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临床试验/NCT04687293
NCT04687293已完成不适用

Investigation of the Effectiveness of Rehabilitation Using the HUBER 360 Tool to Reduce the Risk of Falls in People in Pathological Situations Requiring Functional Rehabilitation

University of Liege1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2020年12月9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
32
试验地点
1
主要终点
Risk of falls, in seconds

研究概览

简要总结

Aim: The aim of the present study was to analyse the effects of training performed on a rotating, motorised platform (the Huber/SpineForce device from LPG Systems, Valence, France) intended to reduce the risk of falls.

Subjects: any patient 1) benefiting from a physiotherapy rehabilitation program at the CHU Liège, CNRF, Belgium; 2) presenting a pathological situation justifying functional rehabilitation with HUBER 360®; 3) presenting any pathology not constituting an exclusion criterion; 4) giving informed consent to research will be include in this 8-week interventional trial.

Design: randomized open-label trial. Patients will be randomized into the intervention group (HUBER trainig, 45 minutes of training, twice a week during 8 weeks) or in the control group (standard care).

Outcomes: the effect of the training will be measured on the Time-Up-and-Go test, on the Short-Physical performance battery test and on quality of life.

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

性别
All
接受健康志愿者

入选标准

  • Patient benefiting from a physiotherapy rehabilitation program at the CHU Liège, CNRF
  • Patient presenting a pathological situation justifying functional rehabilitation with HUBER 360®
  • Patient presenting any pathology not constituting an exclusion criterion
  • Patient giving informed consent to research.

排除标准

  • Cardiac or respiratory or neurological or rheumatological disease incompatible with physical activity ;
  • Joint inflammation;
  • Rheumatic disease in acute phase;
  • Recent trauma, infection of the musculoskeletal system;
  • Venous thrombosis ;
  • Discopathy in acute phase;
  • Neuropsychological problems that do not allow to integrate the instructions or other serious psychological problems;
  • Cardiovascular diseases and any progressive, chronic, counter-indicative disease;
  • Large anatomical deformities.

研究组 & 干预措施

HUBER

Experimental

HUBER is an isometric strengthening device. It consists of an oval motorized platform, which performs rotating, oscillatory movements with a controlled amplitude and speed.

Intervention will consist of 2 sessions of HUBER per week. Each session lasts approximatively 30 minutes. The intervention is 8 weeks long.

干预措施: HUBER (LPG Systems, France) (Device)

Control

No Intervention

The control group will not received any intervention except usual care.

结局指标

主要结局

Risk of falls, in seconds

时间窗: 8 weeks

Measured with Timed-Up-and Go test

次要结局

  • Quality of life, measured with the Short Form-36 questionnaire(8 weeks)
  • Physical performance(8 weeks)
  • Utility score using the EuroQol- 5 Dimension questionnaire(8 weeks)

研究者

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

Charlotte Beaudart

Principal investigator

University of Liege

研究点 (1)

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