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

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Qué se está recopilando

Colección de datos

Quiénes están siendo reclutados

Enfermedades del Sistema Nervioso Central+9

+ Enfermedad

+ Enfermedades de los Ganglios Basales

De 18 a 65 años
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Cómo está diseñado el estudio

Observacional
Inicio del estudio: abril de 2004
Ver detalles del protocolo

Resumen

Patrocinador PrincipalNational Institute of Neurological Disorders and Stroke (NINDS)
Última actualización: 18 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 8 de abril de 2004

Fecha en la que se inscribió al primer participante.

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.

Título OficialTiming of Voluntary Movement in Patients With Tourette Syndrome and Chronic Tic Disorder Using EEG and Surface EMG 
NCT00081419
Patrocinador PrincipalNational Institute of Neurological Disorders and Stroke (NINDS)
Última actualización: 18 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 42 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

De 18 a 65 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Enfermedades del Sistema Nervioso CentralEnfermedadEnfermedades de los Ganglios BasalesEnfermedades del CerebroTrastornos MentalesSíndrome de TouretteTrastornos del MovimientoEnfermedades del sistema nerviosoManifestaciones NeurológicasProcesos PatológicosSíndromeTrastornos de Tic

Criterios

* 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

Centros del Estudio

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Este estudio tiene una ubicación

Suspendido

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, United StatesVer ubicación
Completado1 Centros de Estudio