跳至主要内容
临床试验/NCT03144102
NCT03144102Unknown不适用

The Effects of Combining Transcranial Direct Current Stimulation (tDCS) With VR-based Motor Training in Hemiparetic Stroke Patients

Universitat Pompeu Fabra2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2017年5月15日最近更新:
适应症

试验速览

阶段
不适用
入组人数
36
试验地点
2
主要终点
Change of arm/hand function as captured by the upper extremity Fugl-Meyer assessment scale

研究概览

简要总结

Stroke represents one of the main causes of adult disability and will be one of the main contributors to the burden of disease in 2030. However, our healthcare systems do not have enough resources to cover the current demand let alone its future increase. There is a need to deploy new approaches that advance the current rehabilitation methods and enhance their efficiency.

One of the latest approaches used for the rehabilitation of a wide range of deficits of the nervous system is based on virtual reality (VR) applications, which combine training scenarios with dedicated interface devices. On the other hand, recent studies have shown the potential of transcranial direct current stimulation (tDCS) to restore motor function in hemiparetic stroke patients. It must be emphasized, however, that so far little work exists on the quantitative assessment of the clinical impact of VR based approaches in combination with tDCS protocols. We hypothesize that the combination of VR-based motor rehabilitation protocols with concurrent anodal tDCS can boost functional recovery, and may achieve superior effects when compared to 3 alternative treatments: 1) VR without tDCS, 2) occupational therapy with tDCS, and 3) occupational therapy without tDCS.

The findings derived from this study will contribute to establish a novel and superior neurorehabilitation paradigm that can accelerates the recovery of hemiparetic stroke patients. Besides the clinical impact, such achievement could have relevant socioeconomic impact.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Patients with hemiparesis secondary to first ever ischemic or hemorrhagic stroke (Medical Research Council score > 2).
  • Older than 18 years old.
  • Sufficient cognitive capacity to understand and follow the experimental instructions (Mini-Mental State Evaluation > 20).

排除标准

  • Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
  • Epilepsia and metal implants. A diagnostic EEG will be performed by the Department of Clinical Neurophysiology of the hospital to detect epileptic paroxysmal in order to include or exclude patients in the study.
  • Low Cognitive capabilities that prohibits the execution of the experiment Arteriovenous malformation
  • Severe associated impairment such as spasticity, communication disabilities (sensorial, mixed or global aphasia or apraxia), major pain or other neuromuscular impairments or orthopaedic devices that would interfere with the correct execution of the experiment (Modified Ashworth Scale > 3)
  • History of serious mental-health problems in acute or sub acute phase
  • Refusal to sign the consent form
  • Previous surgeries opening the skull.
  • Active or recent substance abuse or dependence within the past year.
  • Pregnancy, breastfeeding, unwillingness to practice birth control during participation in the study.

结局指标

主要结局

Change of arm/hand function as captured by the upper extremity Fugl-Meyer assessment scale

时间窗: At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

次要结局

  • Change of Independence as captured by Barthel scale(At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up))
  • Change of interhemispheric balance as captured by EEG recordings(At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up))
  • Change of motor function in ADLs as captured by Chedoke Arm and Hand Activity Inventory (CAHAI) scale(At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up))
  • Change of spasticity in proximal and distal muscles as captured by Ashworth scale(At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up))
  • Change of spatial hemineglect as captured by the Star cancellation test(At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul Verschure

Prof.

Universitat Pompeu Fabra

研究点 (2)

Loading locations...

相似试验