NCT07588737Recruiting
Multimodal AI-Guided Recovery Management After Lung Cancer Surgery
Multimodal Artificial Intelligence-Guided Symptom Monitoring and Recovery Management After Lung Cancer Surgery: A 20-Center Prospective Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 15 May 2026
Brief summary (registry, in English)
This study is a multicenter, prospective, randomized controlled trial designed to evaluate the effectiveness and safety of a multimodal artificial intelligence (AI)-guided postoperative recovery management system in patients after lung cancer surgery. Eligible patients will be enrolled after surgery when their clinical condition is stable and will be randomly assigned to either an AI-guided recovery management group or a usual postoperative care group. Patients in the AI-guided group will receive usual postoperative care plus a multimodal AI-based recovery management system. The system will collect patient-reported symptoms, vital signs, physical activity, respiratory rehabilitation information, recovery-related data, and, when needed, wound or chest-related images or short videos. Based on these data, the system will provide recovery feedback, general nursing advice, respiratory rehabilitation reminders, activity guidance, and risk stratification alerts. For red-flag symptoms or high-risk conditions, the system will advise patients to contact the clinical team or seek medical care. Patients in the usual-care group will receive standard postoperative management after lung cancer surgery and will complete symptom assessments at the same prespecified time points, but they will not receive AI-generated individualized recovery feedback or AI-generated risk alerts. The primary outcome is the number of MDASI-LC-derived target symptom threshold events within 30 days after surgery. Target symptoms include pain, fatigue, disturbed sleep, shortness of breath, and cough. Secondary outcomes include overall target symptom burden, quality of recovery, time to recovery to a mild-symptom state, functional interference, respiratory rehabilitation adherence, physical activity adherence, unplanned healthcare utilization, pulmonary complications, and unplanned readmission.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 868 (estimated)
- First submitted
- 9 May 2026
- Start date
- 1 Mar 2025
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- The First Affiliated Hospital of Guangzhou Medical University
- Diseases
- Lung cancer
- NCT number
- NCT07588737
What you commit to
- Study type: Interventional
- Planned participants: 868
- From 1 Mar 2025 to the primary completion date, 31 Dec 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients receiving non-surgical treatment only.
- Patients undergoing bronchoscopy, percutaneous biopsy, or other non-surgical diagnostic or therapeutic procedures only.
- Clinically unstable after surgery and unable to participate in symptom assessment or recovery management.
Other illness
- Severe cognitive impairment, psychiatric disorder, language communication disorder, or other conditions that preclude completion of study assessments.
- Any other condition judged by the investigator to make the patient unsuitable for participation in this study.
Other
- Requiring prolonged intensive care unit treatment, continuous advanced life support, or continuous intensive medical management.
- Unable to use a smartphone or study device and without a caregiver who can assist with use.
- Currently participating in another interventional clinical study that may affect the primary outcome of this trial.
Who the study is looking for
- Age 18 years or older.
- Clinically or pathologically diagnosed with lung cancer.
- Undergoing lung cancer-related thoracic surgery.
- Surgical procedures may include video-assisted thoracoscopic surgery, robot-assisted thoracic surgery, or open thoracic surgery.
- Surgical extent may include wedge resection, segmentectomy, lobectomy, sleeve resection, combined resection, bilobectomy, or pneumonectomy.
- Clinically stable after surgery and able to participate in symptom assessment and postoperative recovery management.
- Able to use a smartphone or study device, or has a caregiver who can assist with use.
- Able to complete patient-reported symptom assessments and postoperative recovery information reporting.
- Provides written informed consent.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| the First Affiliated Hospital of Guangzhou Medical University, Guangzhou,Guangdong 510120 Coordinator of this site? Confirm its status | Guangzhou | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.