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Nicotine and Cannabis Vape Labeling Experiment - Spring 2025

Longitudinal Patterns of Non-Combustible Tobacco Product Use in Adolescents (EPIC) / Assessing Development Patterns of Vaping, Alcohol, Nicotine, and Cannabis Use and Emotional Well-being (ADVANCE)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06919276
Acronym
EPIC/ADVANCE
Enrollment
3048
Registered
2025-04-09
Start date
2025-03-03
Completion date
2025-06-01
Last updated
2026-05-22

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

Conditions

Adolescent, Cannabis, Electronic Cigarette Use, Nicotine, Vaping

Keywords

vaping device, product labeling, use susceptibility, perceived harm, nicotine, cannabis

Brief summary

This study assesses how the ways in which nicotine and cannabis vaping devices are labeled impact use susceptibility, anticipated effects, and health harm.

Detailed description

The primary objectives of the study: (1) Determine whether different device labels with the contained substance (nicotine or cannabis) affect adolescent use susceptibility, anticipated effects or impairment, and perceived health harms; (2) Determine whether device color/product flavor differentially impact the study outcomes.

Interventions

OTHERVaping Device Labeling

Participants will view one vape image (experimental stimulus) and are randomized to a label presented and the color/flavor of the vaping device presented. The label conditions are: 1. plain (i.e., no labeling on device) 2. "contains THC" 3. "contains 80% THC" 4. "contains 80% THC - HIGH POTENCY" 5. "contains nicotine" 6. "contains 5% nicotine" 7. "contains 5% nicotine - HIGH STRENGTH" The color/flavor conditions are: mint/mint, white/original, blue/blueberry.

Sponsors

University of Southern California
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH

Study design

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

Intervention model description

Participants will be randomized to one of seven labeling conditions and one of three device colors/flavors.

Eligibility

Sex/Gender
ALL
Age
11 Years to 19 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants must be enrolled in a partnering high school.

Exclusion criteria

* Participants who cannot independently understand study consent and the study surveys are ineligible.

Design outcomes

Primary

MeasureTime frameDescription
Use Intention Susceptibility5 minutesThis 3-item self-report measure assesses participant interest in trying the vaping device in the future. A 4-level Likert scale is used: definitely not, probably not, probably yes, definitely yes.
Perceived Health Harms5 minutesThis 2-item self-report measure assesses participant perception of health harms and risks associated with using the vaping product. A 4-level Likert scale is used: definitely not, probably not, probably yes, definitely yes.
Anticipated Subjective Effects5 minutesThis 9-item self-report measure assesses anticipated subjective effects from using the vaping device. Participants will select all that apply.
Anticipated Impairment/Enhancement5 minutesThis 4-item self-report measure assesses participant anticipated enhancement or impairment effects on completing different activities due to using the vaping product. A 5-level Likert scale is used: definitely make it harder, probably make it harder, no effect, probably make it easier, definitely make it easier.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026