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临床试验/NCT07531238
NCT07531238尚未招募不适用

Transcranial Temporal Interference Stimulation (tTIS) To Modulate Essential Tremor: A Single-Center, Proof-of-Concept Study (TremorTIS (Pilot))

University Hospital, Geneva1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2026年5月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
6
试验地点
1
主要终点
Tremor amplitude

研究概览

简要总结

The goal of this proof-of-concept study is to examine the effects of a relatively new, non-invasive electrical current-based technique, transcranial temporal interference stimulation (tTIS), in patients with Essential Tremor (ET). TTIS is delivered via a Digitimer Ltd. stimulator, the "DS5 Isolated Bipolar Constant Current Stimulator." The method enables targeting deep cerebral structures to selectively modulate neurons. The structure of interest in the present study is the ventralis intermedius (VIM) of the thalamus, which plays a key role in tremor generation in people with essential tremor. Therefore, techniques targeting the VIM nucleus can potentially improve the tremor and the quality of life in the long term, as is the case with MRI-guided high-intensity focused ultrasound (MRgHIFU). Despite its efficiency, MRgHIFU can lead to side effects that could benefit from improved predictive modeling. In our proof-of-concept study, the investigators aim to examine whether tTIS of the VIM nucleus can alter tremor characteristics and, therefore, mimic the effects of MRgHIFU. This work would pave the way for future clinical trials to design prediction tools for MRgHIFU if the investigators can demonstrate the positive impact of tTIS.

详细描述

Essential tremor (ET) represents one of the most common movement disorders worldwide, with an estimated prevalence of 1 % across all ages, increasing with age. Despite being considered a benign disease, it can nevertheless lead to significant functional impairment. Several drugs, such as beta-blockers, can be used to alleviate the tremor, but they may not be enough to improve the quality of life, and they can cause significant side effects.

The etiology and pathophysiology of ET are not yet fully understood. One pathophysiological hypothesis for ET is a deficiency in cerebellar GABAergic transmission, leading to abnormal oscillatory activity that interferes with motor function. This abnormal oscillatory activity converges on the thalamus, specifically in the ventralis intermedius (VIM) nucleus. Various surgical or disruptive medical techniques can target this nucleus in case of a drug-resistant tremor or drug intolerance.

One such technique is MRI-guided, high-intensity focused ultrasound thalamotomy (MRgHIFU), which results in a long-lasting, significant reduction of tremor in most cases. Despite the MRgHIFU's millimetric precision, the VIM is not directly visible on peri-operative MRI scans. MRgHIFU thalamotomy can also lead to side effects, such as modifications of sensations (paresthesia), speech difficulties (dysarthria), imbalance (ataxia), or even motor deficits (hemiparesis). Therefore, more accurate tools are needed to predict the effects of MRgHIFU.

One promising technique that could help clinicians predict the effects of MRgHIFU is transcranial temporal interference stimulation. This non-invasive neuromodulation technique uses two pairs of scalp electrodes, which deliver two slightly different high-frequency currents (e.g., f1 = 2.00 kHz; f2 = 2.01 kHz). Frequencies in the kHz range are too high to induce an effect on neurons and nerves. Still, due to their difference Δf = f2-f1, they both interfere in the depth of the brain to create a so-called amplitude-modulated envelope with a beat frequency falling in the physiological range (e.g., Δf = 10 Hz). This allows neuromodulation of deep structures-the VIM in this study-and avoids stimulation of the cortical structures at the same time. The investigators will use the Digitimer Ltd. "DS5 Isolated Bipolar Constant Current Stimulator" to deliver tTIS.

The goal of the proposed proof-of-concept study is to examine the effects of tTIS on tremor modulation in essential tremor patients who are candidates for MRgHIFU thermoablation of the VIM, and to compare the impact of tTIS with the "true" effect of tremor reduction after MRgHIFU. The primary outcome will be the change in tremor amplitude (in mm), as measured by Inertial Measurement Units (IMUs) comprising an accelerometer, a gyroscope, and a magnetometer. The secondary outcomes will be other quantitative tremor parameters, such as the frequency, angular and linear acceleration, and power, as well as safety outcomes.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • (for both arms):
  • Informed Consent signed by the subject;
  • Age ≥ 18 years;
  • Diagnosis of Essential Tremor (ET) based on the proposed criteria by the Movement Disorders Society;
  • Candidate for MRgHIFU thalamotomy

排除标准

  • (for both arms):
  • Unable to provide informed consent;
  • Severe sensory or cognitive impairment or musculoskeletal dysfunction that prohibits understanding instructions or performing the experimental tasks.
  • Only for patients undergoing the tTIS protocol (experimental arm):
  • Severe neuropsychiatric (e.g., major depression, severe dementia, psychosis) or unstable systemic diseases (e.g., severe progressive and unstable cancer, life-threatening infectious disease);
  • Inability to follow or non-compliance with the procedures of the study;
  • Contraindications for non-invasive brain stimulation:
  • Electronic or ferromagnetic medical implants or devices
  • History of seizures

研究组 & 干预措施

Experimental arm: tTIS stimulation protocol

Experimental

In this arm, patients with essential tremor who are candidates for MRgHIFU will undergo the tTIS stimulation protocol before MRgHIFU. The tremor changes will be monitored using Inertial Measurement Units (IMUs) during the tTIS, as well as after tTIS and MRgHIFU.

干预措施: Transcranial temporal interference stimulation (Device)

Experimental arm: tTIS stimulation protocol

Experimental

In this arm, patients with essential tremor who are candidates for MRgHIFU will undergo the tTIS stimulation protocol before MRgHIFU. The tremor changes will be monitored using Inertial Measurement Units (IMUs) during the tTIS, as well as after tTIS and MRgHIFU.

干预措施: Tremor monitoring through Inertial Measurement Units (IMUs) (Other)

Control arm: Tremor Monitoring

Other

In this arm, essential tremor patients who are candidates for MRgHIFU will undergo only tremor monitoring using Inertial Measurement Units (IMUs) before and after MRgHIFU.

干预措施: Tremor monitoring through Inertial Measurement Units (IMUs) (Other)

结局指标

主要结局

Tremor amplitude

时间窗: From enrollment to day 1 (D1) after MRgHIFU

Tremor amplitude, measured in mm in the 3 axes, using an Inertial Measurement Unit (IMU) secured on the dorsum of both hands of the essential tremor patient.

次要结局

  • Tremor peak frequency(From enrollment to day 1 (D1) post-MRgHIFU)
  • Frequency Width Half Maximum (FWHM)(From enrollment to day 1 (D1) post-MRgHIFU)
  • Tremor Stability Index (TSI)(From enrollment to day 1 (D1) post-MRgHIFU)
  • Power of the tremor(From enrollment to day 1 (D1) post-MRgHIFU)
  • Half-Width Power (HWP)(From enrollment to day 1 (D1) post-MRgHIFU)
  • Linear acceleration of tremor(From enrollment to day 1 (D1) post-MRgHIFU)
  • Angular velocity of tremor(From enrollment to day 1 (D1) post-MRgHIFU)
  • Safety outcomes(From enrollment to day 1 (D1) post-stimulation)
  • Incidence of Device-Emergent (Serious) Adverse Events [Safety](From enrollment to day 1 (D1) post-stimulation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Vanessa Fleury

Head of the Movement Disorders unit, Neurology Department

University Hospital, Geneva

研究点 (1)

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