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临床试验/NCT04819152
NCT04819152Unknown不适用

Effectiveness of Tobacco Cessation Interventions for Different Groups of Users in Sweden: a National Prospective Cohort Study

Lund University8 个研究点 分布在 1 个国家目标入组 8,000 人开始时间: 2020年4月9日最近更新:
适应症

试验速览

阶段
不适用
入组人数
8,000
试验地点
8
主要终点
% of patients that are continuously smokefree

研究概览

简要总结

Smoking is still one of the most important risk factors causing morbidity and mortality in Sweden. Every year, 12,000 Swedish citizens die prematurely from smoking, and smoking is responsible for up to 60% of the inequity in health.

Though the smoking prevalence is relatively low in Sweden in an international context (8% and 10% for men and women respectively in 2016), specific vulnarable groups have a very high prevalence; e.g. about 80% in alcohol and drug abusers. Furthermore, Sweden has a unique high prevalence of snus users and in 2016 the daily use of tobacco was 25% for men and 14% for women. In addition, products such as cigarettes, snus, and e-cigettes are often mixed.

Despite the fact that about a thousand counsellors have been trained in manual-based person-centred tobacco cessation interventions in Sweden, the effectiveness of the interventions remains unknown, as a follow-up on effect of in-person interventions is not systematically collected in Sweden. Therefore, as of today it is not possible, on a national level, to compare the effectiveness of differences in these interventions, providers, or different groups of tobacco users including disadvantaged and vulnerable groups.

In this study the investigators will evaluate the effectiveness of already implemented in-person cessation interventions targeting smoking, use of snus and/or e-cigarettes, focusing on disadvantaged and vulnerable groups of tobacco users. Furthermore, important factors associated with a successful outcome after controlling for confounders will be identified (in relation to programme, patients and setting).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All adult tobacco users (of at least 18 years of age), including disadvantaged and vulnerable patients, receiving an in-person intervention (incl. online meetings) for tobacco cessation (smoking, snus and/or e-cigarettes) are eligible for inclusion in the project after giving informed consent.
  • Both individual and group-based interventions can be included.

排除标准

  • Withdrawing consent.
  • Reduced ability to give informed consent, due to inadequate language skills, dementia, and other conditions.

结局指标

主要结局

% of patients that are continuously smokefree

时间窗: 6 months

Self-reported smoking status, questionnaire completed by telephone interview

次要结局

  • % of patients that are smokefree(On completion of the tobacco cessation programme (app. 1 month after quitting))
  • % of patients that have been smokefree for at least the latest 14 days(6 months)
  • % of patients that are satisfied with the smoking cessation intervention(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hanne Tonnesen

Professor

Lund University

研究点 (8)

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