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临床试验/NCT04452019
NCT04452019已完成不适用

Responses on Use of Standing Frame and "Innowalk Pro" in Subacute Patients With Severe Functional Deficits Due to Acquired Brain Injury.

Sunnaas Rehabilitation Hospital1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2020年10月19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
18
试验地点
1
主要终点
Blood pressure

研究概览

简要总结

This study will explore physical and physiological responses to mobilization of patients with acquired brain injuries in subacute phase using a classic standing frame and a standing device with simultaneous passive movement of legs, "Innowalk Pro".

详细描述

Several studies underline the importance of early mobilization of patients with brain injuries, leading to shorter hospital stays, less contractures, and improved general function.

The routine mobilization treatment in the rehabilitation of patients with severe brain injuries in Sunnaas Rehabilitation Hospital is initial use of a tilt table where tilt angle is gradually increased, and when tolerated, standing in a classic standing frame where the patient's lower body is fixed to the device in an upright standing position.

"Innowalk Pro" is a robotic standing device where legs are fixed, but passively moved by electric motors in an upright standing position. An assumption is that standing in "Innowalk Pro" might be better tolerated at an earlier stage of rehabilitation than standing in a classic standing frame.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
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
否

入选标准

  • •Severe brain injury / stroke <1 year post injury.
  • •Medically stable
  • •Paresis in lower extremities, minimal walking function (even with personal assistance) (FIM movement (walk), score 1-2)
  • •Planned stay in Sunnaas RH for a minimum of 2 weeks from time of inclusion
  • •Tolerate 5 minutes in 40 degrees 'upright' position in tilt table (custom orthostasis test)
  • •Body weight ≤95 kg
  • •Body height ≤190 cm

排除标准

  • •Fractures in the lower extremities or in the columna with movement or strain restrictions or with pain.
  • •Aggressive and provocative behavior that affects the ability to collaborate.
  • •Other conditions where upright position is contraindicated

研究组 & 干预措施

"Innowalk Pro"

Experimental

Use of a new device; "Innowalk Pro"

干预措施: Use of a new device; Innowalk Pro (Device)

Standing frame

Active Comparator

Use of standard standing frame

干预措施: Use of standard standing frame (Device)

Standing frame

Active Comparator

Use of standard standing frame

干预措施: Use of a new device; Innowalk Pro (Device)

"Innowalk Pro"

Experimental

Use of a new device; "Innowalk Pro"

干预措施: Use of standard standing frame (Device)

结局指标

主要结局

Blood pressure

时间窗: Up to one week

Blood pressure is monitored continuously

Standing time in minutes

时间窗: Up to one week

Tolerated maximal standing time in each standing device.

次要结局

  • Number of near faints will be registered by the staff.(up to one week)
  • Muscle activity in legs(up to one week)
  • Rate of skin issues(up to one week)
  • Spasticity(up to one week)
  • Perceived exertion(up to one week)
  • Heart rate(up to one week)
  • Number of patients reporting pain(up to one week)

研究者

发起方
Sunnaas Rehabilitation Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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