Noninvasive Brain Stimulation for Cervical Dystonia (NetworkStim)
The Effect of Noninvasive Brain Stimulation on Symptoms of Cervical Dystonia
The primary aim of this study is to assess whether continuous theta-burst stimulation (cTBS) can be helpful in reducing symptoms of idiopathic cervical dystonia. This will be a parallel-group, randomised, sham-controlled, double blind clinical trial. Patients and investigators measuring patient symptoms clinical scales will be blinded from allocation group, investigators delivering the intervention will not be blinded, as this is not feasible. Real cTBS will be compared to sham cTBS, with patients allocated to these two groups with a 1:1 recruitment ratio.
Bilateral cTBS will be delivered four times daily, over eight days, for a total of 32 bilateral cTBS sessions. The primary outcome is the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS). This will be administered at T1 (pre-cTBS), T2 (day 10, following days 2-9 where patients received the intervention), T3 (2 weeks post the final session of cTBS), and T4 (4-5 weeks post the final session of cTBS).
Secondary outcomes will be the TWSTRS subscales (severity, disability, pain), Quality of Life scale, Global dystonia severity rating scale (GDS), Fahn Tolosa Marin (FTM) modified (to include only questions relevant to head/neck tremor) tremor scale, kinematic data of patient's movement patterns, motor evoked potentials (MEPs), and resting-state fMRI data (fMRI).
研究概览
地位
条件
详细说明
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Daniel T Corp, PhD
- 电话号码:+393445660971
- 邮箱:danieltcorp@gmail.com
研究联系人备份
- 姓名:Ambra Salvati
- 电话号码:+393491028595
- 邮箱:ambra.salvati@unicampus.it
学习地点
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Roma
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Roma、Roma、意大利、00128
- 招聘中
- Università Campus Bio-Medico
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接触:
- Vincenzo Di Lazzaro, MD
- 电话号码:+39 06225411220
- 邮箱:v.dilazzaro@policlinicocampus.it
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接触:
- Ambra Salvati, Psy.D.
- 电话号码:+39 3491028595
- 邮箱:ambra.salvati@unicampus.it
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副研究员:
- Daniel T Corp, PhD
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria
- Aged between 18 and 85 years
- Diagnosis of idiopathic cervical dystonia made by an expert physician
- Last botulinum toxin injection administered at least two months before the start of participation in the study (Albanese, Abbruzzese et al. 2015)
Exclusion Criteria
- Head or neck trauma occurring less than 12 months before the onset of dystonia
- Acquired dystonia (e.g., drug-induced, brain lesions or trauma)
- History of major psychiatric disorders (e.g., bipolar disorder, schizophrenia, obsessive-compulsive disorder)
- History of neurological diseases other than CD (e.g., epilepsy, Parkinson's disease)
- Other contraindications for TMS or brain MRI (e.g., metal in the head)
- Pregnant or breastfeeding women
- History of substance abuse or dependence
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Active cTBS
The patients of this group will receive 4 sessions of bilateral somatosensory cortex cTBS per day for 8 days
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Continuous theta-burst stimulation (cTBS) will be delivered using a Magstim Rapid machine connected to a 70mm cooled coil at 80% of a participants resting motor threshold (RMT).
cTBS will consist of three-pulse bursts at 50Hz repeated every 200ms (5Hz) for 40 seconds (600 pulses total) (Huang, Edwards et al. 2005).
All cTBS procedures will be conducted bilaterally, with application first over the left hemisphere, before moving to the right (approximately one minute will separate each hemisphere).
Bilateral cTBS will be delivered four times daily, over eight days, for a total of 32 bilateral cTBS sessions.
This 4x day protocol will follow prior studies in neglect patients, delivered at time intervals of 0, 15, 60, and 75 minutes (Nyffeler, Cazzoli et al. 2008, Cazzoli, Müri et al. 2012, Nyffeler, Vanbellingen et al. 2019).
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假比较器:Sham cTBS
The patients of this group will receive 4 sessions of bilateral somatosensory cortex cTBS per day for 8 days, delivered using a sham TMS coil.
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Sham cTBS procedures will be identical to those in the active cTBS arm but applied using a 70mm sham TMS coil.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Symptoms of cervical dystonia - Toronto Western Spasmodic Torticollis Rating Scale total score
大体时间:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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The total score on the Toronto Western Spasmodic Torticollis Rating Scale.
Range: 0-85.
Higher scores mean worse symptoms.
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Motor evoked potentials
大体时间:For a single patient, 10 days. Pre and post cTBS
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Motor evoked potential amplitudes from input-output curves, measured using surface electromyography
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For a single patient, 10 days. Pre and post cTBS
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Magnetic resonance imaging
大体时间:For a single patient, 10 days. Pre and post cTBS
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Functional connectivity changes from pre-defined regions of interest in the brain
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For a single patient, 10 days. Pre and post cTBS
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Symptoms of cervical dystonia - Toronto Western Spasmodic Torticollis Rating Scale subscales
大体时间:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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The scores on each of the subscales of the Toronto Western Spasmodic Torticollis Rating Scale (severity, disability, pain).
Higher scores mean worse symptoms.
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Symptoms of cervical dystonia - kinematic recordings
大体时间:For a single patient, 10 days. Pre and post cTBS
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Metrics of patients' head and neck movements from a wearable motion sensor.
Higher scores will mean greater movement error.
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For a single patient, 10 days. Pre and post cTBS
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Fahn Tolosa Marin tremor scale
大体时间:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Measurement of head and neck tremor.
Higher scores mean worse symptoms.
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Global dystonia severity rating scale
大体时间:For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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Measurement of dystonia in all body parts.
Range: 0-100.
Higher scores mean worse symptoms.
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For a single patient, a minimum of 6 weeks and a maximum of 16 weeks
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合作者和调查者
调查人员
- 首席研究员:Vincenzo Di Lazzaro, MD、Campus Bio-Medico Hospital
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- NetworkStim 270.25 CET2 cbm
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 树液
- 国际碳纤维联合会
- 分析代码
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