跳至主要内容
临床试验/NL-OMON39268
NL-OMON39268招募中不适用

Trial Illness Management and Recovery (IMR) Effects of IMR on patients with severe mental illness - Trial IMR

Parnassia Bavo Groep (Den Haag)0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Patients with serious and persistent psychiatric illnesses. Most of them will be patients who have a psychotic disorder, schizoaffective disorders or bipolar disorders with or without comorbid disorders (such as substance abuse and personality disorders)
  • - The patient is treated on an outpatient basis
  • - Written informed consent

排除标准

  • - Having done an IMR-training
  • - Organic brain syndrome.
  • - Incompetence regarding the giving of informed consent.
  • - Patients with severe cognitive impairments who are unable to follow the training
  • - Insufficient knowledge of the Dutch language (they can not participate in the group)

研究者

发起方
Parnassia Bavo Groep (Den Haag)

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