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Tobacco Use Disorder clinical trials

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NCT ID: NCT00217984 Completed - Clinical trials for Tobacco Use Disorder

Intensive Intervention for Smokers - 6

Start date: July 2006
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the efficacy and cost-effectiveness of an intensive smoking cessation intervention that utilizes extended cognitive-behavioral therapy and combination nicotine replacement (CNR) in a randomized controlled trial. The intensive intervention was compared to usual care involving referral to a free-standing smoking cessation program that provides brief counseling and CNR. We recruited 162 smokers, ages 18 to 75, who are enrolled in the Drug and Alcohol Treatment (DAT) programs at the San Francisco VA Medical Center (SFVAMC) and Santa Rosa VA Community-based Outpatient Clinic (CBOC). To be eligible, participants had to be abstinent from alcohol for at least one week, but not more than 30 days. We compared outcomes for the two study arms by assessing biochemically-validated point-prevalence smoking status at 3, 6, 9, and 12 months post-baseline and continuous abstinence over the 12-month follow-up. Expired-air carbon monoxide (CO) was used to biochemically verify 7-day point prevalence abstinence. We also conducted an economic analysis to determine the cost-effectiveness of the intensive intervention compared with usual care. We also examined cross-relapse patterns during the follow-up period, assessing changes in mood states and use of tobacco, alcohol, and other drugs at 3, 6, 9, and 12 months.

NCT ID: NCT00208858 Completed - Clinical trials for Tobacco Use Disorder

A Pilot Study of the Neural Correlates of Treatment Effect on Nicotine Craving

Start date: December 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to gather pilot data to determine feasibility of and guide the development of a larger clinical trial investigating the effects of topiramate as an adjunct to nicotine replacement therapy and behavioral counseling in smoking cessation treatment. It is hypothesized that topiramate will decrease nicotine craving and result in improved outcomes for smoking cessation.

NCT ID: NCT00184184 Completed - Clinical trials for Tobacco Use Disorder

Registration of Tobacco, Coffee and Substance Use Among Acutely Admitted Psychiatric Patients

Start date: October 2004
Phase: N/A
Study type: Observational

This is a study of the registration of tobacco, coffee and substance abuse among acutely admitted psychiatric patients.

NCT ID: NCT00178685 Completed - Clinical trials for Tobacco Use Disorder

Smokers' Health Project: Self-Determination and Maintaining Tobacco Abstinence

SHP
Start date: August 2004
Phase: Phase 4
Study type: Interventional

These two studies will examine the role of autonomous motivation in maintained adherence. The first study will determine whether smokers are still abstinent from tobacco 32 months after starting in a previous project (Smoker's Health Study). The purpose of the second study is to determine which of three treatments for tobacco dependence provides the greatest amount of protection from relapsing to smoking after quitting. Specifically, the investigators will determine if extending the length of treatment time focusing on relapse prevention and arranging for support from important others prevents relapse compared to community care. Also, the investigators will determine if providing extended treatment time and support from important others plus providing medications to those that don't want to quit prevents long term relapse compared to just extending the length of treatment time and support from others. Additionally, a sub set of the population will be randomized to using hand held palm devices to recover real-time data assessment during the last 10 months of the project.

NCT ID: NCT00176449 Completed - Clinical trials for Tobacco Use Disorder

A Comparison of Bupropion SR and Placebo for Smoking Cessation

Start date: April 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether the adjunctive use of bupropion SR in the context of a psychoeducational program modified for people with schizophrenia might improve the likelihood of successful abstinence in this population. If bupropion SR is effective for reducing cigarette smoking, then it will be important to determine if decreased nicotine intake is associated with a worsening of psychotic, anxiety or depressive symptoms. In addition, it would be important to determine the effect that a reduction in nicotine stimulation would have on patient's cognitive functioning, as nicotinic receptors have been shown to regulate attention and memory function, and it is hypothesized that these functions are normalized by acute nicotine administration in people with schizophrenia

NCT ID: NCT00158171 Completed - Smoking Cessation Clinical Trials

Effectiveness of Various Smoking Cessation Therapies in Reducing Smoking in Adolescents - 1

Start date: April 2002
Phase: Phase 2
Study type: Interventional

Currently one in five high school students smokes. Smoking can harm adolescents well before they reach adulthood by causing a number of immediate, sometimes irreversible, health risks and problems. This study will compare the effectiveness of treatment with bupropion, a nicotine patch, or nicotine gum in supporting the reduction of smoking in adolescent smokers.

NCT ID: NCT00158158 Completed - Smoking Cessation Clinical Trials

Effectiveness of Reducing Smoking in Facilitating Smoking Cessation in Adolescents - 2

Start date: September 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Currently one in five high school students smoke. Smoking can harm adolescents well before they reach adulthood by causing a number of immediate, sometimes irreversible, health risks and problems. This study will examine whether reducing smoking will facilitate quitting smoking in adolescents who have unsuccessfully attempted to quit smoking

NCT ID: NCT00158145 Completed - Clinical trials for Tobacco Use Disorder

Assessing the Variability Over Time of Tobacco Carcinogen Biomarkers in Smokers - 2

Start date: September 2005
Phase: Phase 2
Study type: Observational

Lung cancer is the leading cause of cancer death in the United States. Currently it remains impossible to predict which smokers will get cancer. Each puff of a cigarette delivers a mixture of over 60 known carcinogens. Biomarkers that quantify carcinogen levels and metabolism are a useful tool and available to use. The purpose of this study is to assess the variability of tobacco smoke carcinogen biomarker levels over one year in a group of smokers.

NCT ID: NCT00142831 Completed - Clinical trials for Tobacco Use Disorder

Bupropion as an Adjunct to the Nicotine Patch Plus CBT

Start date: April 1999
Phase: Phase 4
Study type: Interventional

Existing and new pharmacotherapies along with prevention efforts are key to improving smoking cessation rates and reducing the premature morbidity and mortality associated with tobacco use. A number of individuals suffer from both nicotine dependence and depression. The purpose of this study is to determine the effectiveness of bupropion used in combination with the nicotine replacement patch and cognitive behavior therapy (CBT) in treating nicotine dependent individuals also diagnosed with depression.

NCT ID: NCT00136838 Completed - Clinical trials for Tobacco Use Disorder

Effect of Smoking Exposure on Smoking Relapse Following Brief Abstinence - 2

Start date: October 2001
Phase: N/A
Study type: Interventional

Recent research on the effects of nicotine on the brain and behavior presents an opportunity to advance medication development. The purpose of this study is to develop a laboratory model for early-stage testing of new and existing treatments for nicotine addiction. Specifically, the investigators will develop a laboratory model of relapse to cigarette use in nicotine dependent volunteers.