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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04009850
Other study ID # 2000025572
Secondary ID 2U54DA036151-06
Status Terminated
Phase N/A
First received
Last updated
Start date July 1, 2019
Est. completion date January 31, 2022

Study information

Verified date February 2024
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will investigate within-person changes in smoking behavior when current menthol smokers are switched to non-menthol cigarettes and either tobacco or menthol flavored e-cigarettes.


Description:

The goals of this project include evaluating within-subject changes in cigarette satisfaction and smoking behavior after switching from menthol cigarettes and investigating whether outcomes differ between subjects based on use of menthol vs. tobacco flavored e-cigarettes. Within-person changes in cigarette satisfaction and smoking behavior will be assessed during the last week of the non-menthol cigarette smoking period compared to the menthol cigarette smoking period. Preference and use of both the cigarette and e-cigarette products during the switching period will be compared and the extent to which menthol flavored (vs. tobacco) e-cigarettes are preferred among menthol smokers will be evaluated.


Recruitment information / eligibility

Status Terminated
Enrollment 3
Est. completion date January 31, 2022
Est. primary completion date November 9, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 or older - Able to read English - Cigarette smoker Exclusion Criteria: - Seeking smoking cessation treatment - Serious psychiatric or medical condition - Use of other drugs - Unable or unwilling to complete study protocol

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cigarette Brand Switching
Adult smokers will be switched from smoking menthol cigarettes to non-menthol cigarettes
E-cigarette Flavor
Adult smokers will be provided with either menthol or tobacco flavored e-cigarettes in addition to the non-menthol cigarettes

Locations

Country Name City State
United States Yale University New Haven Connecticut

Sponsors (3)

Lead Sponsor Collaborator
Yale University Food and Drug Administration (FDA), National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total Number of Cigarettes Smoked Self-reported total number of cigarettes smoked per day (Timeline Follow Back) Week 6
Secondary E-cigarette Use Self-reported e-cigarette use compared by e-cigarette flavor (Timeline Follow Back) Week 6
Secondary Tobacco Product Satisfaction Self-reported subjective ratings of satisfaction with tobacco products (Modified Cigarette/E-cigarette Evaluation Questionnaire), rated 1-7 with higher scores indicating greater satisfaction Week 6
Secondary Motivation to Quit Smoking Self-reported motivation to quit smoking cigarettes (Contemplation Ladder), rated 1-10, higher scores indicate greater motivation to quit Week 6
Secondary Nicotine Dependence Self-reported nicotine dependence (NIH Promis Dependence Measure), rated 1-5, higher scores indicate greater dependence Week 6
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