N/A
N=93
Impact of E-cigarette Characteristics on Reinforcement and Tobacco Use Patterns
Smoking · Tobacco Use
Bottom Line
View on ClinicalTrials.gov: NCT03844672 ↗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
| Outcome | Result | p-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.
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.