Actively Recruiting

Age: 18Years - 110Years
All Genders
ID05041387

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

Age: 18Years - 110Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • No other exclusion criteria for patients

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

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

Long-term Monitoring

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

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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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