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临床试验/NCT02345525
NCT02345525已完成不适用

The Feasibility of a Home-based Constraint-Induced Movement Therapy Program in Chronic Stroke Survivors.

University Hospital of Ferrara2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年8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
20
试验地点
2
主要终点
Changes from baseline in Fugl-Meyer Upper Extremity (FM-UE)

研究概览

简要总结

The aim of this study is to evaluate the feasibility of a Home-based Constraint-Induced Movement Therapy (hCIMT) compared to a Modified Constraint-Induced Movement Therapy (mCIMT) delivered in a outpatient setting on upper limb motor recovery in stroke survivors.

详细描述

Home-based Constraint Induced Modified Therapy (hCIMT) consist of 2 hours intensive upper limb practice with shaping techniques + 2 hours ADLs supervised by a caregiver. Patients are supposed to wear a mitt on the unaffected hand for 4 hours daily.

Modified Constraint Induced Modified Therapy (mCIMT) consist of 2 hours intensive upper limb practice with shaping techniques supervised by an experienced physiotherapist + 2 hours ADLs at home (supervised by a caregiver) Patients are supposed to wear a mitt on the unaffected hand for 4 hours daily.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age > 18 years and < 80 years
  • diagnosis of first ischemic stroke
  • stroke onset > 6 months prior to study enrollment
  • upper extremity hemiparesis with impairment of hand and/or arm:
  • active wrist extension ≥20º
  • active metacarpophalangeal- and interphalangeal-joints extension ≥ 10°
  • muscle tone assessed by the Modified Ashworth Scale (MAS) ≤ 2
  • pain assessed by the Visual Analogue Scale (VAS) <4

排除标准

  • anyone who does not have adequate understanding of verbal or written information in Italian sufficient to complete any test
  • impaired cognitive functioning: score less than 24 on the Mini Mental Status Examination (MMSE)
  • contraindications to single-pulse transcranial magnetic stimulation (TMS)(TMS will be used to measure cortical excitability): presence of a history of epilepsy, frequent headaches or neck pain, implantable devices (ventriculoperitoneal shunts, pacemakers, intrathecal pumps, intracranial metal implants)
  • neurological or psychiatric pathology
  • severe cardio-pulmonary, renal, hepatic diseases
  • pregnancy

研究组 & 干预措施

mCIMT

Active Comparator

2 hours intensive upper limb practice with shaping techniques supervised by an experienced physiotherapist + 2 hours ADLs at home (supervised by a caregiver) Patients are supposed to wear a mitt on the unaffected hand for 4 hours daily.

干预措施: mCIMT (Behavioral)

hCIMT

Experimental

2 hours intensive upper limb practice with shaping techniques + 2 hours ADLs supervised by a caregiver.

Patients are supposed to wear a mitt on the unaffected hand for 4 hours daily.

干预措施: hCIMT (Behavioral)

结局指标

主要结局

Changes from baseline in Fugl-Meyer Upper Extremity (FM-UE)

时间窗: 1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up

Measure of upper extremity motor impairment. The upper extremity score ranges from 0-66.

次要结局

  • Wolf Motor Function Test (WMFT)(1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up)
  • Nine Hole Peg Test (NHPT(1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up)
  • Motor Activity Log (MAL)(1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up)
  • Motor cortex excitability (single pulse and paired pulse TMS)(1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up)
  • Stroke Impact Scale 3.0 (SIS 3.0)(1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up)
  • NIRS (Near Infrared Spectroscopy) NIRS measurements will be performed during 6 cycles of 15s hand reaching and grasping and 45s resting while sitting on a chair.(1)A week prior to treatment beginning 2) the week after the end of treatment 4) at 3 months follow-up)

研究者

发起方
University Hospital of Ferrara
申办方类型
Other
责任方
Sponsor

研究点 (2)

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