Purpose

This study investigates heavy metal exposure in young adults who use electronic cigarettes.

Condition

Eligibility

Eligible Ages
Between 18 Years and 29 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Aged 18-29 years - Established electronic cigarette (EC) user (participant uses ECs on a daily/weekly basis [used on ≥ 5 days in past 30-days] for the past 3 months) - Willing to abstain from nicotine for at least 12 hours before the laboratory visit - Willing to not eat food or drink water/beverages for at least 30 minutes before the laboratory visit [required for salivary collection] - Utilize 4th generation EC products (pod-mod or disposable EC products; e.g., JUUL, Hyde) - Must be able to read and write in English

Exclusion Criteria

  • Recently COVID-19+ (defined as a positive test in the past 30 days) or a recent COVID-19 hospitalization (within the past 6 months) - Attempting to quit the use of ECs - Is pregnant, planning on becoming pregnant and/or breastfeeding [will be verified using a urine pregnancy test] - Self-reported severe or significant psychological and/or psychiatric conditions [e.g., not currently receiving treatment/medication; only past and/or stable conditions will be allowed] - A history of cardiac events and/or distress within the past 3 months - Diagnosed with a chronic, serious lung disease or current infection (e.g., pneumonia, pulmonary edema) - Are deaf, hard of hearing, or have a severe motor disability

Study Design

Phase
Study Type
Observational
Observational Model
Case-Only
Time Perspective
Cross-Sectional

Arm Groups

ArmDescriptionAssigned Intervention
Observational Participants vape their own electronic cigarette device as much or as little as they like over 30 minutes on study. Participants also undergo saliva sample collection, spirometry to measure respiratory function, and complete questionnaires.
  • Other: Non-Interventional Study
    Non-Interventional Study
    Other names:
    • Non-Interventional Observational Study

Recruiting Locations

Ohio State University Comprehensive Cancer Center
Columbus, Ohio 43210
Contact:
Alayna P. Tackett, PhD
844-744-2447
Tackett-Lab@osumc.edu

More Details

NCT ID
NCT07215065
Status
Recruiting
Sponsor
Ohio State University Comprehensive Cancer Center

Study Contact

The Ohio State University Comprehensive Cancer Center
800-293-5066
OSUCCCClinicaltrials@osumc.edu

Detailed Description

PRIMARY OBJECTIVES: I. Identify and quantify heavy metals (HM) concentration in the saliva of e-cigarette users. II. Examine changes in pulmonary functioning and HM concentration pre/post vaping. III. Examine the association between vaping intensity and HM concentration in the saliva of e-cigarette users. OUTLINE: This is an observational study. Participants vape their own electronic cigarette device as much or as little as they like over 30 minutes on study. Participants also undergo saliva sample collection, spirometry to measure respiratory function, and complete questionnaires.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.