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临床试验/NCT03349138
NCT03349138已完成不适用

Integrated Cognitive, Sensory, and Motor Rehabilitation of Hand Functions

Villa Beretta Rehabilitation Center2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2015年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Motricity Index

研究概览

简要总结

This study evaulates the addition to the standard theraphy of enriched sensorimotor training by means of robotic glove therapy, or functional electrical stimulation in the treatment of chronic stroke patients with upper limb motor impairments. All the patients receive the conventional physiotherapic treatment. Supplemental to the conventional treatment, patients are evenly split in four groups to provide different treatments for an equivalent amount of time. Patient in the first group receive supplemental conventional therapy; patients in the second group receive robotic glove therapy; patients in the third group receive functional electrical stimulation; patients in the fourth group receive robotic glove treatment and functional electrical stimulation in different sessions.

详细描述

Stroke very frequently impacts on patients' motor function, and particularly on upper limb movements. Limited hand functionality is a major negative outcome after stroke, negatively affecting patients' recovery and independence, with major impact on rehabilitation.However, standard motor rehabilitation outcome is often suboptimal, because insufficient or non-specific treatment is provided. Robotic hand mobilization and functiona electrical stimulation grasp rehabilitation each improve motor capabilities in grasp impaired patients, but they do so by different mechanisms.

Robotic hand mobilization achieves grasp rehabilitation by providing passive mobilization of the affected limb if the subject does not react to the designed task.

Functional electrical stimulation achieves grasp rehabilitation by inducing localized muscle contraction, that is by providing an electrical field able to stimulate both sensory afferent pathways and lower motor neurons in the targeted volume.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults male and/or female, older than 18 years
  • Patients who have suffered one or more strokes with major unilateral functional impairment
  • Hemiplegic, left and right unilateral lesion
  • Chronic phase of stroke at least six months before study enrollment
  • Level of impairment: hand and/or arm
  • No left handed
  • Mini-Mental State Examination > 20

排除标准

  • Limitation for using the device due to impairment of Passive Range of Motion and/or
  • Pain due to Spasticity evaluated using Modified Ashworth Scale (>=3)
  • Previous history of major neurological or psychiatric disorders
  • allergy to electrodes

研究组 & 干预措施

Conventional Therapy

Active Comparator

27 sessions, 3 sessions per week for a total of 9 weeks. Each session lasts about 90 minutes and consists of different standard motor training modalities typically used in the rehabilitation of the arm after stroke. The training session is customized on the patients' need and can be adapted to their improvement during the intervention.

干预措施: Conventional Therapy (Device)

Robotic Glove

Experimental

Robotic Glove & Conventional Therapy 27 sessions, 3 sessions per week for a total of 9 weeks. Each session consists of 30-minute training with the robotic glove system plus 60 minutes of conventional therapy. The training session is customized on the patients' need and can be adapted to their improvement during the intervention.

干预措施: Robotic Glove (Device)

Electrical Stimulation

Experimental

Electrical Stimulation & Conventional Therapy 27 sessions, 3 sessions per week for a total of 9 weeks. Each session consists of 30-minute training with the electrical stimulation system plus 60 minutes of conventional therapy. The training session is customized on the patients' need and can be adapted to their improvement during the intervention.

干预措施: Electrical Stimulation (Device)

Electrical Stimulation and Robotic Glove

Experimental

Electrical Stimulation & Robotic Glove & Conventional Therapy 27 sessions, 3 sessions per week for a total of 9 weeks. Each session consists of 30-minute training with the electrical stimulation system plus 60 minutes of conventional therapy or 30-minute training with the robotic glove system plus 60 minutes of conventional therapy. Half of the sessions are allocated to the electrical stimulation system, and half are allocated to the robotic glove system. The training session is customized on the patients' need and can be adapted to their improvement during the intervention.

干预措施: Robotic Glove (Device)

Electrical Stimulation and Robotic Glove

Experimental

Electrical Stimulation & Robotic Glove & Conventional Therapy 27 sessions, 3 sessions per week for a total of 9 weeks. Each session consists of 30-minute training with the electrical stimulation system plus 60 minutes of conventional therapy or 30-minute training with the robotic glove system plus 60 minutes of conventional therapy. Half of the sessions are allocated to the electrical stimulation system, and half are allocated to the robotic glove system. The training session is customized on the patients' need and can be adapted to their improvement during the intervention.

干预措施: Electrical Stimulation (Device)

结局指标

主要结局

Motricity Index

时间窗: 9 weeks

Outcome measure to evaluate motor impairment after stroke; subscale for arm only; the subscale ranges from 0 (maximal impairment) to 100 (no impairment).

次要结局

  • Motor Activity Log(baseline; 9 weeks; 13 weeks.)
  • Action Research Arm Test(baseline; 9 weeks; 13 weeks.)
  • Medical Research Council(baseline, 9 weeks, 13 weeks.)
  • Box & Blocks Test(baseline; 9 weeks; 13 weeks.)
  • Modified Ashworth Scale(baseline; 9 weeks; 13 weeks)

研究者

发起方
Villa Beretta Rehabilitation Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Franco Molteni

Clinical Director

Villa Beretta Rehabilitation Center

研究点 (2)

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