Medical University of South Carolina
Charleston, South Carolina, 29425, United States
NCT Number: NCT03844672
The purpose of this project is to understand how different e-cigarettes influence their likeability and use among current smokers who try using e-cigarettes. Participants will receive an e-cigarette to sample over a three week period. During this time period they will complete daily electronic diaries and weekly lab visits. The results from this information will help understand how different types of e-cigarettes are likely to influence cigarette and e-cigarette use.
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Notify Me21 year and older
All sexes
Interventional
Not applicable
Charleston, South Carolina, 29425, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
include
Exclusion criteria
include
Participants will receive a low power e-cigarette to use for 3 weeks
Participants will receive a high power e-cigarette to use for 3 weeks
Participants will receive a low concentration e-liquid to use for 3 weeks
Participants will receive a high concentration e-liquid to use for 3 weeks
Time frame: Week 3
Participants complete weekly surveys reporting the number of cigarettes smoked each day on a continuous scale
Time frame: Week 3
Participants complete weekly surveys reporting the number of e-cigarette puffing episodes each day on a continuous scale
Time frame: Week 3
Participants complete lab-based choice task at Week 3 visit in which they choose between smoking conventional cigarette and e-cigarette over 10 trials. Outcome is number of times each participant chooses to smoke conventional cigarette.
Medical University of South Carolina
Other
Impact of E-cigarette Characteristics on Reinforcement and Tobacco Use Patterns Among
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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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