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Tactile Learning in Stroke Patients

Implicit Tactile Learning in Chronic Stroke Enhanced by Non-Invasive Brain Stimulation of the Somatosensory Cortex

This study will determine if stimulation of the stroke-injured side of the brain combined with stimulation to the paralyzed hand can temporarily improve the sense of touch in stroke patients.

Healthy normal volunteers and people who have had a single stroke within 3 months of entering the study that affected one side of the brain may be eligible for this study. All participants must be between 18 and 90 years old and must be right-handed. Candidates are screened with a medical history, neurological examination and magnetic resonance imaging (MRI) of the brain if one has not been done within 1 year of entering the study.

Participants undergo the following tests and procedures during four 2-day sessions over about 6 weeks:

  • Peripheral high-frequency stimulation: Small loudspeakers are taped to the fingertips and simple tactile pulses are passed through the skin. Stimulation may be sham or real.
  • Transcranial direct current stimulation: Two small rubber electrodes are taped to the head - one above the eye and the other on the back of the head. A current is passed between the two electrodes. Stimulation may be sham or real.
  • MRI: The subject lies in the scanner, a metal cylinder surrounded by a magnetic field, for about 40 minutes, lying still for up to 40 minutes at a time. An electrical stimulation is applied to the fingers of the right and left hand in separate sessions. Earplugs are worn to muffle the loud noises during the scanning. Functional MRI measures blood flow changes in the brain during the performance of specific tasks.
  • Behavioral measurements:

    • Grating orientation task: The subject responds as quickly as possible to a touch stimulus to the finger by saying whether the direction of the stimulus is vertical or horizontal.
    • Haptic object recognition task: The subject is given five categories of unfamiliar objects in the shape of cubes. During the task, identical objects are hidden in a sack. With eyes closed, the subject is asked to identify and find the objects from the sack as quickly as possible.
    • Pegboard test: The subject is asked to place several pegs into a corresponding hole of a pegboard as soon as possible.
    • Tapping task: The subject is asked to tap a metal stick on a metal plate as quickly as possible for 1 minute.
  • Paired-pulse transcranial magnetic stimulation: This test measures changes in brain activity. A wire coil is held on the scalp and a brief electrical current is passed through the coil, creating a magnetic pulse that stimulates the brain. The subject hears a click and may fee a pulling sensation on the skin under the coil, and there may be a twitch in the muscles of the face, arm or leg. Subjects may be asked to tense certain muscles slightly or perform other simple actions.
  • Paired-pulse somatosensory evoked potential mapping: This test measures brain activity in another brain area. The subject is seated in a chair with eyes closed. One electrode is placed above the eye and two others are placed on the back of the head. A short electrical stimulus is applied to a nerve in the wrist and brain activity is recorded while the stimulus is applied.
  • Surface electromyography: This test measures the electrical activity of muscles. Electrodes are filed with a conductive gel and taped to the skin.
  • Visual analog and mood scale: Subjects complete questionnaires about their attention, fatigue and mood.

