Efficacy of a transdiagnostic Internet prevention approach in adolescents (EMPATIA study): study protocol of a randomized controlled trial.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Anja Hirsig, Xenia Anna Häfeli, Stefanie Julia Schmidt
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引用次数: 0

Abstract

Background: Most mental disorders have their onset in adolescence. Preventive interventions during this period are important; however, help-seeking behavior is generally poor in this age group resulting in low treatment rates. Internet interventions are expected to be an effective, low-threshold, and scalable approach to overcome barriers to help-seeking, particularly for individuals experiencing subclinical symptoms. Internet-delivered indicated prevention seems promising as it targets individuals with minimal symptoms of mental disorders who might need care but are not help-seeking yet. Previous indicated prevention-approaches have mainly targeted specific risk-syndromes. However, this contradicts the increasing recognition of emerging psychopathology as a complex system characterized by co-occurrence and rapid shifts of subclinical symptoms cutting across diagnostic categories. Therefore, this study will investigate the efficacy, mediators, moderators, and core symptomatic changes of a transdiagnostic Internet-delivered indicated prevention program (EMPATIA program) for adolescents.

Methods: This randomized controlled trial (RCT) will be conducted in a general population sample (planned n = 152) of adolescents aged 12-18 years with subclinical symptoms but without any current or past mental disorder. Participants will be randomly assigned to the EMPATIA program or a care as usual (CAU) control condition. The 8-week guided EMPATIA program encompasses 8 modules targeting the following transdiagnostic mechanisms: repetitive negative thinking, self-perfectionism, emotion regulation, intolerance of uncertainty, rejection sensitivity, and behavioral avoidance. Participants will be asked to answer online self-report questionnaires at baseline, after 8 weeks, and at 6-, 9-, and 12-month follow-up. Diagnostic telephone interviews will be conducted at baseline and at 12-month follow-up. Additionally, intervention-specific constructs (motivation, alliance, negative effects, satisfaction, adherence) will be assessed during and after the EMPATIA program. The level of self-reported general psychopathology post-intervention is the primary outcome.

Discussion: Results will be discussed considering the potential of Internet interventions as a scalable, low-threshold option for indicated prevention in adolescents experiencing subclinical symptoms. The EMPATIA program introduces a novel Internet prevention program targeting six transdiagnostic mechanisms associated with various mental health outcomes. Thereby, this trial pursues a very timely and important topic because it may contribute to narrow the current care gap for adolescents, to prevent mental health problems and related negative consequences, and to promote mental health in the long-term.

Trial registration: The trial was approved by Swissmedic (Registration Number: 10001035, 08/22/2022) and the Ethics Committee of Bern (Registration Number: 2022-D0036, 08/22/2022). The trial was registered at ClinicalTrials.gov NCT05934019 on 07-03-2023.

青少年跨诊断互联网预防方法的功效(EMPATIA 研究):随机对照试验研究方案。
背景:大多数精神疾病都是在青少年时期发病的。在这一时期采取预防性干预措施非常重要;然而,这一年龄组的求助行为普遍较差,导致治疗率较低。互联网干预有望成为一种有效、低门槛、可扩展的方法,以克服求助障碍,尤其是对于出现亚临床症状的个人。互联网提供的指示性预防似乎很有前景,因为它针对的是精神障碍症状轻微、可能需要治疗但尚未寻求帮助的人。以往的指示性预防方法主要针对特定的风险综合征。然而,这与人们日益认识到的新出现的精神病理学是一个复杂的系统相矛盾,其特点是亚临床症状的共同出现和快速转变,跨越了诊断类别。因此,本研究将调查一项针对青少年的跨诊断性互联网传播指示性预防计划(EMPATIA 计划)的疗效、中介因素、调节因素和核心症状变化:这项随机对照试验(RCT)将在具有亚临床症状但目前或过去没有任何精神障碍的 12-18 岁青少年中的普通人群样本(计划人数 = 152)中进行。参与者将被随机分配到 EMPATIA 项目或照常护理(CAU)对照组。为期 8 周的 EMPATIA 指导课程包括 8 个模块,针对以下跨诊断机制:重复性消极思维、自我完美主义、情绪调节、不确定性不容忍、拒绝敏感性和行为回避。参与者将在基线、8 周后、6 个月、9 个月和 12 个月的随访中回答在线自我报告问卷。在基线和 12 个月随访时,将进行诊断性电话访谈。此外,在 EMPATIA 计划期间和之后,还将对干预的特定结构(动机、联盟、负面影响、满意度、坚持性)进行评估。干预后自我报告的一般精神病理学水平是主要结果:讨论:考虑到互联网干预作为一种可扩展、低门槛的选择,对出现亚临床症状的青少年进行预防的潜力,将对结果进行讨论。EMPATIA 计划引入了一种新型互联网预防计划,针对与各种心理健康结果相关的六种跨诊断机制。因此,这项试验是一个非常及时和重要的课题,因为它可能有助于缩小目前对青少年的护理差距,预防心理健康问题和相关的负面影响,并促进长期的心理健康:该试验获得了瑞士医疗机构(注册号:10001035,2022年8月22日)和伯尔尼伦理委员会(注册号:2022-D0036,2022年8月22日)的批准。该试验于 2023 年 3 月 7 日在 ClinicalTrials.gov NCT05934019 上注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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