Actively Recruiting
Improving Detection of Early Lung Cancer in a Diverse Population
Led by British Columbia Cancer Agency · Updated on 2024-10-04
3600
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
B
British Columbia Cancer Agency
Lead Sponsor
L
Laval University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to improve early detection of lung cancer in people who are currently at high risk but do not meet existing lung cancer screening criteria. It focuses on individuals with incidental pulmonary nodules (IPNs), which often go without proper follow-up despite their link to lung cancer risk. The study will develop new ways to assess lung cancer risk, including breath and blood tests, and improve interpretation of chest CT scans to better identify and manage these nodules. Participants will provide information about their health, smoking history, and other factors through a questionnaire. They will then give a breath sample using a special device and provide a small amount of blood. Existing chest CT scans will be analyzed with computer software to detect nodules, followed by appropriate monitoring based on current guidelines. The study includes a large group of 3600 people from multiple provinces and plans to validate new tests and technologies to support lung cancer detection. During the study, participants will be asked about their health and history, provide breath and blood samples, and have their CT scans reviewed. Researchers will use these data to develop a risk assessment framework and validate tests over a period of four years. Outcomes include improving lung cancer risk assessment for IPN patients, validating breath and blood tests, enhancing CT scan reading accuracy, and evaluating the cost-effectiveness of these approaches. Participants will be monitored and followed up according to standard clinical guidelines throughout the study.
CONDITIONS
Brief Title
Improving Detection of Early Lung Cancer in a Diverse Population (IDEAL) Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 50 to 80 years
- Able to provide informed consent
- Chest CT scan showing a lung nodule equal to or greater than 6mm
- No other cancers outside of lung cancer for group 1
- Able to abstain from smoking tobacco for 24 hours before breath test
You will not qualify if you...
- Too ill to provide a breath sample
- Smoked tobacco within the last 24 hours
- Pregnant
- Diagnosed with a respiratory infection in the last 3 months
- Unwilling to consent to the study
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)
Duration - Up to 4 years
Participants with incidental pulmonary nodules are monitored to assess lung cancer risk using chest CT scans, breath tests, and blood protein panels.
Periodic visits for assessments and follow-up according to guidelines
Trial Site Locations
Total: 1 location
1
BC Cancer Research, part of the Provincial Health Authority
Vancouver, British Columbia, Canada, V6K 2N2
Actively Recruiting
Research Team
R
Renelle L Myers, MD
C
Crista L Bartolomeu, MSc
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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