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临床试验/NCT07195773
NCT07195773已完成不适用

Effects of Repetitive Transcranial Magnetic Stimulation on Corticomotor Excitability and Balance Performance in People With Parkinson's Disease

Chung Shan Medical University1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2024年12月16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
21
试验地点
1
主要终点
Cortical excitability

研究概览

简要总结

The study investigates the effects of repetitive transcranial magnetic stimulation on motor cortex excitability, balance, and motor function in patients with Parkinson's disease. Additionally, it further examines the effects of single-session low-frequency and high-frequency repetitive transcranial magnetic stimulation on motor cortex excitability.

详细描述

The study investigates the effects of repetitive transcranial magnetic stimulation on motor cortex excitability, balance, and motor function in patients with Parkinson's disease. Additionally, it further examines the effects of single-session low-frequency and high-frequency repetitive transcranial magnetic stimulation on motor cortex excitability.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with primary Parkinson's disease
  • Age: 40-85 years
  • Hoehn and Yahr scale (H&Y scale) : I-III
  • Appropriate prescribed medication, and regular intake for more than 2 weeks
  • Can walk more than 10m with or without the use of assistive devices

排除标准

  • Any other neurological presentation (Excluding PD)
  • Any neurological surgery that would affect participation in this experiment
  • Orthopedic pathology and Cardiovascular issues
  • Exercise used for treatment in the last three months
  • Contraindications for transcranial magnetic stimulation (Presence of metal implants in the head and neck, a pacemaker in the chest, personal or family history of epilepsy, recent brain injury, currently taking antidepressant medication.)

研究组 & 干预措施

Group A

Experimental

Patients in this group first undergo high-frequency rTMS treatment, followed by a two-week rest period, then proceed to low-frequency rTMS after another two-week rest, and finally receive sham stimulation rTMS.

rTMS high-frequency 1Hz 80%RMT rTMS low-frequency 1Hz 80%RMT rTMS sham 10HZ 20%RMT

干预措施: rTMS (Device)

Group B

Experimental

Patients in this group first undergo low-frequency rTMS treatment, followed by a two-week rest period, then proceed to high-frequency rTMS after another two-week rest, and finally receive sham stimulation rTMS.

rTMS high-frequency 1Hz 80%RMT rTMS low-frequency 1Hz 80%RMT rTMS sham 10HZ 20%RMT

干预措施: rTMS (Device)

Group C

Experimental

Patients in this group first undergo sham stimulation rTMS treatment, followed by a two-week rest period, then proceed to high-frequency rTMS after another two-week rest, and finally receive low-frequency rTMS.

rTMS high-frequency 1Hz 80%RMT rTMS low-frequency 1Hz 80%RMT rTMS sham 10HZ 20%RMT

干预措施: rTMS (Device)

结局指标

主要结局

Cortical excitability

时间窗: Cortical excitability will be assessed before and immediately after each intervention. Each intervention is separated by a 2-week washout period. All assessments occur within an 4-week period.

Transcranial magnetic stimulation

Motor function

时间窗: UPDRS-III will be assessed before and immediately after each intervention. Each intervention is separated by a 2-week washout period. All assessments occur within an 4-week period.

UPDRS-III

次要结局

  • Dynamic balance(FRT will be assessed before and immediately after each intervention. Each intervention is separated by a 2-week washout period. All assessments occur within an 4-week period.)
  • Functional mobility(TUG will be assessed before and immediately after each intervention. Each intervention is separated by a 2-week washout period. All assessments occur within an 4-week period.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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