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Development of an Artificial Intelligence-Based Comprehensive Management System for Lung Cancer Patients During Operable Period: Part III - Subsystem for Individualized Continuation of Outpatient Rehabilitation

Development of an Artificial Intelligence-Based Comprehensive Management System for Lung Cancer Patients During Operable Period: Part III - Subsystem for Individualized Continuation of Outpatient Rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106590
Enrollment
Unknown
Registered
2025-07-25
Start date
2025-07-31
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung cancer

Interventions

Experimental group: Self-control (Part I):Therefore, it is necessary to carry out a consistency test between the wearable device (Xiaomi bracelet) and the medical monitor, dynamically collect the pati
Intervention group (Part II):1. Daily Exercise Prescription: Time: Developed by the rehabilitation therapist before 17:00 each day based on the data collected on that day. Aerobic Training: Controlled
Control group (Part II):Usual care

Sponsors

Peking University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Part I: Age 18-75 years Patients 24-72 hours after radical resection of thoracoscopic lung cancer Clear awareness and able to cooperate with monitoring Voluntarily sign the informed consent form Part 2: Age 18-75 years Patients 24-72 hours after radical resection of thoracoscopic lung cancer Clear awareness and able to cooperate with monitoring Voluntarily sign the informed consent form

Exclusion criteria

Exclusion criteria: Part I: Combined with severe arrhythmias Skin allergies Limb mobility disorders affect device wear Combined with other vital organ failure Part 2: Combined with severe arrhythmias Skin allergies Limb mobility disorders affect device wear Combined with other vital organ failure

Design outcomes

Primary

MeasureTime frame
Pulmonary Function Recovery Rate (FEV1% Predicted Value);Consistency of Xiaomi Mi Band and Medical Monitor in Heart Rate Monitoring Data (Part 1);Lung function recovery rate (Part II);

Secondary

MeasureTime frame
Differences in consistency between heart rate and SpO2 monitoring data at different time points (6 a.m., 12 a.m. during the day, and 20 a.m.) (Part I);Patient adherence to the Xiaomi Mi Band (Part I);Quality of life score (Part II);Rate of change in 6-minute walking distance (Part II);Complication rate (Part II);

Countries

China

Contacts

Public ContactNan Wu

Peking University Cancer Hospital

nanwu@bjmu.edu.cn+86 10 8819 6530

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026