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临床试验/NCT04281394
NCT04281394已完成不适用

Effects of Robot-assisted Gait Training in Patients Burn Injury on Lower Extremity : a Randomized Controlled Trial

Hangang Sacred Heart Hospital2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2019年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
2
主要终点
the changes of functional ambulatory category

研究概览

简要总结

Gait enables individuals to move forward and is considered a natural skill. However, gait disturbances are very common in patients with burn injury. Major causes of functional impairment are pain and joint contractures. Recent studies focused on the application of robot-assisted gait training (RAGT). This study aimed to elucidate the efficacy and investigate the mechanism of motor recovery after RAGT on patients with lower extremity burn.

详细描述

This study aimed to elucidate the efficacy and investigate the mechanism of motor recovery after RAGT on patients with lower extremity burn.

20 patients with burn were randomly divided into 2 groups. RAGT group received RAGT 5 sessions per week at duration 30 minutes with 30 minutes conventional physical therapy in 12 weeks. SUBAR® (CRETEM, Korea) is a wearable robot with a footplate that assists patients to perform voluntary muscle movements. The conventional group underwent conventional physical therapy twice a day, 5 times a week in 12 weeks. Main outcomes were functional ambulatory category(FAC), 6 minutes walking test(6MWT), visual analogue scale(VAS), isometric forces of bilateral knee and ankle muscles, and foot pressure analysis before and after 12 weeks training.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with full or virtually full thickness involvement of >50% on the body surface area of the lower extremity
  • age > 18 years
  • with ≤1 functional ambulation category (FAC) score ≤ 3

排除标准

  • patients with cognitive disorders before burn
  • serious cardiac dysfunction
  • problems with weight bearing due to unstable fractures
  • body weight ≥100 kg
  • severe fixed contracture
  • skin disorders that could be worsened by RAGT and conventional rehabilitation
  • patients with severe pain who were unable to undergo conventional rehabilitation programs.

结局指标

主要结局

the changes of functional ambulatory category

时间窗: baseline, and after 12 weeks intervention

Scale 0 means that the patient cannot walk or can only walk with assistance of two people. Scale 5 means that the patient can walk independently. Higher scores mean a better outcome.

the changes of 6 minutes walking test

时间窗: baseline, and after 12 weeks intervention

6MWT was performed in accordance with standardized guidelines, and the walking course was 20 m. Patients were instructed to walk as far as possible in 6 min. Higher scores mean a better outcome.

the changes of visual analogue scale

时间窗: baseline, and after 12 weeks intervention

Visual analogue scale was used to rate the degree of subjective pain during gait movement: 0 points were assigned when no pain was noted, and unbearable pain was assigned 10 points. higher scores mean a worse outcome

次要结局

  • the changes of gait symmetry using stride length(baseline, and after 12 weeks intervention)
  • the changes of center of foot pressure pattern(baseline, and after 12 weeks intervention)
  • the changes of active range of motion of dorsiflexion and plantarflexion(baseline, and after 12 weeks intervention)
  • the changes of isometric forces of knee flexion and knee extension(baseline, and after 12 weeks intervention)
  • the changes of isometric forces of ankle dorsiflexion and ankle plantarflexion(baseline, and after 12 weeks intervention)
  • the changes of active range of motion of flexion and extension(baseline, and after 12 weeks intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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