跳至主要内容
临床试验/NL-OMON47093
NL-OMON47093
招募中
不适用

The efficacy of Inquiry Based Stress Reduction (IBSR) for depression, <br>a randomized clinical trial. - IBSR for depression

FortaGroep0 个研究点目标入组 88 人待定

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
FortaGroep
入组人数
88
状态
招募中
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
2年前
研究类型
Interventional

研究者

发起方
FortaGroep

入排标准

入选标准

  • 1\. Patients will be eligible to participate if they meet the DSM\-IV (APA, 2000\) criteria for a major depressive disorder, mild to moderate, as the principal diagnosis on the Structured Clinical Interview for DSM\-IV Axis I Disorders \* Dutch version (SCID\-I; van Groenestijn, et al., 1998\).
  • 2\. Aged 18 years and older
  • 3\. Not making use of other treatment for depression at the time
  • 4\. No history of psychotherapy in the last year
  • 5\. No medication for depression or unchanged dosage of medication during the last two months
  • 6\. All participants must be willing to refrain from engaging in additional psychological treatments or making changes to their medication status during the course of the trial. (changes in medication dosage will result in dropout)
  • 7\. All participants are required to have sufficient knowledge of the Dutch language

排除标准

  • Patients will only be excluded if they:
  • 1\. have active suicidal intent (which is asked during the interviews and further operationalized with help of the ninth item in the BDI\-II\-NL at pre\-treatment: If patients marked the statement \*\*I would kill myself if I could\*\*, they are classified as being at risk of suicide),
  • 2\. meet the DSM\-IV\-TR criteria for severe major depressive disorder, psychotic disorder, or bipolar disorder,
  • 3\. suffer from mental impairment or neurocognitive disorders such as Alzheimer,
  • 4\. have substance abuse requiring specialist treatment,
  • 5\. have no time for homework.

结局指标

主要结局

未指定

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