The adverse impact of tobacco use on disease prevalence and health care costs is well documented. Hence, finding effective ways to reduce tobacco dependence is an essential component of improving the outcomes, quality and efficiency of VHA care. The U.S. Public Health Service (PHS) Smoking Cessation Clinical Practice Guideline provides specific recommendations for treating tobacco dependence. Despite their strong evidence base, however, these recommendations have not been fully integrated into clinical practice within the VHA. Recent data suggest that logistical difficulties associated with identifying and linking smokers with appropriate treatments may explain why the PHS Smoking Cessation Guideline has not been more broadly implemented. The primary objective of this study is to assess the effectiveness of an intervention for increasing the rate of tobacco dependence treatment in a population of smokers identified through the VA Pharmacy Benefits Management database. Secondary objectives of this study include (1) assessing the effect of the intervention on smoking cessation rates, and (2) developing options for overcoming potential barriers to broad implementation of the strategies. The effectiveness of the intervention will be evaluated using a multi-center, randomized, controlled trial. Veterans receiving a prescription for transdermal nicotine, nicotine gum, or bupropion for smoking cessation in the past year at one of the participating VHA facilities (as determined from Pharmacy Benefits Management records) will be eligible for the study. A total of 1,900 eligible veterans selected from five test sites will be randomly assigned to one of two groups: (1) patient phone call and tailored, computerized prompt to providers (intervention), or (2) usual care (control). The primary outcome is the proportion of patients receiving pharmacological or other smoking cessation treatment in the six month follow-up period, as assessed from VA pharmacy and outpatient data files. All patients will be recruited to a brief phone interview six months post-intervention to gather secondary outcome measure data related to smoking status, quit history, and use of smoking cessation assistance.

Condition	Treatment or Intervention
Smoking Cessation Randomized Controlled Trial	Procedure: Smoking cessation information, collection, and dissemination

Further Study Details: 

Expected Total Enrollment:  1900

Ages Eligible for Study:  19 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

• Subjects must have received a prescription for a smoking cessation medication in 2002.

Minnesota
      VA Medical Center, Minneapolis,  Minnesota,  55417,  United States
      Minneapolis VA Medical Center, Minneapolis,  Minnesota,  55417,  United States
      Minneapolis VA Medical Center, Minneapolis,  Minnesota,  55417,  United States
      VA Medical Center, Minneapolis,  Minnesota,  55417,  United States

Study ID Numbers:  TRX 01-080
Record last reviewed:  March 2005
Last Updated:  March 18, 2005
Record first received:  March 27, 2003
ClinicalTrials.gov Identifier:  NCT00057070
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08