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临床试验/NCT03964545
NCT03964545已完成不适用

Proof-of-concept and Validity of Amygdala-neurofeedback in Adolescent Patients With Emotion Dysregulation

Central Institute of Mental Health, Mannheim1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2018年5月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
28
试验地点
1
主要终点
Amygdala self-regulation

研究概览

简要总结

A treatment to improve emotion regulation is tested in young patients with trauma-related mental disorder. The Electrical FingerPrint (EFP) from the amygdala is used for presenting patients with feedback (i.e. neurofeedback) from the amygdala, a brain region which plays a critical role in emotion and mental disorder. Via feedback, patients learn to self-regulate the neural circuit of emotion.

详细描述

The study tests a neurofeedback treatment for emotion regulation training in adolescent patients suffering from emotional disturbances, indicated by diagnosis with borderline personality disorder (BPD) and/or post-traumatic stress disorder (PTSD), using innovative Electric Finger-Print (EFP) technology. With neurofeedback, patients can learn to regulate brain activation from emotion brain circuit. The technique allows neurofeedback training of sub-cortical brain activation outside the brain scanner, using an electroencephalography (EEG) surrogate of amygdala activation. The novel approach combines the advantages of functional magnetic resonance imaging (fMRI, i.e. high spatial resolution) and EEG (high scalability). EFP allows the probing of deep brain signals with scalp-electrodes, thus bridging a technological gap in neurofeedback training. The developers used EEG feature extraction and machine learning to receive model coefficients (i.e. the EFP) predicting amygdala BOLD activation based on EEG-channel activity (see Citations in this registration).

Participation in this trial is offered to patients who receive residential treatment at the adolescence center of the Central Institute of Mental Health (Mannheim, Germany) to obtain proof-of-concept in this special population, and to show potential value of adjuvant neurofeedback treatment. Patients in the treatment group receive 10 neurofeedback sessions within 5 weeks. Transfer is assessed with neural and questionnaire measures afterwards. A treatment-as-usual (TAU) control group does not receive the neurofeedback. We expect to replicate correlation of EFP with the blood oxygenation level dependent (BOLD) signal from the amygdala, which is tested via simultaneous fMRI-EEG data acquisition post-treatment. Additionally, we assume improved amygdala-BOLD regulation in an fMRI neurofeedback test.

This study aims to extend proof-of-concept of EFP neurofeedback to an adolescent population suffering from severe emotional disturbances.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Female patients will be included with four or more BPD and/or PTSD criteria (DSM-5)
  • •Willingness to participate in the study
  • •On residential treatment at adolescence center (Central Institute of Mental Health) throughout the study, including assessment of transfer.

排除标准

  • •General Pharmacological therapy with benzodiazepines
  • •Substance use
  • •Pregnancy
  • •Eplilepsy, traumatic brain injury, brain tumor or otherwise severe neurological or medical history
  • •BMI > 16.5
  • •Non-removable electrical implants
  • •Non-removable ferrous metal implants Permanent make-up and tattoos
  • •Claustrophobia

研究组 & 干预措施

EFP neurofeedback

Experimental

Ten sessions of EFP neurofeedback training. EEG is picked up with scalp electrodes, processed in real-time and returned to patients. One session lasts 30 min.

干预措施: neurofeedback (Behavioral)

Treatment as usual

No Intervention

Like patients from the treatment arm, these patients are on current residential treatment.

结局指标

主要结局

Amygdala self-regulation

时间窗: Change from baseline to 5 weeks

Amygdala BOLD regulation is assessed in a transfer task. Transfer task: Two 60s-blocks of BOLD fMRI neurofeedback (visual thermometer) with instruction to down-regulate.

次要结局

  • Alexithymia(Change from baseline to 5 weeks)

研究者

发起方
Central Institute of Mental Health, Mannheim
申办方类型
Other
责任方
Principal Investigator
主要研究者

Christian Paret

Principal Investigator

Central Institute of Mental Health, Mannheim

研究点 (1)

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