Terminé

fMRI Study on Mechanism of Rhythm Perception and Generation

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Ce qui est collecté

Collecte de données

Qui peut participer

De 21 à 65 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

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

Résumé

Sponsor principalNational Institute of Neurological Disorders and Stroke (NINDS)
Dernière mise à jour : 14 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Date de début de l'étude : 22 mars 2004

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

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.

Titre officielfMRI Study on Mechanism of Rhythm Perception and Generation 
NCT00080067
Sponsor principalNational Institute of Neurological Disorders and Stroke (NINDS)
Dernière mise à jour : 14 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

50 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.
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

De 21 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.

Critères

* 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

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