跳至主要内容
临床试验/NCT06837363
NCT06837363招募中不适用

A Multicenter Confirmation Clinical Trial of Untact Upper Extremity Rehabilitation Using Smart Board for Late Subacute and Chronic Patients With Brain Disorder - a Randomized Single-blinded Controlled Trial

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年4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
招募中
入组人数
40
试验地点
1
主要终点
Improvement of uper limb score in Fugl-Meyer assessment

研究概览

简要总结

The aim is to clinically validate the clinical efficacy, usability, and safety of home-based upper limb rehabilitation training using the Neofect Smart Board by comparing the effects between a group using the home-based Neofect Smart Board and a group performing conventional home-based occupational therapy in patients with upper limb dysfunction in the late subacute and chronic stages of neurological diseases.

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
19 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with neurological diseases aged 19 to 85 years old
  • •Patients with hemiparesis lasting for more than 3 months due to neurological diseases (stroke, traumatic brain injury, brain tumor) and impaired upper limb function
  • •Patients with shoulder flexor and adductor muscle strength of MRC grade 2 or higher
  • •Patients with shoulder extensor and abductor spasticity of MAS grade 1+ or lower
  • •Participants with sufficient cognitive function to understand the instructions from the researcher and the smart board, and to perform the tasks (K-MMSE ≥21)

排除标准

  • •pre-existing significant neurogenic disorders
  • •major psychiatric disorders such as schizophrenia, bipolar disorder, or dementia
  • •History of diseases that caused pain or muscle atrophy in the affected upper limb before the onset of the neurological disease, which interfered with rehabilitation
  • •Severe spasticity of the affected upper limb (Modified Ashworth Scale score ≥3)
  • •skin disorders or open wounds on the affected upper limb
  • •Amputation, fractures, or soft tissue-related diseases or injuries on the affected upper limb
  • •severe pain that interferes with rehabilitation of the affected upper limb (Numeric Rating Scale > 6)
  • •Inability to maintain a seated posture for more than 10 minutes, which is required for using the smart board
  • •Significant visual impairment to the extent that the screen cannot be recognized when using the smart board

研究组 & 干预措施

Home-based Neofect Smart Board

Experimental

home-based upper limb rehabilitation training using the Neofect Smart board

干预措施: Home-based Neofect Smart board (Device)

home-based occupational therapy

Active Comparator

home-based upper limb rehabilitation training using the workbook provided by the research team

干预措施: home-based occupational therapy (Other)

结局指标

主要结局

Improvement of uper limb score in Fugl-Meyer assessment

时间窗: Within 14 days before the intervention, within 2 days after intervention

(upper limb motor score in Fugl-Meyer assessment at post-intervention) - (upper limb motor score in Fugl-Meyer assessment at baseline) Higher scores mean a better outcome

次要结局

未报告次要终点

研究者

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

Won Hyuk Chang

Professor

Samsung Medical Center

研究点 (1)

Loading locations...

相似试验