The purpose of the proposed study is to develop an integrated transdiagnostic anxiety disorder treatment and standard smoking cessation treatment for smokers with anxiety disorders (who have been shown to be at high-risk for smoking cessation relapse). The intervention is designed to increase smoking cessation while reducing (1) anxiety symptoms, (2) depressive symptoms, and (3) the cognitive factor of Anxiety Sensitivity, thereby reducing three notable emotional risk factors of smoking cessation relapse and anxiety comorbidity, while at the same time targeting (4) nicotine withdrawal symptoms. The intervention development approach will follow a staged model consistent with NIH guidelines for developing and standardizing behavioral therapies. Accordingly, during the first year, startup activities will include piloting the integrated anxiety-smoking intervention on a subset of individuals, soliciting internal and external expert consultant and participant feedback, and development of the final treatment manual and procedures. The goal during this phase of the project will be to establish feasibility of treatment delivery, participant acceptability, and potetial for an effect. During the following 2 years, a two-arm efficacy study will be undertaken. The two arms of the randomized controlled trial (RCT) will be: (1) standard smoking cessation treatment and nicotine replacement therapy (NRT) plus a transdiagnostic cognitive-behavioral therapy for anxiety (Smoking Termination and Anxiety Reduction Treatment;START) or (2) standard smoking cessation treatment and nicotine replacement therapy plus contact control (ST+CTRL). The primary outcomes of this will be short- and long-term point prevalence abstinence (PPA) and time to first smoking lapse and time to smoking relapse.

Public Health Relevance

Cigarette smoking is the leading cause of death and disability in the United States, contributing to over 440,000 deaths each year, and people with Anxiety Disorders show higher rates of smoking and greater difficulty quitting than people with no psychiatric history or those with other psychiatric conditions. The present project is designed to evaluate a new personalized treatment designed to simultaneously target both smoking and anxiety in this comorbid population.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Planning Grant (R34)
Project #
5R34DA031313-02
Application #
8432033
Study Section
Special Emphasis Panel (ZRG1-RPIA-N (09))
Program Officer
Grossman, Debra
Project Start
2012-03-01
Project End
2015-02-28
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
2
Fiscal Year
2013
Total Cost
$216,360
Indirect Cost
$72,360
Name
University of Houston
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
036837920
City
Houston
State
TX
Country
United States
Zip Code
77204