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基于电话干预对重度精神障碍患者戒烟的有效性:一项随机对照试验的研究方案

Effectiveness of a telephone-based intervention for smoking cessation in patients with severe mental disorders: study protocol for a randomized controlled trial.

作者信息

Ballbè Montse, Martínez Cristina, Feliu Ariadna, Torres Núria, Nieva Gemma, Pinet Cristina, Raich Antònia, Mondon Sílvia, Barrio Pablo, Hernández-Ribas Rosa, Vicens Jordi, Costa Sílvia, Vilaplana Jordi, Alaustre Laura, Vilalta Eva, Blanch Roser, Subirà Susana, Bruguera Eugeni, Suelves Josep Maria, Guydish Joseph, Fernández Esteve

机构信息

Tobacco Control Unit, Cancer Control and Prevention Program, Institut Català d'Oncologia-ICO, Av. Granvia de L'Hospitalet 199-203, L'Hospitalet de Llobregat, 08908, Barcelona, Spain.

Cancer Control and Prevention Group, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, Av. Granvia de L'Hospitalet 199-203, L'Hospitalet de Llobregat, 08908, Barcelona, Spain.

出版信息

Trials. 2019 Jan 11;20(1):38. doi: 10.1186/s13063-018-3106-5.

Abstract

BACKGROUND

Up to 75% of inpatients with mental disorders smoke, and their life expectancy is decreased by up to 25 years compared to the general population. Hospitalized patients without monitoring after discharge quickly return to prehospitalization levels of tobacco use. The aim of the 061 QuitMental study is to assess the effectiveness of a multicomponent and motivational telephone-based intervention to stop smoking through a quitline addressed to smokers discharged from mental health hospital wards.

METHODS

A pragmatic randomized controlled trial, single blinded, will include 2:1 allocation to the intervention group (IG) and the control group (CG). The IG will receive telephone assistance to quit smoking (including psychological and psychoeducational support, and pharmacological treatment advice if required) proactively for 12 months, and the CG will receive only brief advice after discharge. The sample size, calculated with an expected difference of 15 points on smoking abstinence between groups (IG, 20% and CG, 5%), α = 0.05, β = 0.10, and 20% loss, will be 334 participants (IG) and 176 participants (CG). Participants are adult smokers discharged from psychiatric units of five acute hospitals. Measurements include dependent variables (self-reported 7-day point prevalence smoking abstinence (carbon monoxide verified), duration of abstinence, number of quit attempts, motivation, and self-efficacy to quit) and independent variables (age, sex, and psychiatric diagnoses). In data analysis, IG and CG data will be compared at 48 h and 1, 6, and 12 months post discharge. Multivariate logistic regression (odds ratio; 95% confidence interval) of dependent variables adjusted for potential confounding variables will be performed. The number needed to treat to achieve one abstinence outcome will be calculated. We will compare the abstinence rate of enrolled patients between groups.

DISCUSSION

This trial evaluates an innovative format of a quitline for smokers with severe mental disorders regardless of their motivation to quit. If effective, the pragmatic nature of the study will permit transfer to routine clinical practice in the National Health System.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT03230955 . Registered on 24 July 2017.

摘要

背景

高达75%的精神障碍住院患者吸烟,与普通人群相比,他们的预期寿命缩短了25年。出院后未接受监测的住院患者很快就会恢复到住院前的吸烟水平。061戒烟心理研究的目的是评估一种多成分、基于动机的电话干预措施通过面向从精神科病房出院的吸烟者的戒烟热线来戒烟的有效性。

方法

一项实用的单盲随机对照试验,将按2:1的比例分配到干预组(IG)和对照组(CG)。干预组将在12个月内主动接受戒烟电话援助(包括心理和心理教育支持,以及必要时的药物治疗建议),对照组在出院后仅接受简短建议。根据两组戒烟率预期相差15个百分点(干预组20%,对照组5%)、α = 0.05、β = 0.10以及20%的失访率计算得出,样本量将为334名参与者(干预组)和176名参与者(对照组)。参与者为来自五家急症医院精神科病房的成年吸烟者。测量指标包括因变量(自我报告的7天点患病率戒烟情况(经一氧化碳验证)、戒烟持续时间、戒烟尝试次数、动机以及戒烟自我效能感)和自变量(年龄、性别和精神科诊断)。在数据分析中,将在出院后48小时以及1、6和12个月时比较干预组和对照组的数据。将对因变量进行多因素逻辑回归分析(比值比;95%置信区间),并对潜在混杂变量进行校正。将计算实现一种戒烟结果所需的治疗人数。我们将比较两组中登记患者的戒烟率。

讨论

本试验评估了一种针对重度精神障碍吸烟者的创新型戒烟热线形式,无论其戒烟动机如何。如果有效,该研究的实用性将使其能够推广至国家卫生系统的常规临床实践中。

试验注册

ClinicalTrials.gov,NCT03230955。于2017年7月24日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d89/6329054/96b2a4a6cefe/13063_2018_3106_Fig1_HTML.jpg

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