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临床试验/NCT02701647
NCT02701647已完成不适用

Repetitive Transcranial Magnetic Stimulation Promotes Gait Training in People With Parkinson's Disease - a Randomised Controlled Trial

The Hong Kong Polytechnic University2 个研究点 分布在 1 个国家目标入组 51 人开始时间: 2016年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
51
试验地点
2
主要终点
Fastest Walking Speed

研究概览

简要总结

The purpose of this study is to investigate whether the beneficial effect of treadmill training on people with Parkinson's disease can be enhanced by high- and low-frequency repetitive transcranial magnetic stimulation (rTMS).

详细描述

This is a randomised placebo-controlled trial. Fifty-one participants with Parkinson's disease (PD) will be recruited from the Hong Kong PD association, a self-help group and movement disorders clinic of 3 local hospitals. Written informed consent in accordance with the Declaration of Helsinki will be obtained from all participants. Eligible participants will be randomly assigned into one of the three groups: 1Hz-TT, 25Hz-TT, and sham-TT upon recruitment. Randomisation will be generated by a computer program and group assignment will be blinded to both participants and assessor. Participant will receive either 1-Hz, 25-Hz, or sham rTMS which will last for about 20 minutes followed by 30 minutes treadmill walking training for 12 sessions, 4 times per week for 3 weeks. All assessments will be conducted 1 week before intervention and 1 day after completion of intervention, after 1-month training and at 3-month post training.

The sample size calculation is based on the significant findings of the gait speed reported by Yang et al (2013). A two-way repeated measures ANOVA design with between-subject group effect (3 levels) and within-subject time effect (4 levels) determines that 15 subjects per group are required to achieve 85% power to test the interaction effect between groups and time effect with a 5% significance level and the effect size is 0.2. By assuming 10% dropout rate, 17 subjects will be required per group.

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
Double (Participant, Investigator)

入排标准

年龄范围
40 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with idiopathic Parkinson's disease by a neurologist
  • had been stable on anti-Parkinsonian medication
  • able to walk independently for 30 meters

排除标准

  • severe co-morbidity that may interfere with their ability to participate including significant orthopaedic or rheumatological conditions or disorders of peripheral nervous systems that may interfere with mobility or balance performance
  • a diagnosis of neurological disease other than PD
  • a history of psychiatric disorders
  • the impossibility of inducing motor evoked potentials (MEPs)
  • a score of less than 24 on the Mini-Mental State Examination
  • contraindication to TMS including personal or family history of seizure disorder, metal in the head, implants of medical devices such as cardiac pacemakers or medical pumps, females subjects who are pregnant, a history of neurosurgery
  • subjects with irrepressible tremor and / or dyskinesia

结局指标

主要结局

Fastest Walking Speed

时间窗: Baseline, 1 day post-intervention, 1 month post-intervention, 3 month post-intervention

Each participant is instructed to walk for 14 meters at their fastest walking speed for three trials. The time taken for the middle 10 meter was recorded. The average of three trials is used for analysis.

次要结局

  • Timed-Up-and-Go Test (iTUG)(Baseline, 1 day post-intervention, 1 month post-intervention and 3 months post-intervention)
  • Walking Distance in a 2 -Minute Walk Test(Baseline, 1 day post-intervention, 1 month post-intervention and 3 months post-intervention)
  • Mini Balance Evaluation Systems Test Scores(Baseline, 1 day post-intervention, 1 month post-intervention and 3 months post-intervention)
  • the Motor Section of Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS III)(Baseline, I day post-intervention, 1 month post-intervention and 3 months post-intervention)
  • Dual-task Timed-Up-and-Go Test (DT-TUG)(Baseline, 1 day post-intervention, 1 month post-intervention, 3 month-post intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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