Nicotine Dependence Clinical Trial
Official title:
Lab to Real World Assessment of E-cigarette Abuse Liability and Appeal
The proposed research is a longitudinal human lab study to examine how measures of abuse liability and product appeal vary by e-cigarette device type, and how these lab assessments may predict subsequent e-cigarette and other tobacco use behavior at 1,3, and 6 months. An additional aim is to evaluate e-cigarette safety and tolerability among smokers by device type.
The proposed research is a longitudinal human lab study to involving 6 lab visits and 3
follow-up surveys at 1, 3, and 6 months after participants' last lab visit. Investigators
will enroll 30 smokers (≥10 cig/day) who have not used e-cigarettes in the past 30 days and
have never used e-cigarettes "fairly regularly." After a telephone screening to confirm
eligibility, participants will attend Virginia Commonwealth University's (VCU) Clinical
Behavioral Pharmacology Laboratory for all lab visits. The specific aims are to:
Aim 1. Examine how measures of abuse liability and product appeal vary by ECIG device type
(Markten vs. e-Go).
Aim 2. Compare differences in abuse liability and product appeal between participants' usual
brand of tobacco cigarette, Markten, and e-Go.
Aim 3. As an exploratory aim, examine the extent to which measures of abuse liability and
product appeal as measured in the lab (including TPPT) predict participants' real-world ECIG
use at the 1-, 3-, and 6-month follow-up surveys.
Aim 4. To monitor safety and tolerability the MarkTen and e-Go among smokers.
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