Actively Recruiting
Construction and Evaluation of a Hospital-Community Health Collaboration Model Empowered by Digital Technology for Lung Cancer Screening
Led by The First Affiliated Hospital of Guangzhou Medical University · Updated on 2025-05-30
16000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a digital empowerment model for lung cancer screening aimed at detecting lung cancer earlier and reducing deaths from respiratory diseases. This single-arm cluster randomized trial is conducted in Guangzhou, focusing on community health service centers. The study assesses the effectiveness and cost-effectiveness of low-dose CT (LDCT) screening combined with AI technology and digital health platforms to improve early lung cancer diagnosis. The intervention includes low-dose CT screenings performed at primary healthcare institutions, supported by an AI-based full-lung model that assists in interpreting CT images. Community health centers use a digital platform called "Fei Anxin" to manage resident information and coordinate screening efforts. Participants with detected lung nodules are referred to hospitals for further examination. The study expects to enroll about 16,000 participants and collects individual data through questionnaires and digital tools. Participants will undergo lung cancer screening and complete health questionnaires. Screening and diagnostic data are gathered via digital platforms and hospitals. Researchers will measure the proportion of early-stage lung cancer detected within one year after intervention implementation, along with secondary outcomes like follow-up rates, diagnosis rates, false positive rates, and complications related to CT screening and diagnostic tests. The study runs from June 2024 through June 2025 and involves ongoing monitoring and data collection throughout this period.
CONDITIONS
Brief Title
Early Intervention Strategies for Lung Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Community health service center must be located in one of the 11 districts of Guangzhou
- The center manages over 10,000 elderly residents
- The center has at least one CT machine and qualified medical staff
- Individuals aged 40 to 75 years
- Residing long-term in participating community
- No known history of lung cancer
- No lung cancer screening in past three months
- Able to understand and willing to sign informed consent
- Able to participate in long-term follow-up
You will not qualify if you...
- Community health centers involved in other public health projects affecting screening
- Centers where data collection or follow-up is not possible
- Individuals diagnosed with lung cancer
- Individuals with severe health issues unsuitable for CT imaging
- Individuals unable to understand the study or provide informed consent
- Participants in other clinical trials affecting study results
- Individuals unable to undergo follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) for eligibility assessment and consent
Duration - Up to 1 year
Participants undergo low-dose CT lung cancer screening supported by digital health technology and AI-assisted image interpretation.
Screening performed once at primary healthcare institutions with digital follow-up through the health platform
Duration - Up to 1 year after screening
Participants with detected lung nodules are referred for further diagnostic examinations and followed for up to one year to monitor outcomes including diagnosis and complications.
Follow-up visits depending on diagnostic results, including a 3-month and 1-year follow-up
Trial Site Locations
Total: 1 location
1
Department of Cardiothoracic Surgery, the First Affiliated Hospital of Guangzhou Medical College
Guangzhou, Guangdong, China, 510120
Actively Recruiting
Research Team
J
Jianxing He, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SCREENING
Number of Arms
1
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