연구 개요

상태

완전한

정황

상세 설명

Chronic stroke is often accompanied by tactile impairments that contribute to long-term disability in activities of daily living. While new rehabilitative interventions recently became available in the motor domain by using transcranial direct current stimulation (tDCS), there is no generally accepted treatment for tactile impairments after chronic stroke. Previous studies in healthy volunteers demonstrated that tactile acuity and haptic skills can be improved by applying a passive learning protocol to the fingertip (peripheral high-frequency stimulation, pHFS). Based on these findings, the purpose of this protocol is to enhance the beneficial effect of pHFS on implicit tactile and haptic learning in chronic stroke patients by a combined application of pHFS with tDCS (pHFS+tDCS) applied to the somatosensory cortex of the affected hemisphere. This approach might identify novel strategies to enhance functional recovery after stroke and might provide deeper insight into mechanistic information on the neural substrates involved in these behavioral gains. Primary outcome measures will be performance in a tactile grating orientation discrimination task (GOT) and in a haptic object recognition task. In order to obtain descriptive preliminary information on the relation between sensory improvements and motor deficits in chronic stroke patients, secondary outcome measures will be fine motor tasks such as a tapping task and a pegboard test (PBT) that require manual dexterity, handeye coordination, steadiness, and perceptual motor skills. To identify the operating mechanisms underlying hypothesized performance improvements after pHFS+tDCS, we will use paired-pulse protocols to evaluate changes in cortical excitability as well as fMRI in a subset of patients to identify cortical map reorganization in primary (SI) and secondary (SII) somatosensory cortex as well as in primary motor cortex (MI). Healthy volunteers will be tested (a) since there are no data available on performance of the haptic task in healthy subjects, (b) to obtain descriptive information on the influence of our interventions on this task for hypothesis generation purposes in our future investigations, and (c) because sensorimotor performance in the non-paretic hand of stroke patients is often not normal and therefore a poor sole control for performance of the paretic hand. Studies in chronic stroke patients will help address the main experimental hypothesis.

연구 유형

관찰

등록

70

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

연구 대상 성별

모두

설명

  • INCLUSION CRITERIA:

We will include left- and right-handed stroke patients, aged 18-90 years, with thromboembolic or hemorrhagic hemispheric lesions at least 3 months after the stroke. We will choose patients who initially had a severe motor paresis (below MRC grade 2), and subsequently recovered to the point that they have a residual motor deficit but can perform the required tasks. Moreover, only chronic stroke patients with moderate tactile deficits (defined by absolute touch thresholds below 4 N using von Frey filaments) who are able to differentiate the alignment of a grating dome (either orthogonal or parallel to the index finger) of at least 5 mm grooves that is applied on the fingertip will be included in the protocol.

Assessment of the initial functional state will be taken either from patient reports or medical records. Right-handed healthy volunteers, aged 18-90 years, should be able to concentrate on the required tasks. Handedness will be assessed by the Edinburgh inventory scale as well as the hand dominance test (HDT). We will additionally perform a pregnancy test for women of child-bearing potential. All experimental sessions will be on outpatient basis.

EXCLUSION CRITERIA:

Chronic stroke patients will be not be eligible for the study if they:

  • are unable to perform the behavioral tasks,
  • have a sensory neglect,
  • have had more than one clinical stroke,
  • have both sides of the brain affected,
  • have had a stroke in the cerebellum or brainstem,
  • have a history of alcohol or drug abuse or severe language disturbances or serious cognitive deficits,
  • have uncontrolled medical problems, such as heart, lung or kidney disease, epilepsy or diabetes mellitus,
  • have severe tactile deficits (defined by Frey filaments exerting a force of 4 N to the distal pad of the finger on the paretic and non-paretic hand),
  • are pregnant,
  • have a cardiac pacemaker, intracardiac lines, implanted medication pumps, neural stimulators, metal in the cranium, with the exception of dental braces in the mouth.

Exclusion criteria for healthy volunteers:

Healthy volunteers will not be eligible for the study if they:

  • are unable to perform the tasks,
  • have a history of alcohol or drug abuse or severe language disturbances or serious cognitive deficits,
  • have uncontrolled medical problems, such as heart, lung or kidney disease, epilepsy or diabetes mellitus,
  • have severe tactile deficits (defined by Frey filaments exerting a force of 4 N to the distal pad of the finger),
  • are pregnant,
  • have a cardiac pacemaker, intracardiac lines, implanted medication pumps, neural stimulators, metal in the cranium except in the mouth, dental braces.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

공동 작업자 및 조사자

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간행물 및 유용한 링크

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연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2006년 1월 25일

기본 완료 (실제)

2009년 10월 7일

연구 등록 날짜

최초 제출

2006년 1월 29일

QC 기준을 충족하는 최초 제출

2006년 1월 28일

처음 게시됨 (추정)

2006년 1월 30일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 7월 2일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 6월 30일

마지막으로 확인됨

2009년 10월 7일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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