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Effects of e-Cigarettes on Perceptions and Behavior

Effects of e-Cigarettes on Perceptions and Behavior

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03742817
Enrollment
45
Registered
2018-11-15
Start date
2019-02-01
Completion date
2020-03-01
Last updated
2023-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Electronic Cigarettes

Brief summary

This project will assess the ways in which e-cigarette product diversity impacts the user experience to inform potential regulations by identifying product characteristics that may: (1) put young adults at risk for tobacco product use; and (2) facilitate adult smokers switching to e-cigarettes. There are three primary objectives to the study: (1) Determine which dimensions of e-cigarette product diversity differentially affect product appeal across young adult e-cigarette users and middle-age/older adult smokers with an interest in, but no significant experience with, e-cigarettes; (2) Determine which dimensions of e-cigarette product diversity differentially affect abuse liability in young adult e-cigarette users and the ability to resist smoking in adult smokers with an interest in, but no significant experience with, e-cigarettes; (3) Determine the affect of product characteristics on e-cigarette nicotine delivery profile. For Aim 1, young adult vapers (N=200) and adult smokers (N=200) will attend one laboratory session in which they will self-administer e-cigarette products varied according to within-subject e-cigarette factors (e.g., flavor, pg/vg ratio). For Aim 2, young adults vapers (N=360) and adult smokers (N=360) will administer an e-cigarette product and complete behavioral economic tasks that test the participant's choice of earning money to delay initiation and continued use of: (1) The sampled e-cigarette product (abuse liability; young adult vapers); or (2) Their own brand cigarettes (ability to resist smoking; adult current smokers). A pilot study will establish device and e-liquid parameters (e.g., nicotine concentration) to be used for all aims.

Interventions

OTHERe-Cigarette

Participants will self-administer an experimenter-provided e-cigarette.

Sponsors

University of Southern California
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Vapers 1. E-cigarette use \>3 day/week for \>2 months 2. Report regularly using e-cigarette products with nicotine 3. Positive cotinine test via NicAlert test strip Smokers 1. Daily cigarette smoking for ≥ 2 years 2. Currently smoke \> 4 cig/day 3. Interest in trying an e-cigarette or current use of e-cigarettes

Exclusion criteria

Vapers 1. Pregnancy/breastfeeding 2. Desire to immediately reduce e-cigarette use Smokers 1. Breath CO \< 9ppm at intake 2. Pregnancy / breastfeeding 3. Current daily use of other combustible tobacco products (e.g., cigars)

Design outcomes

Primary

MeasureTime frameDescription
Subjective Appeal1 hourSelf-report measures of product appeal will be completed following the e-cigarette administration.
Positive Affect Negative Affect Schedule4 hoursThe 10-item Positive Affect Negative Affect Schedule (PANAS-SF) will be used to measure positive and negative affect.
Questionnaire of Vaping Urges4 hours10-item Brief Questionnaire of Vaping Urges will assess desire, intention, urge and need to vape e-cigarettes.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026