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Completed

NCT Number: NCT02841683

Pragmatic Randomised Controlled Trial Evaluating Effectiveness of a Smoking Cessation e- Intervention " Tabac Info Service "

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

université de Bordeaux

Bordeaux, 33000, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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).

Exclusion criteria

  • refusal to participate in the study

Treatment and study plan

Tabac Info Service

Behavioral

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

Primary outcomes

  1. Point prevalence abstinence of 7 days

    Time frame: 6 months

Secondary outcomes

  1. continuous abstinence rate

    Time frame: 6 months

    Defined as the proportion of participants remaining continuously abstinent from the cessation date to the endpoint

  2. continuous abstinence rate

    Time frame: 12 months

    Defined as the proportion of participants remaining continuously abstinent from the cessation date to the endpoint

  3. minimum 24-hour point abstinence

    Time frame: 3 months

  4. minimum 30-day point abstinence

    Time frame: 12 months

  5. number of quit attempts

    Time frame: 6 months

  6. total duration of quit attempts

    Time frame: 6 months

    calculated as sum of days with no use

Sponsors and collaborators

Lead sponsor

Ecole des Hautes Etudes en Santé Publique

Other

Registry information

Official study title

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

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 22, 2016
Registry last updated
Aug 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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