MedPath

Physiological Investigations of Movement Disorders

Not Applicable
Completed
Conditions
Parkinson's Disease
Tic Disorders
Tourette's Syndrome
Dystonia
Movement Disorders
Interventions
Procedure: Transcranial Direct Current Stimulation (tDCS)
Device: Eye-tracking Device
Device: Pulsed vibrator
Other: Gait Trainer Treadmill (GTT)
Other: Standard psychiatric scales SCID-I, YBOCS and SCI-OBS-lifetime and cognitive scales MMSE and MOCA
Device: iMobility
Device: QMAT
Diagnostic Test: Treadmill Test
Device: Arm Intellistretch Device
Procedure: Transcranial Sonography (TCS)
Other: Behavioral tasks
Procedure: TMS single/paired pulse
Procedure: MEG
Procedure: EEG
Procedure: MRI techniques
Procedure: Peripheral Nerve Stimulation
Procedure: EMG
Procedure: Trancutaneous spinal direct current stimulation (tsDCS)
Registration Number
NCT01019343
Lead Sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
Brief Summary

Background:

* Previous studies have given researchers information on how the brain controls movement, how people learn to make fine, skilled movements, and why some people have movement disorders. However, further research is needed to learn more about the causes of most movement disorders, such as Parkinson's disease.

* By using small, specialized studies to evaluate people with movement disorders and compare them with healthy volunteers, researchers hope to learn more about the changes in the brain and possible causes of movement disorders.

Objectives:

* To better understand how the brain controls movement.

* To learn more about movement disorders.

* To train movement disorder specialists.

Eligibility:

* Individuals 18 years of age or older who have had a movement disorder diagnosed by a neurologist and are able to participate based on the specific requirements of the small study.

* Healthy volunteers 18 years of age or older.

Design:

* Participants will have a screening visit with medical history, physical examination, and questionnaire to determine eligibility. Eligible participants will give consent to participate in up to seven additional outpatient visits for study procedures. The number of sessions and the procedures needed for participation depend on specific symptoms.

* Participants must avoid drinking alcohol or caffeinated drinks (sodas, coffee, and tea) for at least 2 days (48 hours) before each session.

* Potential studies may include magnetic resonance imaging (MRI) scans, functional MRI scans, electroencephalography, magnetoencephalography, transcranial magnetic stimulation, nerve and sensory stimulation, or movement and mental tasks during any of the above procedures.

* This study does not provide treatment for movement disorders. Participants will not have to stop any treatment in order to participate.

Detailed Description

Objectives

The purpose of this protocol is to improve understanding of the pathophysiology of movement disorders by performing small behavioral, electrophysiological and neuroimaging sub-studies. This will allow identifying dysfunction of the central nervous system that causes behavioral abnormalities seen in movement disorder patients. This will also help to determine potential diagnostic or therapeutic targets. Some sub-studies will require healthy volunteers. We will conduct:

* Pilot Sub-study (previously labeled as Small Pilot Sub-studies) Pilot sub-studies are exploratory in nature, in order to develop enough information to generate a hypothesis. The criterion for transition to a new full protocol will be a sufficient amount of information to generate a power analysis. There are no enrollment limitations for pilot sub-studies.Small substudies to pilot investigations for larger studies,

* Hypothesis-Testing Sub-study (previously labeled small number sSub-studies) is defined as a study with a specific hypothesis to be thattested that can be completed with a few subjects healthy volunteers or patients, , Hypothesis-testing sub-studies will undergo statistical and PIRC review after 6 subjects (if there is one group) or after 12 (six per arm) if two groups are studied before additional subjects are recruited. Together, the P.I. and PIRC will decide whether to continue the hypothesis sub-study with more subjects or if a new protocol is necessary. A memo requesting a review of hypothesis-testing sub-studies for possible additional enrollment will be sent to PIRC and the statistical reviewer. If the action to request accrual increase proceeds beyond PIRC to the IRB, then it needs to be submitted in the form of an amendment for prospective review/approval.

* Individual patient investigations that may increase knowledge of a disease process or be helpful in patient diagnosis,

* Training for investigators who do not have prior experience using electrophysiological and neuroimaging techniques,

* Technical development of new experimental paradigms.

This protocol includes only non-invasive techniques with minimal risk (MRI, EEG, MEG, peripheral nerve stimulation, TMS).

Study population

We intend to study 1200 healthy volunteers and 1000 patients with diagnoses of movement disorders.

Design

We will design small projects as ideas arise in our patient population that are pertinent to the theme of movement disorder pathophysiology. We will investigate patients with movement disorders or healthy volunteers in the resting state or while they perform simple motor or sensory tasks. If a small study leads to results of interest and if a larger population is necessary to reach statistical significance, a separate protocol will be submitted with a priori hypotheses, specific study design and power analysis adapted from the pilot or exploratory sub-studies performed in the present protocol.

