跳至主要内容
临床试验/NL-OMON47150
NL-OMON47150已完成不适用

Validation of a prosthetic leg prototype aimed at increasing lateral balance control in prosthetic walking: a pilot study - Lateral Balance in Prosthetic Walking

niversitair Medisch Centrum Groningen0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Amputee subjects (patients):
  • - written informed consent;
  • - Unilateral transfemoral amputation;
  • - Between 18 - 80 years old;
  • - Daily prosthetic use for at least one year;
  • - Mobility level at least 3 (as judged by medical professional);
  • - Ability to walk independently for an hour, e.g. without the use of walking aids;
  • - Clearance under prosthetic knee at least 35cm. ;Able-bodied reference group:
  • - Age matched with amputee group.

排除标准

  • Self reported criteria of:
  • - Serious vascular problems or pain of the non-amputated limb;
  • - Musculoskeletal dysfunctions or disease (other than the amputation for amputees);
  • - Serious cardiac or pulmonary problems;
  • - Diseases that interfere with equilibrium (other than the amputation for amputees);
  • - Serious visual problems;
  • - Amblyacousia;
  • - Otitis media;
  • - Use of antipsychotic, sedative or antidepressant drugs (except amitriptyline);
  • - Use of other medication that interfere with equilibrium or cognition;
  • - Inability to cope with the new prosthetic set-up (see 7.3 and 7.7 of the research protocol).

研究者

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