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临床试验/NCT06600217
NCT06600217尚未招募不适用

Développement De La Stimulation Non-invasive En Boucle Fermée

University Hospital, Grenoble0 个研究点目标入组 60 人开始时间: 2024年10月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
主要终点
Quality of EEG markers extracted in real-time

研究概览

简要总结

Transcranial magnetic stimulation (TMS) is a widely used tool for exploring brain function in humans (Siebner et al. et al., 2022), which has led to new therapeutics for various psychiatric and neurological disorders (Lefaucheur et al., 2020). However, the open-loop use of this technique has raised questions about its operating principle, due to the high degree of heterogeneity of results and the small to medium observed effect sizes (Zrenner and Ziemann, 2023). To increase the response rate, it has been suggested to individualize stimulation, by adapting the TMS parameters (i.e. delivered dose, target dose, targeting, timing, etc.) to instantaneous estimates of brain brain state. Such an approach, known as closed-loop closed-loop stimulation, is currently one of the main challenges challenges in this field (closed-loop brain state-dependent stimulation). To this end, we are focusing on the combination of robotic TMS and electroencephalography (EEG) (Hernandez-Pavon et al. al., 2023). The closed-loop stimulations using this combination developed to date have two limitations: (i) they are not adaptive and focus focus mainly on calculating the phase of brain oscillations to trigger stimulation and (ii) are limited to central cortical (sensorimotor) areas, where the EEG signal-to-noise ratio is optimal.

This project aims to develop closed-loop TMS-EEG protocols that overcome these two limitations: (i) by incorporating adaptive decision modeling (AutoHS model, Harquel et al. 2017) to optimize several parameters in parallel (coil location, orientation, intensity) while using a wider range of EEG markers (evoked potentials, oscillatory activity strength, connectivity, etc.), and (ii) by integrating real-time EEG pre-processing to access any cortical target (including frontal, temporal and occipital lobes).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Signed informed consent
  • Having undergone a medical examination prior to participation in research
  • Affiliation with or beneficiary of a social security scheme

排除标准

  • Contraindications (CI) to MRI, EEG, TMS practice
  • Existence of a severe general medical condition: cardiac, respiratory, hematological, renal, hepatic, cancerous,
  • Regular use of anxiolytics, sedatives, antidepressants, neuroleptics,
  • Characterized psychiatric pathology,
  • Suspicion of alcohol ingestion prior to the examination,
  • Participation in other interventional research protocols in progress with exclusion period or in the preceding week.
  • Persons covered by articles L1121-5 to L1121-8 of the CSP (French Public Health Code) (corresponds to all protected persons: pregnant women, parturients, nursing mothers, persons deprived of their liberty by judicial or administrative decision, persons under psychiatric care under articles L.
  • 3212-1 and L. 3213-1 who are not covered by the provisions of article L. 1121-8, persons admitted to a health or social establishment for purposes other than research, minors, persons under legal protection or unable to express their consent).
  • Personnel with a hierarchical link to the principal investigator

结局指标

主要结局

Quality of EEG markers extracted in real-time

时间窗: During the two TMS-EEG experimental sessions, at day 0 and up to day 30

Quality of EEG markers extracted in real-time (evoked potentials, power and phase of brain oscillations and functional connectivity)

Quality of EEG marker modulation

时间窗: During the two TMS-EEG experimental sessions, at day 0 and up to day 30

Quality of EEG marker modulation induced by TMS parameters selected by the AutoHS decision model

次要结局

  • Intra-individual (inter-session) reproducibility of primary endpoint quality markers(Contrast between the 2 TMS-EEG experimental sessions, at day 0 up to day 30)

研究者

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

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