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.
調査の概要
状態
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
研究場所
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Bern、スイス、3010
- 引きこもった
- Universitätsspital Bern, Inselspital, Neuropsychologische Rehabilitation
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Brissago、スイス、6614
- 募集
- Clinica Hildebrand, Centro di riabilitazione Brissago
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コンタクト:
- Paolo Rossi, MD
- 電話番号:+41 91 786 86 86
- メール:p.rossi@clinica-hildebrand.ch
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主任研究者:
- Paolo Rossi, MD
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Zihlschlacht、スイス、8588
- 終了しました
- HELIOS Klinik Zihlschlacht AG, Neurologisches Rehabilitationszentrum
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:他の
- 割り当て:ランダム化
- 介入モデル:クロスオーバー割り当て
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的: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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実験的: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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偽コンパレータ: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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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Fugl-Meyer Assessment Upper Extremity
時間枠:6 weeks
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Investigator administered questionnaire
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6 weeks
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Fugl-Meyer Assessment Upper Extremity
時間枠:3 weeks
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Investigator administered questionnaire
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3 weeks
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Fugl-Meyer Assessment Upper Extremity
時間枠:6 months
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Investigator administered questionnaire
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6 months
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Barthel Index
時間枠:3 weeks
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Investigator administered questionnaire
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3 weeks
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Barthel Index
時間枠:6 weeks
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Investigator administered questionnaire
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6 weeks
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Barthel Index
時間枠:6 months
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Investigator administered questionnaire
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6 months
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Ashworth scale
時間枠:3 weeks
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Investigator administered questionnaire
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3 weeks
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Ashworth scale
時間枠:6 weeks
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Investigator administered questionnaire
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6 weeks
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Ashworth scale
時間枠: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)
時間枠: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)
時間枠:6 months
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investigator administered questionnaire
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6 months
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Grip strength
時間枠:3 weeks
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Jamar Hydraulic Hand dynamometer
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3 weeks
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Grip strength
時間枠:6 weeks
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Jamar Hydraulic Hand dynamometer
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6 weeks
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Grip strength
時間枠:6 months
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Jamar Hydraulic Hand dynamometer
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6 months
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Hamilton depression Rating scale
時間枠:6 weeks
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Patient administered questionnaire
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6 weeks
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Hamilton depression Rating scale
時間枠:6 months
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Patient administered questionnaire
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6 months
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協力者と研究者
スポンサー
協力者
捜査官
- 主任研究者:Carlo Cereda, MD、Ospedale Regionale di Lugano - Civico
出版物と役立つリンク
一般刊行物
- 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.
研究記録日
主要日程の研究
研究開始
一次修了 (予想される)
研究の完了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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