NL-OMON47598撤回不适用
Adding rTMS to exposure therapy in PTSD in a placebo-controlled design : a pilot study - rTMS in PTSD
试验速览
- 阶段
- 不适用
- 状态
- 撤回
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
- •Based on cut-off scores and in line with previous studies, we will include 20 patients with a PTSD (minimum severity score of 50 on the the Clinician-Administered PTSD Scale, CAPS-1; Blake et al., 1995). All patients will receive intensive exposure therapy as part of their standard clinical treatment at the Centre of Anxiety Disorder in Overwaal. If patients reveal a suboptimal outcome and still have a minimum severity score of 50* as measured by clinician rated and self-rating lists- they will be offered to participate in the rTMS trial if they are eligible. Their standard treatment will be continued but monitored.
排除标准
- •With regard to transcranial brain stimulation
- •* Epilepsy, convulsion or seizure (TMS)
- •* Serious head trauma or brain surgery
- •* Large or ferromagnetic metal parts in the head (except for a dental wire)
- •* Implanted cardiac pacemaker or neurostimulator
- •* Pregnancy;With regard to general experimental requirements
- •* History or current presence of any neurologic or psychiatric disease other than PTSD and its affective comorbid disorders (including personality disorders)
研究者
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