Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Enhancing Brain Activity With Magnetic Stimulation

Enhancing Interhemispheric Disinhibition Between Motor Cortices Using Bilateral Brain Stimulation

This study will determine whether stimulation of the right side of the brain with repetitive transcranial magnetic stimulation (rTMS) followed by stimulation of the left side with theta burst stimulation (TBS) can temporarily change brain activity and improve hand movements in subjects more than has recently been achieved with rTMS alone.

For rTMS, a wire coil is held on the patient's scalp. A brief electrical current is passed through the coil, creating a magnetic pulse that stimulates the brain. The subject hears a click and may feel a pulling sensation on the skin under the coil. There may be a twitch in the muscles of the face, arm or leg. The subject may be asked to tense certain muscles slightly or perform other simple actions. The effect of TMS on the muscles is detected with small metal disk electrodes taped to the skin of the arms or legs. This study uses two kinds of rTMS. In one (Hz rTMS), magnetic pulses are given once per second for a period of 20 minutes; in the other (TBS), a series of pulses are given in bursts, each lasting 2 seconds, for a period of 3 minutes.

Healthy normal volunteers between 18 and 55 years of age may be eligible for this study. Participants undergo the following procedures during three visits to the NIH Clinical Center:

Visit 1:

Participants receive either real or sham rTMS applied on the right side of the brain followed by real or sham TBS applied on the left side of the brain. In addition, subjects undergo the following:

" Pinch force: Subjects press a wedged instrument between the thumb and index finger as hard as they can during several trials every 10 seconds.

" Speed tapping: Subjects press a key on a computer keyboard as quickly as possible for 10 seconds, repeated for several trials.

" Simple reaction time: Subjects respond as quickly as possible to a "go" signal presented on a computer monitor by performing a quick wrist movement.

" Electromyography: Subjects' muscle activity is recorded using electrodes (small metal disks) filled with conductive gel and taped to the skin over the muscle.

Visits 2 and 3

Visit 2 is scheduled for one day after visit 1, and visit 3 is one week after visit 1. Participants do not have brain stimulation during these two visits, but they have TMS measurements, behavioral measurements, and electromyography (EMG) to see if the brain stimulation done during the first visit is still present after a period of time.

At all three visits, participants comp...

Panoramica dello studio

Stato

Completato

Condizioni

Descrizione dettagliata

OBJECTIVES:

Previous studies have demonstrated that single-pulse transcranial magnetic stimulation (TMS) applied to the primary motor cortex (MI) exerts a transient inhibitory effect on the contralateral MI. Furthermore, down-regulation of excitability in MI of one hemisphere by 1Hz rTMS results in increased excitability in the homologous MI accompanied by performance improvements in simple motor tasks performed by the hand ipsilateral to rTMS. It has been proposed that this phenomenon relies on interhemispheric disinhibition between both MI. Furthermore, interhemispheric disinhibition is also a promising method for boosting neurorehabilitation since interhemispheric disinhibition has been successfully applied in stroke patients to enhance motor cortex excitability and hand function or reduce aphasia. The purpose of this protocol is to test the hypothesis that interhemispheric disinhibition of the left MI by down-regulating activity in the right MI can be further enhanced by additional up-regulation targeting the left MI.

STUDY POPULATION:

We will study a total number of 72 healthy volunteers between the ages of 18-55.

DESIGN:

To test the hypothesis, subjects will be randomly allocated to one of 4 experimental sessions (parallel design). Subjects will receive different types of combined brain stimulation (1 Hz rTMS and Theta Burst Stimulation [TBS]) to the right and left MI. The primary outcome measure will be the amount of changes in cortical excitability, as reflected by recruitment curves (RC) of motor evoked potentials (MEPs) elicited by single-pulse TMS over the left MI. Additionally, we will test changes in short-interval intracortical inhibition (SICI) and facilitation (ICF) as well as the modulation of interhemispheric inhibition (IHI) between both MI. The secondary outcome measures will include simple motor tasks such as finger tapping, pinch force/acceleration and reaction time of the right hand.

In summary, we believe that this approach might identify additional effective strategies to enhance functional recovery after stroke and might provide deeper insight into the neural substrates involved in performance improvements after bilateral brain stimulation.

Tipo di studio

Osservativo

Iscrizione

72

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Maryland
      • Bethesda, Maryland, Stati Uniti, 20892
        • National Institutes of Health Clinical Center, 9000 Rockville Pike

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 55 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

  • INCLUSION CRITERIA:

    1. Age between 18-55 years
    2. Able to perform tasks required by the study
    3. Willing and able to give consent

EXCLUSION CRITERIA:

Subjects are not eligible for this experiment if they:

  1. Are unable to perform the tasks
  2. Have history of severe alcohol or drug abuse, psychiatric illness
  3. Have problems with movement of the hands
  4. Are currently under medication with central acting drugs
  5. Are left-handed
  6. Have uncontrolled medical problems, such as heart, lung or kidney disease, epilepsy, or diabetes mellitus
  7. Have a cardiac pacemaker, intracardiac lines, implanted medication pumps, neural stimulators, and metal in the cranium, with the exception of dental braces
  8. Are pregnant

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

3 novembre 2006

Completamento dello studio

15 dicembre 2008

Date di iscrizione allo studio

Primo inviato

7 novembre 2006

Primo inviato che soddisfa i criteri di controllo qualità

7 novembre 2006

Primo Inserito (Stima)

8 novembre 2006

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

2 luglio 2017

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 giugno 2017

Ultimo verificato

15 dicembre 2008

Maggiori informazioni

Termini relativi a questo studio

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

3
Sottoscrivi