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N/A N=93 Randomized Double-blind Prevention

Impact of E-cigarette Characteristics on Reinforcement and Tobacco Use Patterns

Smoking · Tobacco Use

Enrolled (actual)
93
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcome: Primary: Mean Cigarettes Per Day — 13.1; 12.6; 12.2; 13.3 cigarettes per day

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Low Power (Behavioral); High Power (Behavioral); Low Concentration (Behavioral); High Concentration (Behavioral)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
Medical University of South Carolina
Primary completion
Oct 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Cigarettes Per Day
13.1; 12.6; 12.2; 13.3
SECONDARY
Average Number of E-cigarette Puffing Episodes
4.8; 6.5; 5.4; 3.0
SECONDARY
Number of Choices to Smoke Cigarette in Lab Setting
1.7; 2.4; 1.8; 2.4

Summary

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.

Eligibility Criteria

Inclusion criteria include

  • adults who have been smoking daily
  • interested in using e-cigarettes
  • who have a smartphone that can receive text messages and access to the internet or has an e-mail account that they check daily

Exclusion criteria include

  • minimal prior e-cigarette use
  • use of tobacco products other than cigarettes
  • current use of cessation medications
  • pregnant, trying to become pregnant, or breastfeeding,
  • recent history of cardiovascular distress in the last three months (e.g., arrhythmia, heart attack, stroke, uncontrolled hypertension),
  • household member currently enrolled in the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03844672). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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