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

机译:严重精神障碍患者对基于电话的干预措施的有效性:随机对照试验的研究方案

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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. 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. 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. ClinicalTrials.gov, NCT03230955 . Registered on 24 July 2017.
机译:高达75%的患有精神障碍烟雾的住院患者,与一般人群相比,预期的预期寿命减少了25岁。出院后住院患者没有监测,迅速恢复到烟草使用的前一级。 061探亲研究的目的是评估多组分和励志的基于电话的干预的有效性,以戒烟通过从精神卫生医院病房排放的吸烟者戒烟。务实的随机对照试验单一盲,将包括2:1分配给干预组(Ig)和对照组(CG)。 IG将接收电话援助,以戒烟(包括心理和心理教育支持,如果需要)12个月,CG将仅在出院后仅收到简短的建议。样品尺寸计算,在组(Ig,20%和Cg,5%)之间吸烟禁欲的预期差异为15点(Ig,20%和5%),α?= 0.05,β?=?0.10和20%的损失,将是334名参与者(IG)和176名参与者(CG)。参与者是从五个急性医院的精神病单位排出的成人吸烟者。测量包括依赖变量(自我报告的7天患病症吸烟(一氧化碳验证),禁欲持续时间,戒烟的次数,动机和戒烟的自我效力)和独立变量(年龄,性别和精神病诊断)。在数据分析中,Ig和CG数据将在48℃和1,6和12?月后进行比较。将执行对潜在混淆变量调整的依赖变量的多变量的多变量逻辑回归(差距; 95%置信区间)。将计算治疗禁止结果所需的数量。我们将比较群体之间注册患者的禁欲率。本次试验评估吸烟者戒烟的创新形式,无论其动机退出,都有严重的精神障碍。如果有效,该研究的务实性质将允许转移到国家卫生系统中的常规临床实践。 ClinicalTrials.gov,NCT03230955。 2017年7月24日注册。

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