Devices in Perioperative NSCLC Patients

Guangzhou Medical University

Status: Enrolling

Conditions: Non Small Cell Lung Cancer

Treatments: Device: Wearable smart devices and PROs

Study type: Observational

Funder types: Other

Identifiers

NCT06118229

WISP-NSCLC

Details and patient eligibility

About

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.

Enrollment: 300 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

300 participants in 1 patient group

NSCLC patients wearing wearable smart devices

Description:

NSCLC patients wearing wearable smart devices while utilizing PROs for regular follow-up

Treatment:

Device: Wearable smart devices and PROs