- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01644929
Rehabilitation Combined With Bihemispherictranscranial Direct Current Stimulation in Subacute Ischemic Stroke (RECOMBINE)
Rehabilitation Combined With Bihemispherictranscranial Direct Current Stimulation in Subacute Ischemic Stroke to Increase Upper Limb Motor Recovery, a Randomised, Controlled, Double-blind Study
Rehabilitation after stroke improves motor functions by promoting plastic changes however, after completing standard rehabilitation, 50-60% of patients still exhibit some degree of motor impairment and require at least partial assistance in activities of day living. Therefore, the exploration of other approaches to promote recovery is compulsory. Non invasive brain stimulation and motor rehabilitation are thought to share similar mechanisms in inducing neuroplastic changes in the human cortex and an emerging field of research is focusing on the possibility of coupling both therapies in order to achieve an additive effect and improve outcome.
We hypothesize that coupling bihemispheric transcranial direct current stimulation (tDCS) with simultaneous physical/occupational therapy in the subacute phase of ischemic stroke patients may improve upper limb motor recovery in humans.
This is a randomized, controlled, double blind, cross-over, multicentre, clinical trial. Thirty-six ischemic stroke patients in the subacute phase will be recruited in three centers of neurorehabilitation in Switzerland. After stratification based on the Fugl-Meyer Assessment Upper Extremity according to the severity of the deficit, the patient will be randomized to receive besides standardized physical/occupational treatment according to the Impairment-Oriented Training, tDCS of themotor cortex (1.5 mA, 30 minutes) (group 1: 12 patients) or sham stimulation (without current) (group 2: 12 patients). After three weeks of treatment group 1 and 2 will cross-over and will be treated for other three weeks. Group 3 (12 patients) will receive routine physical/occupational treatment and sham tDCS for six weeks. Assessment will be performed before starting tDCS, at week 3, 6 and at 6 months. Outcome measures are the Fugl-Meyer Assessment Upper Extremity, the extended Barthel Index, the Ashworth scale, the Test of Upper Limb Apraxia (only baseline, week 6, month6), the grip strength evaluated by the Jamar Hydraulic Hand dynamometer. At baseline at week 6 and at month 6 depression will be assessed by the Hamilton depression Rating Scale.
연구 개요
상태
연구 유형
등록 (예상)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Bern, 스위스, 3010
- 빼는
- Universitätsspital Bern, Inselspital, Neuropsychologische Rehabilitation
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Brissago, 스위스, 6614
- 모병
- Clinica Hildebrand, Centro di riabilitazione Brissago
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연락하다:
- Paolo Rossi, MD
- 전화번호: +41 91 786 86 86
- 이메일: p.rossi@clinica-hildebrand.ch
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수석 연구원:
- Paolo Rossi, MD
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Zihlschlacht, 스위스, 8588
- 종료됨
- HELIOS Klinik Zihlschlacht AG, Neurologisches Rehabilitationszentrum
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Ischemic lesions in the territory of middle cerebral artery subcortical or subcortical/cortical confirmed neuroimaging
- Inclusion must be in the sub-acute phase defined as within 2-4 weeks after stroke
- Persistent hemiparesis, indicated by a score of 1-3 on the motor arm item of the NIH Stroke Scale (NIHSS) (Brott et al. 1989) but wrist and finger movement is not required
- No UE injury or conditions that limited use prior to the stroke.
- The patient is >18 years old.
