跳至主要内容
临床试验/NL-OMON47612
NL-OMON47612已完成4 期

Advancing addiction treatment using neuromodulation: a rTMS enhanced CBT trial - Advancing addiction treatment

Academisch Medisch Centrum0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
80

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

  • The recruitment of participants will take place as follows. Practitioners at
  • Jellinek will inform patients about our study and we will give presentations at
  • Jellinek to inform patients about this study. If somebody is willing to
  • participate in the study, we will personally visit them at Jellinek and explain
  • the entire procedure. Furthermore they will receive an information letter by
  • email to make sure they can read the information again carefully. If they are
  • still interested in participation they will sign informed consent and we will
  • perform screening for inclusion and exclusion criteria. Demographics,
  • psychiatric disorders (MINI), TMS contraindications and MR contraindications
  • are questioned to make sure that the individual can participate.
  • If a participant meets any of the exclusion criteria that they are excluded
  • from participation in this study. , Inclusion criteria
  • - Men and women.
  • - Age between 25-65.
  • - Recent DSM-V diagnosis (mild, moderate and severe) of alcohol abuse (<4
  • months after detox).
  • - Currently in treatment (>3 weeks after detox) and will be in treatment during
  • the entire stimulation period (2 weeks after inclusion).
  • - Sufficient speaking and understanding of Dutch language.

排除标准

  • Exclusion criteria
  • - A DSM-V diagnosis of schizophrenia or another psychotic disorder, personality
  • disorder or sleep disorder.
  • - TMS contraindications: history of epileptic seizures or epilepsy in a first
  • degree relative, irregular sleep/ wake rhythm.
  • - MR contraindications (only relevant for the 40 participants who will undergo
  • MR scanning): metal implants, claustrophobia.

研究者

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