RECRUITING

An Observational Study of Individuals With Isolated Dystonia

Description

This is an observational study in individuals with isolated (or primary) dystonia that involves more than one body region. The purpose of the study is to collect detailed information to help your physician and other researchers understand how dystonia impacts your and other patients' lives and how the disease changes over time. The study may also help researchers better understand the clinical scales that are commonly used to evaluate dystonia symptoms and how they affect various areas of life such as well-being, pain, relationships and social interactions, and progress over time. Because this is an observational study, you will not receive any interventional treatment in the study.

Conditions

Isolated/Primary Dystonia That Affects More Than One Region of the Body
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Related Conditions:

Isolated/Primary Dystonia That Affects More Than One Region of the Body

Study Overview

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Study Details

Study overview

This is an observational study in individuals with isolated (or primary) dystonia that involves more than one body region. The purpose of the study is to collect detailed information to help your physician and other researchers understand how dystonia impacts your and other patients' lives and how the disease changes over time. The study may also help researchers better understand the clinical scales that are commonly used to evaluate dystonia symptoms and how they affect various areas of life such as well-being, pain, relationships and social interactions, and progress over time. Because this is an observational study, you will not receive any interventional treatment in the study.

An Observational Study of Individuals With Isolated Dystonia

An Observational Study of Individuals With Isolated Dystonia

Condition
Isolated/Primary Dystonia That Affects More Than One Region of the Body
Intervention / Treatment

-

Contacts and Locations

Scottsdale

Vima Site #004, Scottsdale, Arizona, United States, 85258

Aliso Viejo

Vima Site #010, Aliso Viejo, California, United States, 92656

Palo Alto

Vima Site #022, Palo Alto, California, United States, 94301

Englewood

Vima Site #019, Englewood, Colorado, United States, 80113

Boca Raton

Vima Site #003, Boca Raton, Florida, United States, 33486

Gainesville

Vima Site #009, Gainesville, Florida, United States, 32611

Miami

Vima Site #008, Miami, Florida, United States, 33176

Atlanta

Vima Site #005, Atlanta, Georgia, United States, 30322

Olney

Vima Site #007, Olney, Maryland, United States, 20832

Farmington Hills

Vima Site #002, Farmington Hills, Michigan, United States, 48334

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * The participant is willing to sign an informed consent form indicating that he/she understands the purpose of the study; understands and can perform, complete, and comply with all the assessments that are required during the study; and is willing to participate in the study.
  • * The participant is a male or female between 12 and 65 years of age (inclusive).
  • * The participant has a clinical diagnosis of isolated (or primary) dystonia for at least one year prior to Visit 1 and meets the study definition of segmental/multifocal or generalized dystonia at Visit 1.
  • * The participant has a diagnosis of focal dystonia at Visit 1.
  • * The participant has a diagnosis of dopa-responsive dystonia, secondary dystonia, or psychogenic/functional dystonia.
  • * The participant has any significant ongoing disease, disorder, laboratory abnormalities, alcohol or illicit drug abuse or dependence, environmental factor, or any ongoing or history of any medical or surgical condition that in the judgment of the investigator, in consultation with the medical monitor and/or sponsor's designee, might jeopardize the participant's safety, impact the scientific objectives of the clinical study, or interfere with participation in the clinical study.
  • * The participant has a history of any psychiatric or cognitive impairment disorder that, in the opinion of the investigator, may interfere with study conduct.
  • * The participant has had myotomy or denervation surgery in any affected muscles (e.g., peripheral denervation and/or spinal cord stimulation).
  • * The participant has marked limitation on passive range of motion that suggests contractures or other structural abnormality (e.g., cervical contractures or cervical spine syndrome).
  • * The participant has undergone deep brain stimulation (DBS) surgery (even if implant deactivated).

Ages Eligible for Study

12 Years to 65 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Vima Therapeutics,

Study Record Dates

2026-02