Baldofski Sabrina, Kohls Elisabeth, Bauer Stephanie, Becker Katja, Bilic Sally, Eschenbeck Heike, Kaess Michael, Moessner Markus, Salize Hans Joachim, Diestelkamp Silke, Voß Elke, Rummel-Kluge Christine
Department of Psychiatry and Psychotherapy, Medical Faculty, University Leipzig, Semmelweisstraße 10, 04103, Leipzig, Germany.
Center for Psychotherapy Research, University Hospital Heidelberg, Heidelberg, Germany.
Trials. 2019 Jan 15;20(1):53. doi: 10.1186/s13063-018-3156-8.
Depression is a serious mental health problem and is common in children and adolescents. Online interventions are promising in overcoming the widespread undertreatment of depression and in improving the help-seeking behavior in children and adolescents.
The multicentre, randomized controlled E.motion trial is part of the German ProHEAD consortium (Promoting Help-seeking using E-technology for ADolescents). The objective of the trial is to investigate the efficacy and cost-effectiveness of two online interventions to reduce depressive symptomatology in high-risk children and adolescents with subsyndromal symptoms of depression in comparison to an active control group. Participants will be randomized to one of three conditions: (1) Intervention 1, a clinician-guided self-management program (iFightDepression®); (2) Intervention 2, a clinician-guided group chat intervention; and (3) Control intervention, a psycho-educational website on depressive symptoms. Interventions last six weeks. In total, N = 363 children and adolescents aged ≥ 12 years with Patient Health Questionnaire-9 modified for Adolescents (PHQ-A) scores in the range of 5-9 will be recruited at five study sites across Germany. Online questionnaires will be administered before onset of the intervention, at the end of the intervention, and at the six-month follow-up. Further, children and adolescents will participate in the baseline screening and the one- and two-year school-based follow-up assessments integrated in the ProHEAD consortium. The primary endpoint is depression symptomatology at the end of intervention as measured by the PHQ-A score. Secondary outcomes include depression symptomatology at all follow-ups, help-seeking attitudes, and actual face-to-face help-seeking, adherence to and satisfaction with the interventions, depression stigma, and utilization and cost of interventions.
This study represents the first randomized controlled trial (RCT) investigating efficacy and cost-effectiveness of two online interventions in children and adolescents aged ≥ 12 years at risk for depression. It aims to provide a better understanding of the help-seeking behavior of children and adolescents, potential benefits of E-mental health interventions for this age group, and new insights into so far understudied aspects of E-mental health programs, such as potential negative effects of online interventions. This knowledge will be used to tailor and improve future help offers and programs for children and adolescents and ways of treatment allocation.
German Register for Clinical Trials (DRKS), DRKS00014668 . Registered on 4 May 2018. International trial registration took place through the "international clinical trials registry platform" with the secondary ID S-086/2018.
抑郁症是一个严重的心理健康问题,在儿童和青少年中很常见。在线干预在克服抑郁症普遍治疗不足以及改善儿童和青少年的求助行为方面很有前景。
多中心随机对照E.motion试验是德国ProHEAD联盟(利用电子技术促进青少年求助)的一部分。该试验的目的是研究两种在线干预措施与一个积极对照组相比,在减少有亚综合征性抑郁症状的高危儿童和青少年抑郁症状方面的疗效和成本效益。参与者将被随机分配到三种情况之一:(1)干预1,一个由临床医生指导的自我管理项目(iFightDepression®);(2)干预2,一个由临床医生指导的群组聊天干预;(3)对照干预,一个关于抑郁症状的心理教育网站。干预持续六周。总共将在德国的五个研究地点招募N = 363名年龄≥12岁、青少年版患者健康问卷-9(PHQ-A)得分在5至9分之间的儿童和青少年。在线问卷将在干预开始前、干预结束时以及六个月随访时进行。此外,儿童和青少年将参与ProHEAD联盟整合的基线筛查以及一年和两年的校内随访评估。主要终点是干预结束时用PHQ-A得分衡量的抑郁症状。次要结果包括所有随访时的抑郁症状、求助态度、实际面对面求助、对干预的依从性和满意度、抑郁污名以及干预的利用情况和成本。
本研究是第一项调查两种在线干预措施对年龄≥12岁有抑郁风险的儿童和青少年的疗效和成本效益的随机对照试验(RCT)。其目的是更好地了解儿童和青少年的求助行为、电子心理健康干预对该年龄组的潜在益处,以及对电子心理健康项目迄今研究不足的方面(如在线干预的潜在负面影响)的新见解。这些知识将用于定制和改进未来为儿童和青少年提供的帮助及项目以及治疗分配方式。
德国临床试验注册中心(DRKS),DRKS00014668。于2018年5月4日注册。通过“国际临床试验注册平台”进行国际试验注册,二级编号为S-086 / 2018。