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临床试验/NCT05225792
NCT05225792招募中不适用

Improved Training Method for Advanced Rehabilitation of Warfighters With Lower Extremity Trauma

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年1月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
Mayo Clinic
入组人数
40
试验地点
1
主要终点
Prosthesis Evaluation Questionnaire-Addendum (PEQ-A)

研究概览

简要总结

The purpose of this study is to find out if an advance balance perturbation training program can enhance the rehabilitation process by increasing weight-bearing strategies on the prosthetic or injured limb, and, help reduce stumbles and falls.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

  • Research participants will be eligible active duty service members and retired veterans.
  • Having lower limb trauma (transtibial and transfemoral amputations, bilateral amputations, and limb salvage).
  • Are enrolled in conventional rehabilitation at the participating military treatment centers.
  • Subjects with dysvascular disease will be excluded because compromised lower limb somatosensation and circulation are independently linked with poor postural stability and a history of frequent falls.
  • For subjects with amputations, the individual must be a community ambulator (i.e., K-Level 3 or 4).
  • For subjects with limb salvage, they will need to have an IDEO and be entered into the Return-to-Run training program.

排除标准

  • - Subjects must not have excessive pain or other neuromuscular problems that preclude them from performing the test protocol.

研究组 & 干预措施

Injured Service Members

Experimental

干预措施: Promis Physical Function Questionnaire (Behavioral)

Injured Service Members

Experimental

干预措施: L Test (Behavioral)

Injured Service Members

Experimental

干预措施: Narrowing Beam Walking Test (Behavioral)

Injured Service Members

Experimental

干预措施: PEQ-A (Behavioral)

结局指标

主要结局

Prosthesis Evaluation Questionnaire-Addendum (PEQ-A)

时间窗: 0, 6 months

Fall incidence change between baseline and 6 months

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kenton R. Kaufman, PhD, PE

Principal Investigator

Mayo Clinic

研究点 (1)

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