Functional Connectivity of the Basal Ganglia in Primary Focal Dystonia

Primary Objective

Aim 1: A second level contrast between Primary Focal Dystonia (PFD) and Healthy Controls (HC) of the statistical parametric maps of correlation coefficients at rest and during a tapping motor task Aim 2: the strength of correlation between basal ganglia motor network functional connectivity measures and total PFD clinical assessment scale scores

This Study is
No Longer Enrolling

Description

In this study we are looking at how the brain works in people who have dystonia compared to those who don't have dystonia. This study will use magnetic resonance imaging (MRI), magnetoencephalography (MEG), and Electroencephalography (EEG) to see how the brain reacts while resting and doing a finger-tapping task.

Details
Age

Adult

Eligibility

Inclusion 1. All subjects must be over the age of 18. 2. Primary Focal Dystonia patients must have had their diagnosis made by a neurologist with subspecialty training in movement disorders. 3. Dystonia patients must be on a stable dose of all medications used to treat dystonia or neuroactive medications (e.g. antidepressants) for the prior month and not have been injected with botulinum toxin within the prior 2 months. Exclusion 1. Subjects will be excluded for: 2. (1) any contraindication to MRI scanning, 3. (2) any untreated neurological or psychiatric condition, 4. (3) evidence on neurological exam of any potentially confounding neurological disorder (e.g., Parkinson disease, Essential Tremor, etc.), 5. (4) evidence of significant cognitive impairment (all subjects assessed using the Montreal Cognitive Assessment and excluded if < 26).27,28 6. Patients with dystonia symptoms beginning prior to the age of 18 will be excluded as childhood onset dystonia typically represents a primary generalized form of dystonia. 7. Patients with secondary dystonia resulting from medications (e.g. anti-psychotics or metoclopramide) or that are part of another neurological disorder (e.g. Parkinson disease) will be excluded. 8. Patients with severe dystonic symptoms that could interfere with MRI scanning will be excluded

Phase

Not Applicable - Describes studies without FDA-defined phases, including studies of devices or behavioral interventions.

Type of Study

Observational

Scope

Local

Locations

Colorado Research Center
Department Specific Free Standing Clinic
University of Colorado Hospital

Study ID

Protocol Number: 12-0289

More information available at ClinicalTrials.gov: NCT01761903

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