The Construction and Clinical Application of an Integrated Perioperative Management System for Lung Cancer Based on Wearable Devices and Intelligent Platforms

About this trial

Last updated 5 months ago

Study ID

Approval No. 1647 (2024)

Status

Not yet recruiting

Type

Interventional

Phase

N/A

Placebo

Accepting

18 to 85 Years

All Sexes

Trial Timing

Started 5 months ago

What is this trial about?

This study aims to develop and evaluate an integrated perioperative management system based on wearable devices and a digital rehabilitation platform for patients with non-small cell lung cancer (NSCLC) undergoing thoracic surgery. By combining preoperative functional assessment using the six-minute walk test (6MWT), continuous perioperative physiological monitoring, and structured postoperative home-based digital rehabilitation, this randomized controlled trial will investigate whether the wearable-based digital management model improves short-term postoperative pulmonary function, functional recovery, and clinical outcomes compared with standard perioperative care.

What are the participation requirements?

Inclusion Criteria

Age ≥18 years and ≤85 years Pathologically confirmed primary non-small cell lung cancer (NSCLC) Scheduled to undergo elective curative-intent thoracoscopic lobectomy or segmentectomy Postoperative clinical condition is stable and judged by investigators to be suitable for discharge within 2-7 days after surgery Able to independently operate a smartphone and wearable device, or able to do so with caregiver assistance Willing to comply with study procedures and follow-up requirements Provided written informed consent prior to participation

Exclusion Criteria

Preoperative long-term home oxygen therapy or severe resting respiratory failure Presence of severe or uncontrolled cardiopulmonary disease, cerebrovascular disease, hepatic insufficiency, or renal insufficiency Severe comorbid conditions that significantly limit physical activity or adherence to rehabilitation Known or suspected allergy to materials used in wearable devices or medical adhesives Severe postoperative complications requiring reoperation or prolonged mechanical ventilation Occurrence of serious adverse events during the six-minute walk test that prevent continuation of the study Any other condition that, in the judgment of the investigators, makes the participant unsuitable for study participation