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

NCT07310056

RecruitingNA

Sponsor: West China Hospital

Conditions: Non-Small Cell Lung Cancer (NSCLC), Rehabilitation, Thoracic Surgery, Perioperative Management

Interventions: Wearable-Based Digital Perioperative Rehabilitation System, Standard Perioperative Rehabilitation Guidance

Countries: China

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 overview

Sex: ALL

Age: 18 Years to 85 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

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

Locations (1)

Chengdu, China