A Study to Explore the Role and Impact of Wearable Smart Devices in Perioperative NSCLC Patients
NCT ID: NCT06118229
Last Updated: 2024-06-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
300 participants
OBSERVATIONAL
2023-03-09
2026-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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NSCLC patients wearing wearable smart devices
NSCLC patients wearing wearable smart devices while utilizing PROs for regular follow-up
Wearable 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.
Interventions
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Wearable 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.
Eligibility Criteria
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Inclusion Criteria
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
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.
18 Years
ALL
No
Sponsors
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The First Affiliated Hospital of Guangzhou Medical University
OTHER
Responsible Party
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Jianxing He
Professor
Principal Investigators
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Jianxing He, M.D
Role: PRINCIPAL_INVESTIGATOR
The First Affiliated Hospital of Guangzhou Medical University
Locations
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Department of Thoracic Surgery and Oncology, The First Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, China
Countries
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Central Contacts
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Facility Contacts
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Wenhua Liang, M.D
Role: backup
Other Identifiers
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WISP-NSCLC
Identifier Type: -
Identifier Source: org_study_id
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