Actively Recruiting
TREMOR IN CHARCOT-MARIE-TOOTH
Led by University Medical Center Goettingen · Updated on 2026-05-06
75
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
TREMOR IN CHARCOT-MARIE-TOOTH
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of Charcot-Marie-Tooth disease or be part of a healthy control group
- Genetic confirmation of Charcot-Marie-Tooth disease in adult patients
- Ability to complete the baseline outcome measurements
- Age between 18 and 65 years
- Ability to provide informed consent and sign the consent form
You will not qualify if you...
- Pregnancy or breastfeeding
- Other significant neurological or psychiatric disorders, either current or past
- Presence of a serious previous internal disease
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Medical Centre
Göttingen, Lower Saxony, Germany, 37075
Actively Recruiting
Research Team
M
Michael W Sereda, Prof. MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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