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临床试验/NCT06593184
NCT06593184招募中不适用

Efficacy of Trans-spinal Magnetic Stimulation on Functional Mobility in Chronic Stroke Patients

Universidade Federal de Pernambuco6 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
6
主要终点
Functional Mobility

研究概览

简要总结

The goal of this clinical trial is to learn if trans-spinal magnetic stimulation works to treat gait disorders in chronic stroke adults. It will also learn about the safety of trans-spinal magnetic stimulation.

The main questions it aims to answer are:

Does trans-spinal magnetic stimulation enhance chronic stroke participants gait and functional mobility? Does the technique cause any side effects?

Researchers will compare trans-spinal magnetic stimulation to a sham (a look-alike stimulation with no real effect) to see if trans-spinal magnetic stimulation works to treat gait disorders and improve functional mobility.

Participants will:

Receive trans-spinal magnetic stimulation with treadmill training or a sham stimulation with treadmill training every day for 2 weeks.

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmation of Stroke by digital or physical imaging or medical report
  • Gait impairment
  • Stroke with at least 6 months after ictus

排除标准

  • Metallic implants in spinal cord
  • Major orthopedic/rheumatological disorders
  • Incapacity of verbal or non-verbal communication

结局指标

主要结局

Functional Mobility

时间窗: Enrollment (Day 0); End of treatment (2 weeks); Follow-up after 30 days post-treatment

The Timed-Up and Go (TUG) test is used to evaluate an individual´s capacity to stand up, walk, and sit down. During the test, the participants are timed from the moment they begin to stand up until they are seated again.

次要结局

  • Independency level(Enrollment (Day 0); End of treatment (2 weeks); Follow-up after 30 days post-treatment)
  • Balance(Enrollment (Day 0); End of treatment (2 weeks); Follow-up after 30 days post-treatment)
  • Sensory Function(Enrollment (Day 0); End of treatment (2 weeks); Follow-up after 30 days post-treatment)
  • Spasticity(Enrollment (Day 0); End of treatment (2 weeks); Follow-up after 30 days post-treatment)
  • Lower limb motor function(Enrollment (Day 0); End of treatment (2 weeks); Follow-up after 30 days post-treatment)
  • Perceived change in treatment(End of treatment (2 weeks))

研究者

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

Kátia Monte-Silva

Professor

Universidade Federal de Pernambuco

研究点 (6)

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