The purpose of this study is to develop and test a smoking cessation intervention for persons who are specifically sensitive to anxiety and anxiety-related bodily sensations.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
University of Vermont
Burlington, Vermont, United States
Smoking status
Time frame: 2 weeks post Quit Day
Smoking status
Time frame: 4 weeks post Quit Day
Smoking status
Time frame: 8 weeks post Quit Day
Smoking status
Time frame: 16 weeks post Quit Day
Smoking status
Time frame: 24 weeks post Quit Day
Where applicable, length of time from Quit Day to relapse.
Time frame: Determined at conclusion of study
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