Outcome measures

MRI: we will analyze measures such as the amplitude of the BOLD signal (fMRI); tractography between seed and target regions of interest (using DTI); morphometry of brain regions (using VBM); and different neurotransmitter levels in brain regions of interest (using MRS).

EEG and MEG: we will quantify measures such as event- or task-related potentials, synchronization/desynchronization, and coherence between sensors or sources located close to the brain areas of interest.

TMS: we will analyze measures such as MEP amplitude and central conduction time.

Behavioral measures: we will quantify measures such as reaction times to initiate movements, EMG patterns, movement kinematics (position, velocity, acceleration, curvature).

We may measure autonomic data during the course of the experiment (such as blood pressure, skin conductance, and respiratory rate) which would correlate to the outcome measures.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1273
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Healthy VolunteersStandard psychiatric scales SCID-I, YBOCS and SCI-OBS-lifetime and cognitive scales MMSE and MOCAHealthy Volunteers
Healthy VolunteersArm Intellistretch DeviceHealthy Volunteers
Healthy VolunteersMEGHealthy Volunteers
Healthy VolunteersTranscranial Direct Current Stimulation (tDCS)Healthy Volunteers
Healthy VolunteersQMATHealthy Volunteers
Healthy VolunteersTranscranial Sonography (TCS)Healthy Volunteers
Healthy VolunteersTMS single/paired pulseHealthy Volunteers
Healthy VolunteersEEGHealthy Volunteers
Movement DisorderTranscranial Direct Current Stimulation (tDCS)Subjects diagnosed with movement disorder
Movement DisorderPulsed vibratorSubjects diagnosed with movement disorder
Movement DisorderGait Trainer Treadmill (GTT)Subjects diagnosed with movement disorder
Movement DisorderArm Intellistretch DeviceSubjects diagnosed with movement disorder
Healthy VolunteersEye-tracking DeviceHealthy Volunteers
Healthy VolunteersPulsed vibratorHealthy Volunteers
Healthy VolunteersiMobilityHealthy Volunteers
Healthy VolunteersTreadmill TestHealthy Volunteers
Healthy VolunteersBehavioral tasksHealthy Volunteers
Healthy VolunteersGait Trainer Treadmill (GTT)Healthy Volunteers
Healthy VolunteersMRI techniquesHealthy Volunteers
Movement DisorderTMS single/paired pulseSubjects diagnosed with movement disorder
Healthy VolunteersPeripheral Nerve StimulationHealthy Volunteers
Movement DisorderEye-tracking DeviceSubjects diagnosed with movement disorder
Movement DisorderiMobilitySubjects diagnosed with movement disorder
Movement DisorderQMATSubjects diagnosed with movement disorder
Movement DisorderTreadmill TestSubjects diagnosed with movement disorder
Movement DisorderMRI techniquesSubjects diagnosed with movement disorder
Healthy VolunteersEMGHealthy Volunteers
Movement DisorderMEGSubjects diagnosed with movement disorder
Movement DisorderPeripheral Nerve StimulationSubjects diagnosed with movement disorder
Movement DisorderTrancutaneous spinal direct current stimulation (tsDCS)Subjects diagnosed with movement disorder
Healthy VolunteersTrancutaneous spinal direct current stimulation (tsDCS)Healthy Volunteers
Movement DisorderStandard psychiatric scales SCID-I, YBOCS and SCI-OBS-lifetime and cognitive scales MMSE and MOCASubjects diagnosed with movement disorder
Movement DisorderTranscranial Sonography (TCS)Subjects diagnosed with movement disorder
Movement DisorderBehavioral tasksSubjects diagnosed with movement disorder
Movement DisorderEEGSubjects diagnosed with movement disorder
Movement DisorderEMGSubjects diagnosed with movement disorder
Primary Outcome Measures
NameTimeMethod
EEG and MEGthroughout

quantify measures such as event- or task-related potentials, synchronization/desynchronization, and coherence between sensors or sources located close to the brain areas of interest.

Behavioral measuresthroughout

quantify measures such as reaction times to initiate movements, EMG patterns, movement kinematics (position, velocity, acceleration, curvature), eye movement.

MRIthroughout

analyze measures such as the amplitude of the BOLD signal (fMRI); tractography between seed and target regions of interest (using DTI); morphometry of brain regions (using VBM); and different neurotransmitter levels in brain regions of interest (using MRS).

TMSthroughout

analyze measures such as MEP amplitude and central conduction time.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

National Institutes of Health Clinical Center

🇺🇸

Bethesda, Maryland, United States

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