- The patient has subscribed the informed consent
Exclusion Criteria:
- History of epilepsy, brain tumor, major head trauma, learning disorder, severe cognitive impairment, drug or alcohol abuse, major psychiatric illness
- Use of medications that may lower seizure threshold (e.g., metronidazole, fluoroquinolones)
- Severe pain in the affected upper limb (>=8 on the shoulder item of the "joint pain during passive motion" of the Fugl-Meyer Assessment Upper Extremity)
- Further stroke or other significant medical complication during the study
- Evidence of severe leucoencephalopathy (grade IV according to the Fazeka's scale)
- Important aphasia that would impair the understanding and performance of the assessment scales
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 무작위
- 중재 모델: 크로스오버 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: 1 tDCS-Sham
tDC stimulation for 3 weeks, then cross-over to sham stimulation
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Anodal tDCS of the ipsilesional motor cortex and cathodal tDCS of contralesional motor cortex (1.5 mA, 30 minutes) for 15 days during three weeks, then sham stimulation for 30 seconds on 15 days during 3 weeks
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실험적: 2 Sham-tDCS
Sham stimulation for 3 weeks, then cross over to tDCS stimulation
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Sham stimulation for 30 seconds on 15 days during 3 weeks, then anodal tDCS of the ipsilesional motor cortex and cathodal tDCS of contralesional motor cortex (1.5 mA, 30 minutes) for 15 days during three weeks
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가짜 비교기: 3 Sham-Sham
Treatment for 6 weeks daily with sham stimulation
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Sham stimulation for 30 seconds on 15 days during 6 weeks
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Fugl-Meyer Assessment Upper Extremity
기간: 6 weeks
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Investigator administered questionnaire
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6 weeks
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Fugl-Meyer Assessment Upper Extremity
기간: 3 weeks
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Investigator administered questionnaire
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3 weeks
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Fugl-Meyer Assessment Upper Extremity
기간: 6 months
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Investigator administered questionnaire
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6 months
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Barthel Index
기간: 3 weeks
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Investigator administered questionnaire
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3 weeks
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Barthel Index
기간: 6 weeks
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Investigator administered questionnaire
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6 weeks
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Barthel Index
기간: 6 months
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Investigator administered questionnaire
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6 months
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Ashworth scale
기간: 3 weeks
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Investigator administered questionnaire
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3 weeks
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Ashworth scale
기간: 6 weeks
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Investigator administered questionnaire
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6 weeks
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Ashworth scale
기간: 6 months
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Investigator administered questionnaire
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6 months
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Test of Upper Limb Apraxia (TULIA)
기간: 6 weeks
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investigator administered questionnaire
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6 weeks
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Test of Upper Limb Apraxia (TULIA)
기간: 6 months
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investigator administered questionnaire
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6 months
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Grip strength
기간: 3 weeks
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Jamar Hydraulic Hand dynamometer
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3 weeks
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Grip strength
기간: 6 weeks
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Jamar Hydraulic Hand dynamometer
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6 weeks
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Grip strength
기간: 6 months
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Jamar Hydraulic Hand dynamometer
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6 months
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Hamilton depression Rating scale
기간: 6 weeks
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Patient administered questionnaire
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6 weeks
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Hamilton depression Rating scale
기간: 6 months
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Patient administered questionnaire
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6 months
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공동 작업자 및 조사자
협력자
수사관
- 수석 연구원: Carlo Cereda, MD, Ospedale Regionale di Lugano - Civico
간행물 및 유용한 링크
일반 간행물
- Elsner B, Kugler J, Pohl M, Mehrholz J. Transcranial direct current stimulation (tDCS) for improving activities of daily living, and physical and cognitive functioning, in people after stroke. Cochrane Database Syst Rev. 2020 Nov 11;11(11):CD009645. doi: 10.1002/14651858.CD009645.pub4.
- Lindenberg R, Renga V, Zhu LL, Nair D, Schlaug G. Bihemispheric brain stimulation facilitates motor recovery in chronic stroke patients. Neurology. 2010 Dec 14;75(24):2176-84. doi: 10.1212/WNL.0b013e318202013a. Epub 2010 Nov 10.
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
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. .
허혈성 뇌졸중에 대한 임상 시험
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Institut National de la Santé Et de la Recherche...모병
transcranial direct current stimulation (tDCS)에 대한 임상 시험
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University of ChileComisión Nacional de Investigación Científica y Tecnológica; Hospital San Jose; Universidad... 그리고 다른 협력자들완전한
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University of North Carolina, Chapel HillNational Institute of Mental Health (NIMH)완전한
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Hospital Center Guillaume Régnier모병
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Stanford UniversityNYU Langone Health; Wills Eye; Otto-von-Guericke University Magdeburg모집하지 않고 적극적으로
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Shepherd Center, Atlanta GAThe Craig H. Neilsen Foundation완전한