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

Summary

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.

Eligibility

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
* 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
* Any other condition that, in the judgment of the investigators, makes the participant unsuitable for study participation

Conditions6

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