Actively Recruiting
Data Collection of Standard Care of Patients in the EMG Section for Neuromuscular Disorders
Led by National Institute of Neurological Disorders and Stroke (NINDS) · Updated on 2026-03-10
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting data from adults with neuromuscular disorders who are not currently enrolled in other NIH studies. This observational study aims to build a repository of information to help generate future research hypotheses and improve understanding of various neuromuscular conditions. It also supports training programs for clinical neurophysiology fellows and keeps medical staff updated on a wide range of neuromuscular diseases. Participants will visit the NIH EMG Lab for evaluation using standard neurophysiological tests such as electromyography (EMG), autonomic nervous system testing, and neuromuscular ultrasound as needed. Additional assessments may include nerve conduction studies, sweat function tests, heart rate and blood pressure monitoring, and breathing or body position changes. These procedures are part of standard care and diagnostic evaluation. Each participant will have one or two visits lasting less than four hours each. During visits, physical exams and various assessments will be performed to evaluate nerve and muscle function. Data from participants will be stored securely with unique identifiers for future research use. Participants may be contacted for follow-up visits, and the primary goal is to create a valuable information repository over a 10-year period.
CONDITIONS
Brief Title
Data Collection of Standard Care of Patients in the EMG Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient or legally authorized representative can give informed consent and signs consent form
- Male or female, age 18 years or older
- Possible neuromuscular or neurodegenerative disorder
You will not qualify if you...
- No other exclusion criteria for patients
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Occurs at enrollment and as clinically indicated
Participants undergo standard neurophysiological studies including EMG, autonomic nervous system testing, and neuromuscular ultrasound as needed for diagnostic and clinical status assessment.
1 or more visits depending on clinical needs
Duration - Up to 10 years
Participants are observed over time to create a repository of information to support future research and training programs.
Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
C
Candida C Silva
T
Tanya J Lehky, M.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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