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临床试验/NCT04765813
NCT04765813已完成不适用

A Randomized Clinical Trial to Assess the Efficacy of a Psychological Treatment to Quit Smoking Assisted With an App

University of Santiago de Compostela2 个研究点 分布在 1 个国家目标入组 287 人开始时间: 2021年9月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
287
试验地点
2
主要终点
Point-prevalence abstinence

研究概览

简要总结

This randomized controlled clinical trial examines the effectiveness of a face-to-face* cognitive-behavioral behavioral treatment to quit smoking enriched with an App. This project aims to innovate in the psychological smoking cessation treatment and increase abstinence rates in the short and long term.

* Due to the COVID-19 the face-to-face treatment will be conducted in an online format.

详细描述

Psychological treatment (cognitive-behavioral) is a first-line smoking cessation treatment that has proven its efficacy. However, it is necessary to continue investigating to improve smoking outcomes as abstinence and reduce relapse rates. The use of information technologies (ICTs) in the field of health has grown and developed significantly in recent years. Specifically, mobile applications (Apps), aimed at different health-related aspects (mHealth Apps), are a valuable resource. Its use, as a complement to the face-to-face treatment, could help to increase motivation to quit smoking, treatment adherence, and therapeutic activities compliance.

mHealth Apps are becoming highly relevant due to their cost-effectiveness and the added attractiveness for many users. Considering this context, the main aim of the present project is to design and assess the efficacy of a cognitive-behavioral treatment (CBT) for smoking cessation enriched with a Smartphone App.

A randomized clinical trial will be carried out with a sample of 270 treatment-seeking smokers at the Smoking Cessation and Addictive Disorders Unit of the University of Santiago de Compostela. Participants will be randomly assigned to one of the following groups:

  1. The experimental group (CBT + App), in which participants will receive a cognitive-behavioral treatment* to quit smoking along with an App with active therapeutic components during the treatment and 12 months follow-ups period (n = 135)
  2. The control group (CBT), in which participants will receive the same cognitive-behavioral treatment* along with the use of a Control App (without active components) during the treatment (n = 135).

The main hypothesis is that the combination of a cognitive-behavioral psychological treatment to quit smoking and an App with active therapeutic components will obtain higher abstinence rates at the end of treatment and the 12-month follow-up period, compared to the control group

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

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

  • 18 years of age or older who smoke at least 8 cigarettes per day
  • Desire to participate voluntarily in the treatment offered to quit smoking
  • Correctly fill out all the pretreatment assessment questionnaires
  • Be able to provide written informed consent
  • Currently own a valid email and a smartphone Android or iOS and willing to use it during treatment

排除标准

  • To have a diagnosis of a severe mental disorder (bipolar disorder and/or psychotic disorder)
  • To have a substance use disorder (alcohol, cannabis, cocaine, heroin), different from a tobacco use disorder
  • To smoke rolling snuff, cigars, little cigars, or other tobacco products
  • To have participated in an effective psychological treatment to quit smoking during the previous 12 months
  • To have received other effective pharmacological treatment to quit smoking in the previous 12 months (nicotine gum or patches, bupropion, varenicline)
  • To have a physical pathology involving life-threatening risks for the person who would require immediate intervention in individual format (e.g., recent myocardial infarction, pneumothorax)
  • To have a visual impairment that impedes the use of the App

结局指标

主要结局

Point-prevalence abstinence

时间窗: 1 year

Participants will be considered abstinent if they report abstinence, not even a puff of a cigarette, for ≥7 days at the end of treatment (week 8 since beginning treatment), and prior to follow-up day at 3-, 6-, and 12-months follow-up.

次要结局

  • Reduction of cigarette consumption (cigarettes per day)(1 year)
  • Continuous abstinence(1 year)

研究者

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

Elisardo Becoña Iglesias

Professor of Clinical Psychology at the Faculty of Psychology

University of Santiago de Compostela

研究点 (2)

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