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临床试验/NCT02841683
NCT02841683已完成不适用

Evaluation of Effectiveness of Tabac Info Service (EE-TIS)

Ecole des Hautes Etudes en Santé Publique1 个研究点 分布在 1 个国家目标入组 2,806 人开始时间: 2017年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
2,806
试验地点
1
主要终点
Point prevalence abstinence of 7 days

研究概览

简要总结

Introduction - A national smoking cessation E-intervention, called Tabac Info Service (TIS), was developed in France to provide an adapted web and mobile application support to smoking cessation for all adults smokers, with or without chronic diseases, who want to stop smoking. This paper presents the study protocol of the evaluation of the program. The primary objective of this evaluation is to assess the efficacy and efficacy conditions of eTIS. The secondary objectives are to 1) describe efficacy variations in regard to user characteristics, 2) analyze mechanisms and efficacy conditions of eTIS, through variations of use, social or environmental contextual factors likely to influence the efficacy of eTIS, and the behavior change techniques (BCTs).

Methods and analyses - The study design is a two-arm pragmatic randomized controlled trial including a process evaluation with at least 3000 participants randomized to the intervention or to the control arm (current practices presented in a non-interactive website). Inclusion criteria are: Adults, Smokers with an information and consent form completed, Getting a smartphone and using mobile applications, wanting stop to smoking in short, medium or long terms. The exclusion criterion is the refusal to participate in the study. The primary outcome is the point prevalence abstinence of 7 days at 6 months later. The secondary outcomes are: the point prevalence abstinence of 24 h at 3 months later, the point prevalence abstinence of 30 days at 12 months later, number of quit attempts during the study, progression of stages within the program (changes and duration in each stage). Data will be analyzed in Intention to treat (main analyze) and per protocol ways. A logistic regression will be carried out to estimate an OR [95% confidence interval] for efficacy. A multivariate multilevel analysis will explore the influence of patients' characteristics, social and environmental context, conditions of use and behavior change techniques on results.

Dissemination -The findings of this study will allow us to understand and characterize the efficacy of eTIS, and conditions of its efficacy, underlining psychological, sociological, environmental and contextual factors, which could influence the efficacy of this type of intervention on smokers. These findings will be disseminated through peer-reviewed journals, national and international conference presentations and public events.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •adult smokers
  • •with an information and consent form completed
  • •agreed to participate in the study
  • •get a Smartphone and be willing to use applications
  • •wanting stop smoking (in short, medium or long terms).

排除标准

  • •refusal to participate in the study

研究组 & 干预措施

Lifestyle counseling

Active Comparator

A smoking cessation E-intervention, Tabac Info Service (TIS), by website and mobile application

干预措施: Tabac Info Service (Behavioral)

Current practices

No Intervention

Current practices of smoking cessation in France

结局指标

主要结局

Point prevalence abstinence of 7 days

时间窗: 6 months

次要结局

  • minimum 30-day point abstinence(12 months)
  • minimum 24-hour point abstinence(3 months)
  • number of quit attempts(6 months)
  • total duration of quit attempts(6 months)
  • continuous abstinence rate(12 months)
  • continuous abstinence rate(6 months)

研究者

发起方
Ecole des Hautes Etudes en Santé Publique
申办方类型
Other
责任方
Principal Investigator
主要研究者

Linda Cambon

Professor

Ecole des Hautes Etudes en Santé Publique

研究点 (1)

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