TREMOR IN CHARCOT-MARIE-TOOTH (CMT-TREM)
Investigation of Tremor in Patients With Charcot-Marie-Tooth Neuropathy
Tremor is a symptom that has already been described in many case reports and case series concerning patients with Charcot-Marie-Tooth (CMT) disease. However, the pathophysiology of tremor in this condition remains largely unclear. It has also not been sufficiently investigated to what extent tremor in CMT patients constitutes a relevant impairment of quality of life.
This project focuses on a more detailed characterization of tremor in CMT patients using surface electromyography and accelerometer analysis, as well as the collection of individual clinical data, particularly regarding the symptom of tremor, in order to facilitate the characterization and etiological classification of the tremor. In addition, a questionnaire-based assessment will be conducted to capture the impact of tremor on activities of daily living and the associated burden in this specific patient cohort.
The entire data collection process will be supported by a clinical examination, which will be video-recorded by experienced neurologists to ensure more reliable analysis. This serves both the characterization of tremor and the illustration of its functional limitations. Where available, the data will be correlated with genetic variants to allow conclusions about possible genetic predispositions or disease progression. As a control group, CMT patients who have not yet reported a tremor will be included.
研究概览
地位
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Michael W Sereda, Prof. MD
- 电话号码:+49 551 3964162
- 邮箱:sereda@mpinat.mpg.de
学习地点
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Lower Saxony
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Göttingen、Lower Saxony、德国、37075
- 招聘中
- University Medical Centre
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接触:
- Sandrin Plewe
- 电话号码:+49 551 3964162
- 邮箱:sandrin.plewe@med.uni-goettingen.de
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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
取样方法
研究人群
描述
Inclusion Criteria:
- Clinical CMT Diagnosis / Anamnestically Healthy Control Group
- Genetic confirmation of CMT in adult patients
- Ability to achieve the outcome measure at baseline
- Age between 18 and 65 years
- Capacity of all study participants to consent and signed informed consent, including patient or participant information and consent form
Exclusion Criteria:
- Pregnancy or breastfeeding period
- Other relevant neurological or psychiatric disorders, acute or in the past history
- Presence of a serious previous internal disease
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
|---|
|
控件
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CMT患者
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Activities of Daily Living -Questionaire(ADL)
大体时间:baseline
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baseline
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Assessment of Handicap - Questionaire
大体时间:baseline
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baseline
|
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Fahn Tolosa Marin Rating Scale
大体时间:baseline
|
baseline
|
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Electrophysiological characterization of tremor using surface EMG and accelerometer analysis
大体时间:baseline
|
baseline
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
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MDS-UPDRS Part III without Tremor
大体时间:baseline
|
baseline
|
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SARA Score
大体时间:baseline
|
baseline
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合作者和调查者
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
关键字
其他相关的 MeSH 术语
其他研究编号
- 17/05/2024_C3
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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