跳至主要内容
临床试验/DRKS00030915
DRKS00030915招募中4 期

Single-case prediction of treatment (non-) response to cognitive-behavioral therapy (CBT) in the outpatient sector: a prospective-longitudinal observational study - TiKi-Study

Humboldt-Universität zu Berlin0 个研究点目标入组 585 人开始时间: 2022年12月17日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
585

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Inclusion criteria are: a primary diagnosis according to DSM-5 of specific phobia (SP), social anxiety disorder (SAD), panic disorder (PD), agoraphobia (AG), generalized anxiety disorder (GAD), obsessive-compulsive disorder (OCD), posttraumatic stress disorder (PTSD), unipolar depressive disorder (major depression or dysthymia, DD), age = 18, indication for outpatient CBT treatment, treatment dose of at least 12 sessions (excluding probatory sessions; 12 sessions is a minimal fixed dose of short-term treatment in the German health care system), symptom severity as indicated by a General Severity Index of the Brief Symptom Inventory (BSI-GSI) > 0.56 and a Clinical Global Impression – Severity Scale (CGI-S) score = 3 (mildly ill), willingness to participate in this study. Fostering ecological validity, exclusion criteria will be kept to a minimum.

排除标准

  • We will exclude patients with a current secondary diagnosis of moderate to severe substance use disorder (including regular use of benzodiazepines), psychosis, bipolar disorder, acute suicidality and medical conditions as contraindication for CBT. Other comorbid disorders from the internalizing spectrum are not excluded. If outpatient treatment is interrupted due to inpatient treatment, patients will be excluded. Concurrent pharmacological treatment is not followed by exclusion, but will be documented in detail.

研究者

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