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Smoking Behaviors clinical trials

View clinical trials related to Smoking Behaviors.

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NCT ID: NCT05108649 Recruiting - Cigarette Smoking Clinical Trials

Impact of Nicotine Messaging on Beliefs and Behavior

Start date: March 2, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effect of nicotine messaging and nicotine content of study cigarettes on nicotine beliefs and subsequent use of tobacco and nicotine products.

NCT ID: NCT05049174 Active, not recruiting - Clinical trials for Cardiovascular Diseases

Nurse-led Smoking Cessation Program With Follow-up in Healthy Life Centres: a Randomized Clinical Trial

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

A better understanding of how to incorporate effective smoking cessation measures into clinical practice is requested. In this is prospective, multi-center, randomized, open, blinded end-point (PROBE) trial, we assigned daily smokers hospitalized with an acute cardiac event 1:1 to an in-hospital nurse-led smoking cessation intervention with direct referral to further follow-up in the municipal healthy life-centres (intensive intervention) or to written information about smoking cessation and the municipal program (low-threshold intervention) . The primary outcome will be the smoking cessation rates between the groups at 6 months follow-up. Key secondary outcomes include a cost-effectiveness analysis of the intensive intervention and cessation rates at 3- and 12-months follow-up, the proportion who used nicotine replacement therapy and the proportion who attended the healthy-life center program between the two groups. We also assess effects of recurrent cardiovascular events and mortality after 12 months, two and five years follow-up. Exploratory analyses include new knowledge about the patient and system factors of importance for participation to healthy life-centers and for changes in smoking behaviour.

NCT ID: NCT05016505 Recruiting - Smoking Cessation Clinical Trials

Supporting Smoke-Free Policy Compliance in Public Housing

Start date: February 3, 2022
Phase: N/A
Study type: Interventional

This project seeks to determine the effectiveness of two types of interventions to reduce exposure to secondhand smoke in residential buildings. One intervention is geared toward all building residents (resident endorsement) and the other targets smokers (smoking reduction via relocation and reduction in personal smoking/cessation) with the goal of reducing personal smoking and secondhand smoke exposure.

NCT ID: NCT05000632 Recruiting - Smoking Behaviors Clinical Trials

Smoke Free SafeCare: Establishing a Smoke Free Home in CPS-involved Families

SFSC
Start date: April 19, 2022
Phase: N/A
Study type: Interventional

Smoke Free SafeCare (SFSC) is a proposed braided intervention consisting of two evidence-based interventions: Some Things are Better Outside (STBO), aimed at promoting smoke free home rules, and SafeCare, aimed at reducing child maltreatment and improving mother and child outcomes. STBO is effective in creating smoke free homes and reducing second-hand smoke in low-SES (socioeconomic status) households. SafeCare is an effective parent training program that is broadly disseminated in child protective services in the United States. SafeCare is a promising mechanism to effectively increase the reach of STBO to reduce SHS (secondhand smoke) exposure in families with documented high rates of tobacco use and children with cumulative risk for negative health outcomes.

NCT ID: NCT04891939 Not yet recruiting - Smoking Cessation Clinical Trials

Development and Assessment of a Teacher-led Intervention in Preventing Tobacco Use Among the Youth in Ghana

