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首页> 外文期刊>BMC Psychiatry >Cost-effectiveness of i-Sleep, a guided online CBT intervention, for patients with insomnia in general practice: protocol of a pragmatic randomized controlled trial
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Cost-effectiveness of i-Sleep, a guided online CBT intervention, for patients with insomnia in general practice: protocol of a pragmatic randomized controlled trial

机译:i-Sleep(一种在线CBT指导性在线干预)在一般失眠患者中的成本效益:一项实用的随机对照试验方案

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摘要

Background Insomnia is a highly prevalent disorder causing clinically significant distress and impairment. Furthermore, insomnia is associated with high societal and individual costs. Although cognitive behavioural treatment for insomnia (CBT-I) is the preferred treatment, it is not used often. Offering CBT-I in an online format may increase access. Many studies have shown that online CBT for insomnia is effective. However, these studies have all been performed in general population samples recruited through media. This protocol article presents the design of a study aimed at establishing feasibility, effectiveness and cost-effectiveness of a guided online intervention (i-Sleep) for patients suffering from insomnia that seek help from their general practitioner as compared to care-as-usual. Methods/design In a pragmatic randomized controlled trial, adult patients with insomnia disorder recruited through general practices are randomized to a 5-session guided online treatment, which is called “i-Sleep”, or to care-as-usual. Patients in the care-as-usual condition will be offered i-Sleep 6?months after inclusion. An ancillary clinician, known as the psychological well-being practitioner who works in the GP practice (PWP; in Dutch: POH-GGZ), will offer online support after every session. Our aim is to recruit one hundred and sixty patients. Questionnaires, a sleep diary and wrist actigraphy will be administered at baseline, post intervention (at 8?weeks), and at 6?months and 12?months follow-up. Effectiveness will be established using insomnia severity as the main outcome. Cost-effectiveness and cost-utility (using costs per quality adjusted life year (QALY) as outcome) will be conducted from a societal perspective. Secondary measures are: sleep diary, daytime consequences, fatigue, work and social adjustment, anxiety, alcohol use, depression and quality of life. Discussion The results of this trial will help establish whether online CBT-I is (cost-) effective and feasible in general practice as compared to care-as-usual. If it is, then quality of care might be increased because implementation of i-Sleep makes it easier to adhere to insomnia guidelines. Strengths and limitations are discussed. Trial registration Netherlands Trial register NTR 5202 (registered April 17st 2015).
机译:背景失眠症是一种高度流行的疾病,引起临床上明显的困扰和损害。此外,失眠与高昂的社会和个人成本相关。尽管认知行为治疗失眠症(CBT-1)是首选治疗方法,但并不经常使用。以在线格式提供CBT-I可能会增加访问权限。许多研究表明,在线CBT治疗失眠是有效的。但是,这些研究都是在通过媒体招募的普通人群样本中进行的。该协议文章提出了一项研究的设计,旨在确定与一般照护相比寻求失眠患者寻求全科医生帮助的在线指导干预(i-Sleep)的可行性,有效性和成本效益。方法/设计在一项务实的随机对照试验中,通过一般做法招募的成年失眠症患者被随机分配到5疗程指导的在线治疗(称为“ i-Sleep”)或照常护理。入院后6个月,将照常照常为患者提供i-Sleep睡眠。在全科医生诊所工作的一名辅助临床医生,被称为心理健康医生(PWP;荷兰语:POH-GGZ),将在每次会议之后提供在线支持。我们的目标是招募160名患者。在基线,干预后(8周),以及6个月和12个月的随访中,将进行问卷调查,睡眠日记和腕部活动记录。将以失眠的严重程度为主要结果来确定有效性。成本效益和成本效用(将每个质量调整生命年的成本(QALY)用作结果)将从社会角度进行。次要措施是:睡眠日记,白天后果,疲劳,工作和社会适应,焦虑,饮酒,抑郁和生活质量。讨论该试验的结果将有助于确定与常规照护相比,在线CBT-1在一般实践中是否(成本有效)可行。如果是这样,则可以提高护理质量,因为实施i-Sleep可以更轻松地遵守失眠指南。讨论了优点和限制。试用注册荷兰试用注册NTR 5202(2015年4月17日注册)。

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