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OpenTrials
Active, Not Recruiting

NCT Number: NCT05869318

Respiratory Effects of E-Cigarettes in Obese Youth

To determine vaping behaviors and respiratory function in obese and nonobese youth e-cigarette users.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

21 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The Ohio State University

Columbus, Ohio, 43210, United States

About this study

The investigators hypothesize that obese youth e-cigarette users will have increased e-cigarette use that will worsen respiratory function. The approach will involve a clinical trial where vaping behaviors (using puff topography) and respiratory function (spirometry, plethysmography, and diffusion capacity) will be assessed while participants vape with their own e-cigarette and, on a separate visit, with the VUSE e-cigarette.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • a current e-cigarette user (≥1 vaping bout daily) for at least the past 3 months,
  • 21-25 years old,
  • willing to abstain from all tobacco and nicotine for at least 12 hours prior to lab sessions,
  • willing to complete five lab visits lasting up to 4 hours each,
  • able to read and speak English,
  • willing to provide informed consent.

Exclusion criteria

  • self-reported diagnosis of lung disease including asthma or cystic fibrosis
  • history of cardiac event or distress within the past 3 months
  • history of metabolic disease including thyroid disease or diabetes
  • history of orthopedic or neuromuscular problems that preclude exercise
  • currently pregnant (determined using urine pregnancy test), planning to become pregnant, delivered a child in the past 6 weeks even if not breastfeeding, or currently breastfeeding
  • use of other tobacco products >10 days in the past month
  • current marijuana use >10 times per month
  • currently engaging in a vaping cessation attempt
  • ) competitive athlete or individual currently engaged in an exercise training program involving 420min or more (moderate intensity aerobic activity) or 210 min or more (vigorous intensity aerobic activity) per week with the goal of participating in a competitive event or marathon, triathlon, etc. Participants who are engaged in usual physical activity (e.g., walking dog, biking to work, etc.) but not engaged in a "structured exercise training program" will not be excluded.
  • plans to leave the Columbus or central Ohio region within the next year.

Treatment and study plan

ECIG own

Other

Participants will vape using their own ecig device

ECIG Vuse

Other

Participants will vape a VUSE e-cigarette (GOLD 5%)

Primary outcomes

  1. Forced expiratory volume in 1 second

    Time frame: Change from 0 to 35 minutes

    Spirometry will be completed before and after a 35 min vaping session

  2. Functional residual capacity

    Time frame: Change from 0 to 35 minutes

    Plethymosgraphy will be completed before and after a 35 min vaping session

  3. Diffusion capacity

    Time frame: Change from 0 to 35 minutes

    DLCO will be completed before and after a 35 min vaping session

  4. Airway resistance

    Time frame: Change from 0 to 35 minutes

    Plethymosgraphy to measure airway resistance (Raw) will be completed before and after a 35 min vaping session

  5. Puff count

    Time frame: 35 minutes

    E-cig puff topography data collection for abuse liability

  6. Average Puff duration

    Time frame: 35 minutes

    E-cig puff topography data collection for abuse liability

  7. Average Puff volume

    Time frame: 35 minutes

    E-cig puff topography data collection for abuse liability

Secondary outcomes

  1. Tiffany-Drobes Questionnaire of Smoking Urges

    Time frame: Change from 0 to 35 minutes

    Assess E-cig craving/suppression of craving

  2. Respiratory health questionnaire

    Time frame: Change from 0 to 35 minutes

    Assess respiratory symptoms

  3. Exhaled carbon monoxide

    Time frame: Change from 0 to 35 minutes

    Assess carbon monoxide in exhaled air

Sponsors and collaborators

Lead sponsor

Ohio State University Comprehensive Cancer Center

Other

Registry information

Official study title

RESEC: Respiratory Effects of E-Cigarettes in Obese Youth

Acronym: RESEC

Important dates

Study start
2023
Primary completion
2024
Study completion
2027
First posted
May 22, 2023
Registry last updated
Oct 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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