Start date: June 2021
Phase: N/A
Study type: Interventional

The main purpose of this experimental study is to compare the existing health education program for School Health and Education Program (SHEP) in the Junior High Schools with a new health education model (Smart-Kids') for the prevention of smoking initiation and to improve the quit rate among students in Upper East Region of Ghana. The intervention will be based on the Theory of Triadic Influences (TTI) which involves the cultural environment in which adolescents mature, their immediate social situation, and intrapersonal differences. These three factors impact through different mediating variables, such as attitudes, normative beliefs, and self-efficacy, which eventually affect smoking intentions and smoking behavior as the outcome measures. The study design is a cluster randomized control trial. After baseline assessment, the investigators will randomize schools to receive the new health education for three months whiles the comparator (control group) will continue with the usual health education. The investigators will conduct a post-intervention assessment using the same questionnaire with unique identity codes linking each participant to their baseline assessments immediately at the end of the intervention. Final assessment will be done approximately three months after the intervention. The investigators will assess and compare the effectiveness of the new health model to the normal health promotion programs (SHEP). The investigators hypothesized that there will be no significant differences observed between the new teacher-led health education program (the Smart-Kids Program) and the existing SHEP coordinator-led in preventing smoking uptake among the youth. Alternatively, the new teacher-led health education program would facilitate the effects of the program on outcomes. on four key primary endpoints as follows: - H1: The intervention study will result in a 30% reduction in smoking uptake - H2: The intervention study will result in a 10% reduction in smokers - H3. The intervention will increase knowledge of the harmful effects of tobacco use by 50% - H4. The intervention will increase the willingness to quit smoking by 10% among smokers

NCT ID: NCT04861428 Terminated - Smoking Behaviors Clinical Trials

Heat-not-burn Tobacco Product to Aid in Switching From Combustible to Noncombustible Nicotine (IQOS)

IQOS
Start date: June 23, 2021
Phase: N/A
Study type: Interventional

A novel heat-not-burn tobacco product (IQOS) will be provided to smokers, compared against a (cigarette) smoking as usual period in counter-balanced order in a cross-over design. This study will examine the short-term effects of IQOS, switching from combustible to noncombustible nicotine and withdrawal-related symptoms over a two week-long "practice" period, relative to smoking as usual.

NCT ID: NCT04857515 Completed - Smoking Cessation Clinical Trials

Clinical Learning Study for a Mobile Smoking Cessation Program

Start date: March 12, 2021
Phase:
Study type: Observational

The purpose of this study are to obtain learnings regarding the Digital Therapeutic (DTx) experience of Clickotine, including acceptability and preference of the overall program and specific DTx components, as well as to obtain learnings related to adult participants' use of the DTx for smoking cessation.

NCT ID: NCT04808609 Completed - Hiv Clinical Trials

Smoking Cessation Pilot for People Living With HIV (PLWH)

Start date: October 6, 2020
Phase: N/A
Study type: Interventional

The overall goal of this pilot study is to evaluate the feasibility of the Lumme smartphone app for smoking cessation in people living with HIV (PLWH) and evaluate its effect on smoking cessation. Mobile health (mHealth) technology can be used for achieving health equity in vulnerable groups because it is a widely available and relatively inexpensive tool for health behavior change and can be adapted to meet the needs of its end-users. Therefore, a mHealth intervention such as the Lumme App proposed through this study is timely, relevant, scalable and likely to improve health outcomes in PLWH who smoke.

NCT ID: NCT04772144 Completed - Clinical trials for Cardiovascular Diseases

Nurse-led Smoking Cessation With Further Follow-up in Lifestyle Centres - a Randomized Pilot Study

Start date: February 25, 2021
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled pilot study is to test whether an in-hospital nurse-led smoking cessation intervention increases the refferal rate to healty life-centers in the municipalities. We will also describe the proportion who succeed in quitting smoking between the intervention group and the control group and obtain new knowledge about the patient and system factors of importance for participation to healty life-centers and for successful and unsuccessful smoking cessation.

NCT ID: NCT04751461 Completed - Smoking Clinical Trials

CSD210202: A Study to Assess Nicotine Uptake From Electronic Nicotine Delivery Systems

Start date: February 23, 2021
Phase: N/A
Study type: Interventional

This is an open-label, randomized, 5-way crossover study designed to evaluate plasma nicotine pharmacokinetic (PK) parameters following an ad libitum use of Electronic Nicotine Delivery System (ENDS) investigational products (IPs) in a confinement setting by generally healthy combustible cigarette (CC) smokers.