Tobacco use is the leading preventable cause of death in the United States1, and unfortunately, even in empirically supported multi-component tobacco dependence treatment2 trials, most smokers relapse within days of their quit attempt.3 One potentially modifiable relapse risk factor is "task persistence"-the tendency to persist in a difficult task. Because greater task persistence is associated with better smoking cessation treatment outcomes,4-7 an intervention which increases task persistence should result in higher quit rates. Cognitive theory8 indicates that automatic thoughts-such as those which may contribute to low task persistence (e.g., "This stress is unbearable without a cigarette!")-are modifiable. If we can train smokers to modify behaviors and dispute automatic thoughts that contribute to their lack of persistence during a quit attempt, we may be able to improve cessation rates. In this Stage I Behavioral and Integrative Treatment Development (R34) project, we propose to develop a theory-based smoking cessation intervention (called Persistence-targeted smoking cessation;PTSC), including a treatment manual, preliminary training materials, and preliminary therapy integrity scales. After writing a first draft of the PTSC manual, we will use a successive cohort design 9,10 that allows for a structured approach to therapy development. We will recruit two successive cohorts of 5 smokers each to participate in an 8-session, weekly, individual, smoking cessation treatment (PTSC) plus nicotine patch. After treating patients 1-5, we will analyze data and feasibility, and will modify the treatment manual and protocol accordingly before then treating patients 6-10. We will again revise the manual based on data and clinical experience in treating the second cohort before beginning a Stage Ib pilot RCT. In the RCT, we will randomize participants (N=50) to Persistence-Targeted Smoking Cessation + patch (PTSC) or to a manualized version of the National Cancer Institute's "Clearing the Air" + patch (CTA), and assess outcomes at 1- and 3-months after the target quit date. We will test the feasibility and preliminary efficacy of the intervention (i.e., cigarettes per day and prolonged abstinence) and evaluate the relationship between changes in task persistence and smoking cessation success - including testing a mediational model as an experimental hypothesis. Our research team is particularly qualified to successfully conduct the proposed study. We have conducted multiple therapy development studies (including those of CBT) resulting in treatment manuals, developed and used therapy integrity scales, and treated hundreds of smokers in cessation clinics and in NIH clinical trials. This project has strong potential significance because if we can train smokers to dispute automatic thoughts contributing to their lack of persistence during a quit attempt, we may be able to improve cessation rates.

Public Health Relevance

Tobacco use is the leading preventable cause of death in the United States,1 and unfortunately, most smokers relapse within days of their quit attempt.3 Because smokers demonstrating a greater tendency to persist in difficult tasks have better smoking cessation treatment outcomes,4-7 we will design an intervention that increases abstinence-related persistence with the goal of increasing smoking cessation success rates.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Planning Grant (R34)
Project #
5R34DA030652-04
Application #
8513288
Study Section
Special Emphasis Panel (ZRG1-RPIA-K (09))
Program Officer
Grossman, Debra
Project Start
2011-09-30
Project End
2014-07-31
Budget Start
2013-08-15
Budget End
2014-07-31
Support Year
4
Fiscal Year
2013
Total Cost
$159,906
Indirect Cost
$59,336
Name
Rbhs-Robert Wood Johnson Medical School
Department
Psychiatry
Type
Schools of Medicine
DUNS #
078795875
City
Piscataway
State
NJ
Country
United States
Zip Code
08854
Williams, Jill M; Steinberg, Marc L; Griffiths, Kim Gesell et al. (2013) Smokers with behavioral health comorbidity should be designated a tobacco use disparity group. Am J Public Health 103:1549-55