Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
Healthy Volunteers
ID06628102

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

Age: 50Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

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

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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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