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临床试验/NCT04450186
NCT04450186已完成不适用

Study Pilot - Hybrid EEG/fMRI Neurofeedback in Depressed Patients

Rennes University Hospital2 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2020年8月10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
31
试验地点
2
主要终点
Cerebral activation in fMRI

研究概览

简要总结

Cognitive impairment is a common residual symptom after a depressive episode and expose patients to a risk of relapsing or therapeutic resistance.

Neurofeedback (using ElectroEncephaloGraphy - EEG or functional Magnetic Resonance Imaging - fMRI) allows patients to self-regulate their cerebral activity, which is supposedly provided through an intelligible and motivating feedback.

Recent results exhibited clinical improvement in depressed patients who underwent a fMRI neurofeedback protocol targeting the amygdala. Furthermore, prefrontal alpha activity was temporally correlated to variations of the BOLD signal in the amygdala. Simultaneous fMRI/EEG neurofeedback is hypothesized to potentialize its antidepressant effect.

Our objective will be to test this assumption by conducting a double-blind randomized trial, and to prove the superiority of bimodal fMRI/EEG neurofeedback over fMRI neurofeedback alone in depressed patients.

An original visual feedback will be provided and validated beforehand by a pilot study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18 to 65 years old
  • Signature of an informed consent after being given clear and loyal oral and written information

排除标准

  • Related to the volunteer
  • Prior experience of a neurofeedback task
  • Related to the MRI
  • Implanted cardiac pacemaker of defibrillator
  • Brain aneurysm clip
  • Cochlear implant
  • Ocular on encephalic metallic foreign body
  • Endoprothesis implanted for less than 4 weeks and ostheosynthesis device implanted for less than 6 weeks.
  • Claustrophobia
  • Other criteria
  • Unstable hemodynamic status
  • Acute respiratory failure
  • Alteration of general state or continuous monitoring requirement
  • Other psychiatric condition (DSM-5) such as schizophrenia, substance abuse…
  • Neurological condition or diagnosis of dementia in medical history
  • Undergoing treatment by benzodiazepines or anticonvulsants prescribed less than a month prior to inclusion
  • Undergoing treatment influencing the blood flow prescribed less than three weeks prior to inclusion
  • Protected person (adults legally protected (under judicial protection, guardianship or supervision), person deprived of their liberty, pregnant woman, lactating woman and minor)

研究组 & 干预措施

EEG/fMRI neurofeedback

Experimental

Healthy volunteers

干预措施: EEG/fMRI neurofeedback (Other)

结局指标

主要结局

Cerebral activation in fMRI

时间窗: day 1

Measurement by an enregistrement in fMRI

EEG power in alpha band

时间窗: day 1

Measurement by an enregistrement in EEG

次要结局

  • Technology prone behaviour(day 1)
  • Anxious personality traits(day 1)
  • Mindfulness skills(day 1)

研究者

发起方
Rennes University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (2)

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