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The Impact of E-liquid Nicotine Content on Reinforcement in Current Smokers

The Impact of E-liquid Nicotine Content on Reinforcement in Current Smokers

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03186911
Enrollment
0
Registered
2017-06-14
Start date
2019-07-31
Completion date
2019-09-30
Last updated
2019-08-05

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

Conditions

Tobacco Use

Brief summary

Participants will complete a phone screen and then one laboratory session. After completing in-person screening assessments, eligible participants will complete additional questionnaires. Participants will then choose an e-liquid flavor to use for the rest of the session. Participants will then sample two e-liquids that vary in nicotine content from little or no nicotine to a moderate level of nicotine, and questionnaires evaluating the subjective effects of each one. Participants will then complete a preference assessment where they choose between the two e-liquids. Participants will be blind to the nicotine contents.

Interventions

BEHAVIORALE-liquid sampling and preference assessment

Participants will sample two different e-liquids that vary in nicotine content, complete questionnaires about each one, and then choose between the two e-liquids in a preference assessment task.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

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

Inclusion criteria

* At least 18 years old * Daily cigarette smoking * Have tried vaping devices on a minimum of one lifetime occasion

Exclusion criteria

* Unwilling to use a vaping device during the session * Break alcohol level \> 0.01 (g/dL) * Pregnant, trying to become pregnant, or breastfeeding * Systolic BP greater than or equal to 160 mm/Hg or below 90 mm/Hg * Diastolic BP greater than or equal to 100 mm/Hg or below 50 mm/Hg * Heart rate greater than or equal to 105 bpm or lower than 45 bpm * A current upper respiratory infection, recent cardiac event (in the last year), Buerger disease, irregular heartbeat or arrhythmia within the last year, previous allergic or adverse reaction to nicotine

Design outcomes

Primary

MeasureTime frameDescription
Product Evaluation QuestionnaireOne DayRatings of the two e-liquids on a self-report questionnaire

Secondary

MeasureTime frameDescription
Preference AssessmentOne DayChoices of each of the two e-liquids on a preference assessment
Perceived Health Risk QuestionnaireOne DayPersonal Health Risk Ratings about each of the two e-liquids
Vaping Purchase TaskOne DayHypothetical estimates of consumption of each of the e-liquids across a variety of prices

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026