DRKS00013769招募中3 期
Cognitive behavioural therapy for the treatment of late life depression – a multicentre, randomized, observer- blinded, controlled trial (CBTlate) - CBTlate
niversitätsklinikum Köln Klinik für Psychiatrie und Psychotherapie0 个研究点目标入组 248 人开始时间: 2018年6月28日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 248
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
- Randomized controlled study
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 60 Years 至 one(—)
- 性别
- All
入选标准
- •1. out-patient status
- •2. male/ female, age = 60 years inclusive at screening
- •3. depressive episode (moderate to severe according to ICD-10)
- •4. Geriatric Depression Scale (GDS) > 10
- •5. Quick Inventory of Depressive Symptomatology (QIDS-C > 10)
- •6. MMSE > 25 points
- •7. no or stable (= 6 weeks) antidepressive pharmacological treatment at baseline and stable antidepressive pharmacological treatment during 8-week intervention
- •8. sufficient German language skills
- •9. written informed consent signed
排除标准
- •Bipolar depression
- •Schizophrenia
- •Other psychotic disorders
- •Substance abuse or dependency
- •Acute suicidality
- •Anxiety disorder as stand-alone diagnosis (e.g. generalized anxiety disorder, panic disorder, phobia)
- •Obsessive-compulsive disorder as stand-alone diagnosis
- •Participation in another trial of psychotherapeutic/psychiatric intervention parallel to this trial
- •Additional psychological/ psychotherapeutic treatment throughout the study including the follow- up visit
- •Regular use with scheduled dosing of Benzodiazepines (not PRN)
- •Severe or instable medical condition, which clearly impacts on depression or on the ability to participate in the trial
- •Brain disease with severe functional impairement that impacts the ability to participate in the trial (e.g. aphasia, Parkinson’s disease)
研究者
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