Terminé

Timing of Voluntary Movement in Patients With Tourette Syndrome and Chronic Tic Disorder Using EEG and Surface EMG

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Ce qui est collecté

Collecte de données

Qui peut participer

Maladies des ganglions de la base+15

+ Troubles Mentaux

+ Maladies du cerveau

De 18 à 65 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Observationnel
Date de début : avril 2004
Voir le détail du protocole

Résumé

Sponsor principalNational Institute of Neurological Disorders and Stroke (NINDS)
Dernière mise à jour : 18 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Date de début de l'étude : 8 avril 2004

Date à laquelle le premier participant a commencé l'étude.

OBJECTIVES: The purpose of this study is to determine how the subjective sense of willing and initiating an action is altered in patients with Tourette Syndrome and Chronic Tic Disorder. Although many definitions of the disease include the characterization of tics as 'involuntary', some patients claim that these movements are voluntarily made, or are unable to decide if they are voluntary or involuntary. Recent studies have shown that the time order in which someone wills a voluntary movement and begins that movement is central to the subjective sense of causality. We propose to examine tics as well as normal, voluntary movements in patients with Tourette Syndrome and Chronic Tic Disorder to identify the time course between the decision to move and the onset of movement. Using Libet's paradigm, we intend to have subjects watch a fast-rotating clock to report the times associated with willing (time W) and initiating (time M) movement; we will also determine electroencephalographic/electromyographic (EEG/EMG) measures of movement. STUDY POPULATION: We intend to study adult patients with a Diagnostic and Statistical Manual of Mental Disorders diagnosis of a tic disorder and frequent tics as well as normal, healthy volunteers as controls. DESIGN: We will ask tic patients to rate the "voluntariness" of their tics using a rating scale. We will ask tics patients to look at a fast-rotating clock on a computer screen and note when their movements were willed (time W) and were initiated (time M), for tics as well as normal voluntary movements. Patients will also report the time of a somatosensory stimulus. Surface EMG will determine the time of actual movement, and EEG will record brain potentials associated with movement. The design will be the same for the normal volunteers with the exception that the volunteers will not complete rating scales and will not be experiencing tics. OUTCOME MEASURES: The primary outcome measure of this study is the latency of times W and M (before EMG onset) in tics patients as correlated with the voluntariness the patients associate with their tics, compared to the time W and M reported for normal voluntary movements in the normal volunteers.

Titre officielTiming of Voluntary Movement in Patients With Tourette Syndrome and Chronic Tic Disorder Using EEG and Surface EMG 
NCT00081419
Sponsor principalNational Institute of Neurological Disorders and Stroke (NINDS)
Dernière mise à jour : 18 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

42 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

De 18 à 65 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Maladies des ganglions de la baseTroubles MentauxMaladies du cerveauMaladies du système nerveux centralMaladieSyndrome de TouretteTroubles du mouvementMaladies du système nerveuxManifestations NeurologiquesProcessus pathologiquesSyndromeTroubles TicsMaladies neurodégénérativesTroubles hérédo-dégénératifs du système nerveuxTicsDyskinésiesMaladies Génétiques CongénitalesTroubles du développement neurologique

Critères

* INCLUSION CRITERIA: Tic Patients: Patients will be men or women, ages 18-65, with a DSM-IV-TR diagnosis of TS or CTD. Patients will be screened in the NINDS Movement Disorders Outpatient Clinic, and will have neurological and physical examinations. They will be asked to abstain from alcohol and any medications for 24 hours before the study. All subjects participating in the studies will have a valid Clinical Center Medical Record Number. Normal Volunteers: Twenty-six normal controls will be included; controls will be screened in the NINDS Movement Disorders Outpatient Clinic, and will have neurological and physical examinations. They will be asked to abstain from alcohol and any medications for 24 hours before the study. All subjects participating in the studies will have a valid Clinical Center Medical Record Number. EXCLUSION CRITERIA: Patients younger than 18 years old or older than 65 years old will be excluded from the study. Tic Patients: Patients with neurological disorders other than TS or CTD Patients with Attention deficit hyperactivity disorder (ADHD) Patients who are not able to abstain from alcohol or medication affecting the central nervous system for 24 hours before the study Patients not capable of giving an informed consent Normal Subjects: Patients with neurological disorders or ADHD Patients who are not able to abstain from alcohol or medication affecting the central nervous system for 24 hours before the study Patients not capable of giving an informed consent

Centres d'étude

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Cette étude comporte 1 site

Suspendu

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, United StatesVoir le site
Terminé1 Centres d'Étude