跳至主要内容
临床试验/NCT05919043
NCT05919043已完成不适用

Upper Limb-based Movement Priming for Lower Limb Neuroplasticity & Motor Recovery in Stroke

University of Illinois at Chicago1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2024年7月1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
17
试验地点
1
主要终点
Spinal H-reflex excitability using peripheral nerve stimulation (PNS)

研究概览

简要总结

The goal of this clinical trial is to to determine the effect of movement-based priming using the upper limbs on lower limb neuroplasticity and behaviors in chronic stroke.

The main questions we aim to answer are:

  1. What are the acute effect of UL-priming on lower limb neuroplasticity and motor behaviors in persons with stroke compared to other priming modalities?
  2. What are the time effects of UL-priming on neuroplasticity and motor behavior in individuals with stroke?

In this cross over study, participants will be involved in three priming sessions involving

- UL-priming using rhythmic, symmetric, bilateral priming involving the movement of at least one major joint in the upper limbs.

AND

- Sham priming using auditory stimulation (1 Hz metronome).

AND

- Lower-limb movement-based priming using rhythmic, symmetric, dorsiflexion and plantarflexion movements.

Researchers will compare outcome measures between the different priming sessions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Single, monohemispheric stroke
  • •Chronic stroke (> 6 months prior)
  • •Residual hemiparetic gait deficits (e.g., abnormal gait pattern)
  • •Minimum score of stage 2 on the Chedoke Arm Impairment Scale which includes stage 2, task 3 (facilitated elbow flexion) as one of the stage 2 tasks.

排除标准

  • •Use of anti-spasticity medications
  • •Existence of other neurological disorders
  • •Have brainstem or cerebellar lesions.
  • •Score of ≥2 on the Modified Ashworth Scale.
  • •MMSE score of <21, to ensure they will follow instructions.
  • •Non-English-speaking individuals
  • •Bone, joint or soft tissue injury
  • •Uncontrolled medical conditions (such as uncontrolled hypertension, untreated cardiac disease, or untreated pulmonary disease)
  • •No Motor evoked potentials (MEPs) during TMS
  • •TMS exclusion criteria
  • •Previous adverse reaction to TMS
  • •Skull abnormalities or fractures
  • •Concussion within the prior 6 months
  • •Unexplained, recurring headaches
  • •Implanted cardiac pacemaker
  • •Metal implants in the head or face
  • •History of seizures or epilepsy
  • •Use of medications that could alter cortical excitability or increase risk of seizure (e.g., antidepressants, antipsychotics, anxiolytics, anticonvulsants)
  • •Current pregnancy

研究组 & 干预措施

Lower limb-based movement priming (LL-priming)

Active Comparator

Participants will perform rhythmic, symmetric, bilateral plantarflexion and dorsiflexion movements.

干预措施: Lower limb-based movement priming (LL-priming) (Other)

Upper limb-based movement priming (UL-priming)

Experimental

The upper limb priming task will include rhythmic, bilateral priming involving the movement of at least one major joint in the upper limbs (shoulder, elbow, wrist).

干预措施: Upper limb-based movement priming (UL-priming) (Other)

Sham priming

Sham Comparator

Participants will listen to a 1 Hz metronome for 20 minutes as a form of auditory stimulation during the sham priming session.

干预措施: Sham priming (Other)

结局指标

主要结局

Spinal H-reflex excitability using peripheral nerve stimulation (PNS)

时间窗: Change from baseline to immediately after priming and to 24 hours after priming.

Peripheral nerve stimulation (PNS) will be used to assess the H reflexes excitability from the soleus muscles.

Corticomotor excitability using transcranial magnetic stimulation (TMS)

时间窗: Change from baseline to immediately after priming and to 24 hours after priming.

Single-pulse transcranial magnetic stimulation (TMS) will be used to assess the corticomotor excitability from the tibialis anterior and soleus muscles.

Muscle Strength

时间窗: Change from baseline to immediately after priming and to 24 hours after priming.

An estimate of maximum ankle muscle force will be obtained for three trials of dorsiflexion and plantarflexion contractions using a force transducer and EMG.

次要结局

未报告次要终点

研究者

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

Sangeetha Madhavan

Professor, Physical Therapy

University of Illinois at Chicago

研究点 (1)

Loading locations...

相似试验