Predicting Symptom Trajectories After Thoracoscopic Lung Cancer Surgery Using an Interpretable Machine Learning Model
1 other identifier
observational
1,500
1 country
1
Brief Summary
Patients suffer from a variety of symptoms after thoracoscopic surgery. However, there is a lack of validated predictive tools to identify potentially high-risk patients. This study is anticipated to include approximately 1,500 lung cancer patients who undergo thoracoscopic surgery. Latent class mixed modeling (LCMM) will be used to dentify subgroups of patients with similar symptom trajectories. Machine learning models were developed to predict postoperative symptom trajectories based on collected information. Effective prediction of postoperative symptoms can help identify high-risk patients and take preventive measures.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 8, 2025
CompletedFirst Posted
Study publicly available on registry
January 13, 2025
CompletedStudy Start
First participant enrolled
March 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2026
CompletedJanuary 13, 2025
April 1, 2024
10 months
January 8, 2025
January 8, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Symptom trajectories after thoracoscopic surgery
Postoperative symptoms of interest included pain, shortness of breath, sleep disturbances, and fatigue.
Within four weeks after thoracoscopic surgery
Eligibility Criteria
Lung cancer patient underwent thoracoscopic surgery and completed the MD Anderson Symptom Inventory-Lung Cancer module postoperatively.
You may qualify if:
- Age 18-80 years old;
- Pathologically diagnosed lung cancer;
- Undergo thoracoscopic surgery, including video-assisted thoracoscopy and robotic-assisted thoracoscopic surgery;
- no prior history of malignancy or lung surgery;
- Have the ability to complete the scale.
You may not qualify if:
- Converted to thoracotomy during thoracoscopic surgery;
- Unable to complete the postoperative scale at least two times;
- Missing data values exceeding 30 percent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Guangdong Provincial People's Hospital
Guangdong, 510080, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Guibin Qiao
Guangdong Provincial People's Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof.
Study Record Dates
First Submitted
January 8, 2025
First Posted
January 13, 2025
Study Start
March 1, 2025
Primary Completion
January 1, 2026
Study Completion
February 1, 2026
Last Updated
January 13, 2025
Record last verified: 2024-04