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一项平行组随机临床试验的统计分析计划,该试验比较了图式疗法与常规治疗对难治性抑郁症门诊患者的疗效(DEPRE-ST)。

Statistical analysis plan for a parallel group randomized clinical trial comparing schema therapy versus treatment as usual for outpatients with difficult-to-treat depression (DEPRE-ST).

作者信息

Arendt Ida-Marie T P, Gondan Matthias, Juul Sophie, Hastrup Lene Halling, Hjorthøj Carsten, Moeller Stine B

机构信息

Department of Psychology, University of Southern Denmark, Campusvej 55, 5230, Odense, Denmark.

Department of Interdisciplinary Trauma Treatment, Mental Health Services in the Region of Southern Denmark, Østre Hougvej 55, 5500, Middelfart, Denmark.

出版信息

Trials. 2025 Sep 1;26(1):334. doi: 10.1186/s13063-025-09012-4.

Abstract

BACKGROUND

"Difficult-to-treat" depression - here operationalized as either chronic or treatment-resistant depression - encompasses about one third of all patients with depression. Despite its considerable size, the patient group is understudied, and evidence-based psychotherapeutic treatment options are currently limited. The DEPRE-ST trial therefore seeks to investigate beneficial and harmful effects of schema therapy for difficult-to-treat depression.

METHODS

This is a randomized multicenter parallel-group superiority clinical trial. A total of 129 patients will be randomized to receive either 30 sessions of individual schema therapy or psychotherapy according to Treatment As Usual, along with psychopharmacological treatment. Participants are assessed before randomization and at 6, 12, and 24 months after randomization. The primary outcome is depression symptoms (6-item Hamilton Rating Scale for Depression), assessed at 12 months. Secondary outcomes include health-related quality of life (European Quality of Life 5 Dimensions 5 Level Version), functional impairment (Work and Social Adjustment Scale), psychological wellbeing (WHO-5 Well-being Index), and negative effects of treatment (Negative Effects Questionnaire), alongside a range of patient-relevant exploratory outcomes. Blinding of treatment allocation is ensured for primary outcome assessors, statisticians, and the data safety and monitoring committee. The primary outcome will be analyzed with multilevel linear regression, with conservative multiple imputation for missing data, and presented as the covariate-adjusted difference between treatments' change scores with its 95% confidence intervals. Further, a health economic analysis will be performed.

DISCUSSION

This statistical analysis plan was developed and submitted before unblinding of data to ensure transparency and diminish bias in selection, analysis, and reporting of results.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05833087. Registered on 15th April 2023. https://clinicaltrials.gov/study/NCT05833087?term=depre-st&checkSpell=false&rank=1.

摘要

背景

“难治性”抑郁症(此处定义为慢性或难治性抑郁症)约占所有抑郁症患者的三分之一。尽管这一患者群体规模较大,但目前对其研究不足,且循证心理治疗选择有限。因此,DEPRE-ST试验旨在研究图式疗法对难治性抑郁症的有益和有害影响。

方法

这是一项随机多中心平行组优效性临床试验。总共129名患者将被随机分配,接受30次个体图式疗法或常规治疗下的心理治疗,并同时接受心理药物治疗。在随机分组前以及随机分组后6个月、12个月和24个月对参与者进行评估。主要结局是在12个月时评估的抑郁症状(6项汉密尔顿抑郁评定量表)。次要结局包括健康相关生活质量(欧洲生活质量5维度5水平版本)、功能损害(工作和社会适应量表)、心理健康(WHO-5幸福指数)和治疗的负面影响(负面影响问卷),以及一系列与患者相关的探索性结局。主要结局评估者、统计学家以及数据安全和监测委员会将确保治疗分配的盲法。主要结局将采用多水平线性回归分析,对缺失数据进行保守多重插补,并以治疗组变化分数的协变量调整差异及其95%置信区间呈现。此外,还将进行健康经济分析。

讨论

本统计分析计划是在数据未揭盲前制定并提交的,以确保透明度并减少结果选择、分析和报告中的偏差。

试验注册

ClinicalTrials.gov NCT05833087。于2023年4月15日注册。https://clinicaltrials.gov/study/NCT05833087?term=depre-st&checkSpell=false&rank=1

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