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Tobacco Use Disorder clinical trials

View clinical trials related to Tobacco Use Disorder.

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NCT ID: NCT02839382 Completed - Clinical trials for Cardiovascular Disease

The Northwest Coalition for Primary Care Practice Support

H2N
Start date: May 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this project is to build capacity for quality improvement (QI) in small primary care practices across Washington, Oregon and Idaho by improving risk factors for heart attacks such as blood pressure, cholesterol and smoking. The Northwest Coalition for Primary Care Practice Support will assist practices by providing them with a QI coach, creating group learning opportunities, and conducting educational outreach activities. An innovative study design will be used to determine what levels and types of support are most helpful and effective.

NCT ID: NCT02781090 Completed - HIV Clinical Trials

RCT of an Internet Cessation Program Plus Online Social Network for HIV+ Smokers

PSFW+
Start date: July 6, 2016
Phase: N/A
Study type: Interventional

This trial will compare the efficacy of Positively Smoke Free on the Web+ (a smoking cessation program + social network for HIV-infected smokers) to the American Heart Association Getting Healthy website in promoting abstinence in a group of HIV-infected smokers. All participants will be offered a three-month supply of nicotine patches.

NCT ID: NCT02781038 Completed - Clinical trials for Tobacco Use Disorder

Smoking Cessation and a Teachable Moment in Patients With Acute Fractures

Start date: February 2014
Phase: N/A
Study type: Interventional

Patients who smoke and suffer from fractures are worse off than those who do not smoke. Orthopaedic patients represent a group that can benefit from physician contributions to smoking cessation, and a special opportunity to cue this can begin with the orthopaedic surgeon in the acute setting. However, the best way to appropriately counsel these patients and assess the impact as a teachable moment remains undetermined.

NCT ID: NCT02773836 Completed - Tobacco Dependence Clinical Trials

European Regulatory Science on Tobacco: Policy Implementation to Reduce Lung Diseases (EUREST-PLUS)

EUREST-PLUS
Start date: June 15, 2016
Phase:
Study type: Observational

The main objective of EUREST-PLUS is to monitor and evaluate the impact of the Tobacco Products Directive (TPD) within the context of FCTC ratification at an EU level. The investigators specific objectives, within WorkPackage 2 and Workpackage 3 are: To evaluate the psychosocial and behavioral impact of TPD implementation and FCTC implementation, through the creation of a cohort study of adult smokers in 6 European Member States (EU MS), Germany, Greece, Hungary, Poland, Romania, Spain; (total n=6000) in a pre- vs. post-TPD study design. EUREST-PLUS is funded through the European Union's Horizon 2020 research and innovation programme under grant agreement No 681109

NCT ID: NCT02764385 Completed - Smoking Clinical Trials

Using a Teachable Moment Communication Process to Improve Outcomes of Quitline Referrals

Start date: August 2016
Phase: N/A
Study type: Interventional

This study will compare the effectiveness of two approaches for delivering smoking cessation advice in the primary care setting. Ask-Advise-Connect (AAC) is a strategy that uses the electronic health record (EHR) to prompt clinical staff to Ask if the patient smokes, Advise them to quit and, if they're interested, Connect them to Quitline (QL) counseling services. The connection occurs when a QL counselor is notified of the patient's interest, and then calls the patient to enroll in treatment. AAC has been shown to be very effective at enrolling patients, however, it was found that less than 42% of patients who agreed to be referred were successfully contacted by the QL after 5 call attempts. This indicates that many patients that are referred are not ready for cessation, but may feel obligated to accept the referral from their primary care team. This presents an opportunity to improve the patient centeredness of the referral process. To overcome these limitations, the investigators propose pairing it with a patient-centered smoking cessation approach called the Teachable Moments Communication Process (TMCP). The investigators' team developed this communication strategy, which incorporates patients' concerns into a partnership-oriented discussion about smoking cessation. The investigators propose that combining these two approaches could increase appropriate referrals to the QL, increase the likelihood of successful patient contact and enrollment, and increase the patient's rating of the value of the experience.

NCT ID: NCT02740595 Completed - Nicotine Dependence Clinical Trials

E-cigarettes and Blood Vessel Function

Start date: August 2015
Phase: N/A
Study type: Interventional

Randomized controlled trial of electronic cigarettes with nicotine, without nicotine, and sham control, on endothelial function and markers of oxidative stress.

NCT ID: NCT02737358 Completed - Smoking Clinical Trials

N-acetylcysteine for Tobacco Use Disorder

Start date: August 30, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the effects of administering N-Acetylcysteine (NAC) to assist in initial cessation and/or relapse prevention in adult cigarette smokers.

NCT ID: NCT02724241 Completed - Nicotine Dependence Clinical Trials

E-Cigarettes and SNA

Start date: April 2015
Phase: N/A
Study type: Interventional

Randomized controlled trial of electronic cigarettes with nicotine, without nicotine, and sham control, on sympathetic nerve activity and markers of oxidative stress.

NCT ID: NCT02723162 Completed - Clinical trials for Nicotine Dependence, Cigarettes

Translational Neuropsychopharmacology Research of Nicotine Addiction

Start date: May 4, 2016
Phase: Phase 2
Study type: Interventional

This study will examine the effects of combining Varenicline (VRN) and N-acetylcysteine (NAC) on neural circuitry function and treating nicotine addiction. Healthy adult nicotine dependent cigarette smokers interested in quitting (n=110) will be randomized to one of four PBO-controlled conditions for 4 weeks: 1) VRN+NAC, 2) VRN+PBO, 3) NAC+PBO or 4) PBO+PBO. Following 1 week of medication, participants will be contingently reinforced for 3 days of smoking abstinence and be scanned using functional magnetic resonance imaging (fMRI) techniques, while nicotine deprived during a resting state and a cue-reactivity (CR) task. Participants will be followed over the next 3 weeks of treatment and clinical variables will be assessed.

NCT ID: NCT02713594 Completed - Smoking Cessation Clinical Trials

Wisconsin Tobacco Quit Line Medicaid Incentive Evaluation

Start date: April 2013
Phase: N/A
Study type: Interventional

The study is designed to test the hypotheses that financial incentives can increase both participation in smoking cessation treatment and resulting cessation rates, when they are offered to BadgerCare Plus (Medicaid) smokers as part of their health care.