针对儿童和青少年及其家庭的神经性厌食症家庭治疗(HoT 研究):随机、对照、多中心、开放标签、平行小组优越性试验的研究方案。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-11-13 DOI:10.1186/s13063-024-08566-z
Brigitte Dahmen, Ingar Zielinski-Gussen, Manuel Föcker, Freia Hahn, Tanja Legenbauer, Ulf Thiemann, Astrid Dempfle, Beate Herpertz-Dahlmann
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引用次数: 0

摘要

背景:改善神经性厌食症(AN)儿童和青少年的预后迫切需要新的治疗方法。最近,研究人员对患者父母/照顾者积极参与的多学科家庭治疗的可行性进行了调查。然而,与住院治疗等标准治疗方法相比,目前还没有进行过相关的临床试验来检验这种方法的有效性和安全性:在这项多中心随机对照试验中,德国5家主要的AN治疗中心为12至18岁的儿童和青少年AN患者提供了家庭治疗。约240名因自闭症入院的患者将被纳入试验范围。经过短暂的住院躯体稳定期(5-8周)后,患者被随机分配接受常规治疗(TAU),即继续住院治疗或日间治疗,或接受新开发的家庭治疗(HoT)(每组82人,共164人)。整个治疗过程中有三次评估(入院、随机化和出院),以及入院后 9 个月和 12 个月的随访评估。入院后 12 个月时的体重指数(主要结果)在各组之间进行比较(根据入院前的体重指数和入院时的体重指数进行调整);次要结果包括饮食失调和一般心理病理学、精神病患者再次住院的次数和持续时间、生活质量、治疗动机和治疗满意度。其他次要结果包括主要护理人员处理儿童疾病的负担和技能以及直接治疗费用。统计分析将基于意向治疗原则,使用混合模型进行重复测量。(在整个治疗过程中将对(严重)不良事件进行评估。此外,还将评估 HoT 的可行性和实施情况,以及两组多学科治疗小组成员的满意度和工作量:讨论:如果评估结果良好,HoT可被视为一种有效的治疗方法,可替代或完善IP等既有的治疗方法,用于治疗儿童和青少年的AN。家庭治疗环境可缩短这一患者群体的住院时间,提高治疗满意度,并有助于降低再次住院的风险,这与这一易感患者群体的较佳治疗效果有关:该试验于2021年11月26日在德国临床试验注册中心(DRKS)注册,注册号为DRKS00025925(前瞻性注册):https://drks.de/search/de/trial/DRKS00025925 。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anorexia nervosa-specific home treatment in children and adolescents and their families (the HoT study): a study protocol of a randomized, controlled, multicenter, open-label, parallel group superiority trial.

Background: New treatment approaches are urgently needed to improve the prognosis of children and adolescents with anorexia nervosa (AN). Recently, the feasibility of multidisciplinary home treatment that strongly involves the patients' parents/caregivers has been investigated. However, no RCT has yet been performed to test the efficacy and safety of this approach compared to standard treatment approaches, such as inpatient treatment.

Methods: In this multicenter randomized-controlled trial, home treatment for children and adolescents with AN aged 12 to 18 years is established at 5 major treatment centers for AN in Germany. Approximately 240 patients who are admitted to the hospital for AN will be included in the trial. After a short inpatient somatic stabilization phase (5-8 weeks), patients are randomized to receive either treatment as usual (TAU), in the form of continued inpatient or day patient treatment, or the newly developed home treatment (HoT) (n = 82/arm, n = 164 in total). There are three assessments throughout treatment (admission, randomization, and discharge), as well as follow-up assessments at 9 and 12 months after admission. The BMI at 12 months after admission (primary outcome) is compared between groups (adjusted for premorbid BMI and admission BMI); secondary outcomes include eating disorder and general psychopathology, the number and duration of psychiatric rehospitalizations, quality of life, motivation for treatment and treatment satisfaction. Other secondary outcomes include the primary caregivers' burden and skills in handling the child's illness and direct treatment costs. Statistical analysis will be based on intention-to-treat principles, using mixed models for repeated measures. (Serious) adverse events are assessed throughout treatment. In addition, the feasibility and implementation of HoT as well as the satisfaction and workload of the members of the multidisciplinary treatment teams in both arms will be assessed.

Discussion: In the case of a positive evaluation, HoT can be considered an effective treatment method to replace or complete established treatment methods, such as IP, for treating AN in children and adolescents. The home treatment setting might shorten inpatient stays in this patient group, increase treatment satisfaction, and help to reduce the risk of rehospitalization, which is associated with a better outcome in this vulnerable patient group.

Trial registration: The trial was registered with the German Clinical Trial Register (DRKS) under the ID DRKS00025925 on November 26, 2021 (prospectively registered): https://drks.de/search/de/trial/DRKS00025925 .

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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