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临床试验/NCT07664995
NCT07664995尚未招募不适用

Improving Muscle Strength and Function After Lower Limb Amputation

University of Illinois at Chicago1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2026年7月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
24
试验地点
1

研究概览

简要总结

The goal of this clinical trial is to learn if ischemic conditioning and neuromuscular electrical stimulation improves muscle strength and walking behavior in those with limb loss. The main questions this trial aims to answer are:

Does neuromuscular electrical stimulation improve muscle strength and gait behavior in people who have a leg amputation?

Does neuromuscular electrical stimulation boost the effects of ischemic conditioning on muscle strength and gait behavior in people who have a leg amputation?

Researchers will compare the effects of neuromuscular electrical stimulation to ischemic conditioning to see if there are any significant differences between the impacts of each intervention. Also, researchers will use both interventions together to see if the interventions can boost each other's positive impacts on walking and function in people with leg amputation.

Participants will:

  • Do ischemic conditioning OR neuromuscular electrical stimulation OR both interventions at home every other day for 2 weeks
  • Visit the laboratory before and after completing interventions for the tests
  • Visit the laboratory one week after the post intervention visit for follow-up tests

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

  • Older than 18 years old
  • History of unilateral transfemoral or transtibial amputation
  • Able to ambulate independently without the use of aids (i.e., walking cane)
  • Able to walk at least 6 minutes continuously without stopping.
  • Has a safe residuum with no open wounds on either the residual or intact limb
  • Has a prosthetic limb with materials that are sound and safe to withstand the mobility requirements of the study

排除标准

  • Younger than 18 years old
  • Inability to give informed consent
  • Neurological disorder such as multiple sclerosis that affects gait
  • Currently pregnant (or intend to become pregnant while participating in study)
  • Blood clots in the leg, or any condition in which compression of the thigh or transient ischemia is contraindicated (e.g. open wounds in the leg)
  • History of uncontrolled hypertension
  • History of heart failure
  • Implanted electrical device such as a pacemaker or defibrillator
  • Head injury within the previous 6 months
  • Seizure disorder
  • History of thrombosis
  • History of sickle cell trait
  • History of genetic disease that impacts gait (e.g. cerebral palsy, muscular dystrophy).

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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