Terminé

Neural Correlates of Observational Motor Learning in Chronic Stroke Patients

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Ce qui est collecté

Collecte de données

Qui peut participer

Maladies du cerveau+4

+ Maladies Cardiovasculaires

+ Maladies du système nerveux central

De 18 à 75 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Observationnel
Date de début : mai 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 : 25 mai 2004

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

In normal subjects, the learning of new hand movements initially relies on the automatic ability to elaborate a motor plan from the simple observation of movements performed by others. The improvement of motor performance during practice also relies on a correct visuomotor processing of visual feedback and it has been demonstrated that the repeated observation of a gesture, named observational training is sufficient to induce motor learning. However, it is not known if stroke patients process visuomotor information in the same manner as normal subjects. Objectives: The purpose of this protocol is to determine the pattern of brain activations related to motor learning induced by observational training in stroke patients as compared to normal volunteers. We hypothesize that observational motor learning in stroke patients will rely on an increased activity in premotor cortex as compared to normal volunteers. Study population: This protocol will include chronic stroke patients with subcortical lesions and good motor recovery from an initial upper-limb paresis, and a control population of age and gender matched normal volunteers. Design: We will conduct a functional MRI (fMRI) experiment assessing observational training of finger sequences. Three conditions of finger sequences will be compared: 1) a sequence visually trained during the fMRI session, 2) a non-trained sequence (control 1), and 3) a sequence visually trained before the fMRI session (control 2). The fMRI session will be split into 3 separate runs. The first run will assess brain activity related to the motor performance of the 3 finger sequences. The second run will explore the brain activity during observational training of the sequence. The third run will re-assess the brain activity related to the motor performance of the 3 finger sequences. Outcome measures: The endpoint measure of the experiment will be an increase in the number of activated voxels in premotor cortex during the motor learning induced by observational training in the stroke patients as compared to normal volunteers.

Titre officielNeural Correlates of Observational Motor Learning in Chronic Stroke Patients 
NCT00083642
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

60 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 75 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains non autorisés

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

Conditions

Pathologie

Maladies du cerveauMaladies CardiovasculairesMaladies du système nerveux centralTroubles cérébro-vasculairesMaladies du système nerveuxMaladies vasculairesAccident Vasculaire Cérébral

Critères

* INCLUSION CRITERIA: We will include PATIENTS: 1. Who are aged 18 to 75, 2. With a single thromboembolic non-hemorrhagic hemispheric lesions, 3. With at least a 3 months period since the stroke, 4. Who initially had a severe motor paresis (below MRC grade 2), 5. Who subsequently recovered to the point that they can perform the motor tasks of this study, 6. With no history of other neurological and psychiatric illness, 7. Who are right-handed (before the stroke history). As a control group, we will include NORMAL VOLUNTEERS, 1. Who are age- and gender matched to stroke PATIENTS, 2. Who can perform the motor tasks of this study, 3. With no history of other neurological and psychiatric illness, 4. Who are right-handed. EXCLUSION CRITERIA: 1. PATIENTS with more than one stroke in the medial cerebral artery territory. 2. PATIENTS with bilateral motor impairment. 3. PATIENTS with cerebellar or brainstem lesions. 4. PATIENTS and NORMAL VOLUNTEERS unable to perform the task. 5. PATIENTS and NORMAL VOLUNTEERS with history of severe alcohol or drug abuse, psychiatric illness like severe depression, poor motivational capacity, or severe language disturbances, particularly of receptive nature or with serious cognitive deficits (defined as equivalent to a mini-mental state exam score of 23 or less). 6. PATIENTS and NORMAL VOLUNTEERS with severe uncontrolled medical problems (e.g. cardiovascular disease, severe rheumatoid arthritis, active joint deformity of arthritic origin, active cancer or renal disease, any kind of end-stage pulmonary or cardiovascular disease, or a deteriorated condition due to age, uncontrolled epilepsy or others). 7. PATIENTS and NORMAL VOLUNTEERS with increased intracranial pressure (as evaluated by clinical examination). 8. PATIENTS and NORMAL VOLUNTEERS with unstable cardiac arrhythmia. 9. PATIENTS and NORMAL VOLUNTEERS with h/o hyperthyroidism or individuals receiving drugs acting primarily on the central nervous system. 10. PATIENTS and NORMAL VOLUNTEERS with more than moderate to severe microangiopathy (as assessed by multiple peri-ventricular T2 hyperintensity on the pre-experimental anatomical MRI), polyneuropathy (as assessed by clinical examination), diabetes mellitus (medical record), or ischemic peripheral disease (as assessed by clinical examination). 11. PATIENTS and NORMAL VOLUNTEERS who are or who have been good skilled piano or string instruments players. 12. PATIENTS and NORMAL VOLUNTEERS who is on medication with the potential to influence nervous system function, who has a history of surgery with metallic implants or a known history of metallic particles in the eye, a cardiac pacemaker, intracardiac lines, neural stimulators, cochlear implants. 13. PATIENTS and NORMAL VOLUNTEERS who are pregnant. 14. PATIENTS and NORMAL VOLUNTEERS with significant visual loss/deficits. 15. PATIENTS and NORMAL VOLUNTEERS with MRI contraindications.

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