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临床试验/NCT02053233
NCT02053233已完成不适用

Clinical Trial of Robot-assisted Training for Motor and Gait Recovery in Patients With Stroke

Pusan National University1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2013年6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
入组人数
26
试验地点
1
主要终点
function ambulation category (FAC)

研究概览

简要总结

The robot assisted therapy is one of the new developed technologies for recovery after stroke. This study aimed to evaluating the effect of robotic gait therapy for motor recovery after stroke.

详细描述

This study designed an assessor-blinded, randomized, controlled clinical study. The participations followed the study protocol and were randomly divided into the control group and Walkbot group. The control group received conventional functional rehabilitation for 40 min/session, 2 sessions/day, 5 days/week for 4 weeks, 40 sessions in all. Whereas the Walkbot group received conventional physical therapy (session I for 40 min/day) companied with Walkbot training (session II for 30 min/day) 5 days a week for 4 weeks, 40 session in all. After 4-week intervention all subjects received conventional physical therapy only, 40 min/day, 5 days/week for 4 weeks. During the test period, general rehabilitation and drug treatment can be done at the same time.

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

入选标准

  • The subjects (age>19) with stroke 4 weeks after the onset but within 12 months were included.

排除标准

  • Participated in the clinical studies, or received the rehabilitation therapy or therapy associated with the rehabilitation for the purpose of motor function improvement within thirty days before the start of this study.
  • Cognitive disabilities or serious psychiatric illness.
  • Difficulty in walking due to orthopedic problems.
  • Ejection fraction less than 30% due to severe heart disease or with a diagnosis of unstable angina.
  • Weight more than 135 kg or height less than 150 cm.
  • Pregnancy subjects.

研究组 & 干预措施

Walkbot group

Experimental

The Walkbot group received conventional physical therapy (session I for 40 min/day) companied with Walkbot training (session II for 30 min/day) 5 days a week for 4 weeks, 40 session in all. After 4-week intervention all subjects received conventional physical therapy only, 40 min/day, 5 days/week for 4 weeks.

干预措施: Walkbot group (Device)

control group

Placebo Comparator

The control group received conventional functional rehabilitation for 40 min/session, 2 sessions/day, 5 days/week for 4 weeks, 40 sessions in all. After 4-week intervention all subjects received conventional physical therapy only, 40 min/day, 5 days/week for 4 weeks. During the test period, general rehabilitation and drug treatment can be done at the same time.

干预措施: Control group (Device)

结局指标

主要结局

function ambulation category (FAC)

时间窗: within 4 weeks after robot training

Function ambulation category was used for evaluating gait function. The outcome variable were measured immediately before treatment start (pre-training), 4 weeks after treatment (post-training) and 4 weeks after robot-treatment (follow-up). All the evaluations were done by the same professional therapist who was blind to the two group assignment.

次要结局

  • Berg balance scale (BBS)(within 4 weeks after robot training)
  • Korean modified Barthel index (K-MBI)(within 4 weeks after robot training)

研究者

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

Yong-il Shin

Professor

Pusan National University

研究点 (1)

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