[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100616780":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":26,"locations":26,"responsibleParty":32,"collaborators":26,"id":36,"slug":37,"hasResults":38,"nctId":39,"briefTitle":40,"officialTitle":40,"acronym":26,"eligibilityCriteria":41,"healthyVolunteers":38,"sex":42,"minAge":43,"maxAge":44,"enrollmentInfo":45,"targetDuration":26,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":57,"overallStatus":61,"whyStopped":26,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":26},{"fullName":5,"class":6},"West China Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental","EXPERIMENTAL","Patients in this arm receive standard perioperative care plus a wearable-based digital perioperative rehabilitation program. The intervention includes preoperative personalized exercise training (aerobic exercise, respiratory muscle training, and resistance training), real-time six-minute walk test monitoring, portable pulmonary function testing, and continuous physiological monitoring using wearable devices (heart rate, oxygen saturation, and activity level). After discharge, patients undergo a 30-day home-based digital rehabilitation program with daily exercise tasks, real-time data upload, electronic patient-reported outcomes (ePROs), and remote guidance via a digital platform. Rehabilitation plans are dynamically adjusted based on patient performance and physiological data.",[13],"Device: Wearable-Based Digital Perioperative Rehabilitation System",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Perioperative Care","ACTIVE_COMPARATOR","Patients in this arm receive standard perioperative management only. This includes routine preoperative assessment, standardized surgical and anesthesia care, and conventional postoperative rehabilitation guidance at discharge. No wearable device monitoring, prehabilitation training, or digital home-based rehabilitation platform is provided. Patients are followed according to routine outpatient follow-up schedules after discharge.",[19],"Behavioral: Standard Perioperative Rehabilitation Guidance",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Wearable-Based Digital Perioperative Rehabilitation System","This intervention consists of a wearable-based digital perioperative rehabilitation system designed for patients with non-small cell lung cancer undergoing thoracic surgery. The system integrates continuous physiological monitoring, functional assessment, and remote rehabilitation management. During the preoperative phase, patients receive personalized prehabilitation including aerobic exercise, respiratory muscle training, and resistance training. Wearable devices continuously monitor heart rate, oxygen saturation, activity level, and walking distance, including real-time monitoring during the six-minute walk test. Portable pulmonary function testing and functional MRI (PREFUL) are used for baseline assessment. During the postoperative phase, patients receive 30 days of home-based digital rehabilitation, including daily exercise tasks, real-time data upload, electronic patient-reported outcomes, and remote feedback from clinicians via a digital platform. Rehabilitation plans are dynam",[9],null,{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":26},"BEHAVIORAL","Standard Perioperative Rehabilitation Guidance","This behavioral intervention consists of standard perioperative rehabilitation guidance provided to patients undergoing thoracic surgery for non-small cell lung cancer. Patients receive routine preoperative assessment, standardized postoperative discharge education, and conventional rehabilitation instructions including breathing exercises, early mobilization, pain management, and activity recommendations. No structured prehabilitation program, wearable device monitoring, remote digital platform, or continuous physiological monitoring is provided. Post-discharge follow-up is conducted according to routine outpatient clinical practice.",[15],{"type":33,"investigatorFullName":34,"investigatorTitle":35,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Xuelei Ma MD","Department of Biotherapy, West China Hospital, Sichuan University","100616780","the-construction-and-clinical-application-of-an-integrated-perioperative-management-system-for-lung-cancer-based-on-wearable-devices-and-intelligent-platforms-100616780",false,"NCT07310056","The Construction and Clinical Application of an Integrated Perioperative Management System for Lung Cancer Based on Wearable Devices and Intelligent Platforms","Inclusion Criteria:\n\nAge ≥18 years and ≤85 years\n\nPathologically confirmed primary non-small cell lung cancer (NSCLC)\n\nScheduled to undergo elective curative-intent thoracoscopic lobectomy or segmentectomy\n\nPostoperative clinical condition is stable and judged by investigators to be suitable for discharge within 2-7 days after surgery\n\nAble to independently operate a smartphone and wearable device, or able to do so with caregiver assistance\n\nWilling to comply with study procedures and follow-up requirements\n\nProvided written informed consent prior to participation\n\nExclusion Criteria:\n\nPreoperative long-term home oxygen therapy or severe resting respiratory failure\n\nPresence of severe or uncontrolled cardiopulmonary disease, cerebrovascular disease, hepatic insufficiency, or renal insufficiency\n\nSevere comorbid conditions that significantly limit physical activity or adherence to rehabilitation\n\nKnown or suspected allergy to materials used in wearable devices or medical adhesives\n\nSevere postoperative complications requiring reoperation or prolonged mechanical ventilation\n\nOccurrence of serious adverse events during the six-minute walk test that prevent continuation of the study\n\nAny other condition that, in the judgment of the investigators, makes the participant unsuitable for study participation","ALL","18 Years","85 Years",{"count":46,"type":47},126,"ESTIMATED","INTERVENTIONAL",[50],"NA","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.",[53,54,55,56],"Non-Small Cell Lung Cancer (NSCLC)","Rehabilitation","Thoracic Surgery","Perioperative Management",[58,59,60,56,54],"Non-Small Cell Lung Cancer","Lung Cancer Surgery","Wearable Devices","NOT_YET_RECRUITING","2025-12-29",{"date":64,"type":65},"2025-12-30","ACTUAL",{"date":67,"type":47},"2026-01-01",{"date":69,"type":47},"2026-12-01",{"name":5,"class":6}]