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临床试验/NCT01644929
NCT01644929Unknown不适用

Rehabilitation Combined With Bihemispherictranscranial Direct Current Stimulation in Subacute Ischemic Stroke to Increase Upper Limb Motor Recovery, a Randomised, Controlled, Double-blind Study

Dr. med. Carlo Cereda6 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2013年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
36
试验地点
6
主要终点
Fugl-Meyer Assessment Upper Extremity

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

1 tDCS-Sham

Experimental

tDC stimulation for 3 weeks, then cross-over to sham stimulation

干预措施: transcranial direct current stimulation (tDCS) (Procedure)

2 Sham-tDCS

Experimental

Sham stimulation for 3 weeks, then cross over to tDCS stimulation

干预措施: Sham stimulation, then tDCS (Procedure)

3 Sham-Sham

Sham Comparator

Treatment for 6 weeks daily with sham stimulation

干预措施: Sham stimulation (Procedure)

结局指标

主要结局

Fugl-Meyer Assessment Upper Extremity

时间窗: 6 weeks

Investigator administered questionnaire

次要结局

  • Ashworth scale(6 months)
  • Hamilton depression Rating scale(6 months)
  • Fugl-Meyer Assessment Upper Extremity(6 months)
  • Grip strength(6 months)
  • Barthel Index(6 months)
  • Test of Upper Limb Apraxia (TULIA)(6 months)

研究者

发起方
Dr. med. Carlo Cereda
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Dr. med. Carlo Cereda

Capo clinica

Ospedale Civico, Lugano

研究点 (6)

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