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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06118229
Enrollment
300
Registered
2023-11-07
Start date
2023-03-09
Completion date
2026-03-31
Last updated
2024-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Small Cell Lung Cancer

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

DEVICEWearable smart devices and PROs

Patients wearing wearable smart devices to monitor physiological data while regularly utilizing PROs to report subjective assessments of their own health status.

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Postoperative length of hospital stayFrom 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

MeasureTime frameDescription
Operative timeFrom time of the start of surgery to the end of surgeryOperative 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

Contacts

Primary ContactJianxing He, M.D
drjianxing.he@gmail.com+86-20-83337792
Backup ContactWenhua Liang, M.D
liangwh1987@163.com+86-13710249454

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026