Actively Recruiting

Age: 16Years +
All Genders
Healthy Volunteers
ID04616313

Novel Pulmonary Imaging of Lung Structure and Function in Symptomatic and Asymptomatic E-cigarette Smokers

Led by Western University, Canada · Updated on 2025-08-14

150

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

W

Western University, Canada

Lead Sponsor

L

London Health Sciences Centre

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a 5-year study to examine how vaping with e-cigarettes affects lung health over time. The study compares lung function and structure between people who vape e-cigarettes, including those who have never smoked traditional cigarettes and those who have, and a control group of people who have never smoked either. This research uses advanced imaging and testing to better understand the long-term impact of e-cigarette use on lung health. Participants will attend multiple visits over five years, including initial screening and consent, followed by assessments at 12 weeks, 24 weeks, 48 weeks, and annually up to 5 years. Tests include magnetic resonance imaging (MRI) with hyperpolarized xenon-129 gas, computed tomography (CT) scans, pulmonary function tests before and after bronchodilator use, exercise capacity evaluations, blood and sputum analyses, and health questionnaires. Some visits involve in-person testing, while one visit consists of a telephone health update. During the study, participants will have lung health monitored through detailed imaging, lung function tests, exercise testing, and questionnaires. Researchers will assess changes in lung structure, function, respiratory symptoms, and exercise capacity. Data collection focuses on chronic effects by scheduling tests at least four hours after last vaping or smoking. The study aims to identify any abnormalities in lung health related to e-cigarette use compared to non-smokers, with ongoing safety and health monitoring throughout the five-year period.

CONDITIONS

Brief Title

Novel Pulmonary Imaging of Lung Structure and Function in E-cigarette Smokers

Who Can Participate

Age: 16Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Written informed consent must be obtained before any study assessments.
  • Male or female aged 16 years or older.
  • Weekly e-cigarette use for more than 1 year but less than 5 years.
  • Includes 70 participants who never used combustible cigarettes.
  • Includes 70 participants who are former or current combustible cigarette users.
  • Includes 10 healthy participants who never used e-cigarettes or combustible cigarettes as controls.
Not Eligible

You will not qualify if you...

  • Contraindications to MRI such as MRI-sensitive implants, tattoos with MRI-sensitive dye, or severe claustrophobia.
  • Mentally or legally incapacitated individuals unable to provide informed consent or understand written materials.
  • Inability to perform spirometry or plethysmography lung function tests.

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)

Diagnostic Evaluation

Duration - Initial baseline visit and multiple scheduled visits over 5 years

Participants undergo various diagnostic tests including pulmonary function tests, MRI imaging, chest CT scans, cardiopulmonary exercise testing, sputum and blood analysis, and complete respiratory questionnaires to assess lung structure and function.

6 in-person visits and 1 telephone call over 5 years

Long-term Monitoring

Duration - 5 years

Participants are monitored over 5 years to observe changes in lung health, lung function, and respiratory symptoms through repeated diagnostic tests and questionnaires.

Follow-up visits at 12 weeks, 24 weeks (phone call), 48 weeks, and annually at years 3, 4, and 5

Trial Site Locations

Total: 1 location

1

Robarts Research Institute; The University of Western Ontario; London Health Sciences Centre

London, Ontario, Canada, N6A 5B7

Actively Recruiting

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Research Team

G

Grace E Parraga, PhD

A

Angela Wilson, RRT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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