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fMRI Study on Mechanism of Rhythm Perception and Generation

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Qué se está recopilando

Colección de datos

Quiénes están siendo reclutados

De 21 a 65 años
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Cómo está diseñado el estudio

Observacional
Inicio del estudio: marzo de 2004
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Resumen

Patrocinador PrincipalNational Institute of Neurological Disorders and Stroke (NINDS)
Última actualización: 14 de enero de 2026
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 22 de marzo de 2004

Fecha en la que se inscribió al primer participante.

Objective Rhythmic movements, such as finger tapping, are relatively simple. However, many brain areas including motor, somatosensory, premotor and prefrontal cortex, supplementary motor area, basal ganglia, cerebellum, etc. have been reported to be activated during rhythmic movements. Patients with lesions located in the extrapyramidal or cerebellar system, such as patients with Parkinson's disease, cerebellar ataxia or stroke with a lesion in these systems, have difficulties in performing rhythmic movements. Timing deficits after basal ganglia or cerebellar damage could also be due to abnormalities in interconnecting cortical systems commonly associated with these processes. Few studies have examined involvement of cerebral cortex in time perception. The purpose of this study is to detect the brain areas associated with three hypothesized processes associated with rhythm perception and generation: (1) perception of external rhythmic stimulation, (2) internal rhythm generation and (3) execution of rhythmic movement. To investigate whether the process of rhythm perception is common across sensory modalities, we will use auditory and visual stimulation. Study population This research will be conducted using normal adult volunteers. Design Using functional magnetic resonance imaging, we will examine the brain activity of subjects while they will hear or watch rhythmic stimulation and press buttons rhythmically with their fingers. A series of experiments will be designed to demonstrate the hypothesized three processes separately. Outcome measures The brain activity correlated with experimental conditions and behavioral data (the timing error of button press to the corresponding rhythmic stimulation) will be collected and analyzed by using statistical parametric mapping (SPM). The findings we expect to obtain with this experiment will contribute to basic knowledge for better understanding of the pathophysiology of the disturbance of perception and generation of rhythm in patients with neurological disorders, and give theoretical background for repetitive, rhythmically patterned movement training in neurorehabilitation.

Título OficialfMRI Study on Mechanism of Rhythm Perception and Generation 
NCT00080067
Patrocinador PrincipalNational Institute of Neurological Disorders and Stroke (NINDS)
Última actualización: 14 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 50 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.
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

De 21 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.

Criterios

* INCLUSION CRITERIA: Fifty healthy, right-handed adult (aged between 21 to 65 years old) volunteers will be recruited from people who are registered as HMCS normal volunteers. All subjects participating in MR studies should have a valid Clinical Center Medical Record Number. Female subjects of childbearing potential will have a pregnancy test and a specific interview prior to the study to ensure that pregnant subjects will not participate in the study. EXCLUSION CRITERIA: Subjects with implanted devices such as pacemakers, medication pumps or defibrillators, metal in the cranium except mouth, intracardiac lines, history of shrapnel injury or any other condition/device that may be contraindicated or prevent the acquisition of MRI. Pregnant female. A pregnancy test will be performed within 24 hours preceding each MRI and if the result is positive, that subject will not be studied. Subjects with claustrophobia Subjects with any visual, motor or hearing difficulties Musicians

Centros del Estudio

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Suspendido

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, United StatesVer ubicación
Completado1 Centros de Estudio