Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT05150106

Characterization of Clinical Phenotypes of Laryngeal Dystonia and Voice Tremor

Led by Massachusetts Eye and Ear Infirmary · Updated on 2025-12-02

165

Participants Needed

1

Research Sites

251 weeks

Total Duration

On this page

Sponsors

M

Massachusetts Eye and Ear Infirmary

Lead Sponsor

U

University of Utah

Collaborating Sponsor

AI-Summary

What this Trial Is About

The researchers will systematically evaluate current and novel clinical voice assessment tools and measures to elucidate distinct clinical phenotypes of those with laryngeal dystonia and voice tremor.

CONDITIONS

Official Title

Characterization of Clinical Phenotypes of Laryngeal Dystonia and Voice Tremor

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Males and females of diverse racial and ethnic backgrounds
  • Age 18-80 years
  • Native English speakers
  • Right-handed
  • Normal cognitive status
  • Patients with laryngeal dystonia or voice tremor
  • Healthy controls without neurological, psychiatric, or otolaryngological problems
Not Eligible

You will not qualify if you...

  • Unable to give informed consent
  • Pregnant or breastfeeding women until no longer pregnant or breastfeeding
  • Positive pregnancy test before MRI for women of childbearing potential
  • History of neurological problems such as stroke, brain tumors, movement disorders (except specified LD and VT), traumatic brain injury with loss of consciousness, ataxias, myopathies, myasthenia gravis, demyelinating diseases
  • History of psychiatric disorders including schizophrenia, bipolar depression, obsessive-compulsive disorder, alcoholism, drug dependence
  • Laryngeal problems like vocal fold paralysis, paresis, nodules, polyps, carcinoma, chronic laryngitis
  • Other forms of dystonia
  • Dystonia symptoms at rest or mirror dystonia
  • Patients not symptomatic due to recent botulinum toxin treatment (must be at least 3 months post-injection and fully symptomatic)
  • Use of medications affecting the central nervous system
  • History of head or neck surgery affecting regional anatomy or innervation
  • Presence of tattoos or ferromagnetic objects incompatible with MRI (e.g., implanted stimulators, surgical clips, prosthesis, artificial heart valve)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Massachusetts Eye and Ear and University of Utah

Boston, Massachusetts, United States, 02114

Actively Recruiting

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Research Team

K

Kristina Simonyan, MD, PhD

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

3

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