The goal of this pilot project is to explore the feasibility of a real-world marketplace study design examining the effects of a reduced nicotine product standard for cigarettes on smoking in the context of a flavor restriction vs. no restriction on e-cigarettes in smokers switched to very low nicotine content cigarettes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
11
Participants with no e-cigarette restrictions.
Participants restricted to tobacco flavored e-cigarettes only.
Masonic Cancer Center
Minneapolis, Minnesota, United States
Percent of participants that drop-out by 4 week visit
Percent of participants that drop-out by 4 week visit
Time frame: 4 weeks
Change in mean cigarettes per day (CPD)
Change in mean cigarettes per day (CPD) based on 7 day ITR data before visit 00 and week 4 visits
Time frame: Baseline to 4 weeks
Number of participants experiencing smoke free days
Time frame: 4 weeks
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