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临床试验/NCT02656316
NCT02656316Unknown不适用

The Effects of Multi-focal Transcranial Direct Current Stimulation (tDCS) on Motor-cognitive Dysfunctions and Freezing of Gait in Patients With Parkinson's Disease: A Randomized Controlled Trial

Tel-Aviv Sourasky Medical Center2 个研究点 分布在 1 个国家目标入组 85 人开始时间: 2017年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
85
试验地点
2
主要终点
Changes in frequency and severity of the freezing of gait phenomenon

研究概览

简要总结

The current RCT aims to establish the therapeutic potential of tDCS for freezing of gait (FOG) and motor-cognitive dysfunctions in PD. As noted, FOG is often unresponsive to pharmacological and other treatments, especially in the advanced stages of the disease. While it is likely that tDCS will provide symptomatic relief, we will also explore, via secondary outcomes, the potential for tDCS to modify disease progression. Support for this possibility stems from the likely mechanisms of action of tDCS.

详细描述

The current study aim to establish the therapeutic potential of tDCS for freezing of gait (FOG) and motor-cognitive dysfunctions in Parkinson's Disease (PD). FOG phenomenon is often unresponsive to pharmacological and other treatments, especially in the advanced stages of the disease. While it is likely that Transcranial direct current stimulation (tDCS) will provide symptomatic relief, we will also explore, via secondary outcomes, the potential for tDCS to modify disease progression. Support for this possibility stems from the likely mechanisms of action of tDCS.

Based on strong rationale and preliminary findings in previous works, the objectives of the current proposal are to conduct a prospective multi-center, double-blinded, stratified controlled randomized clinical trial, comparing real multifocal tDCS to sham stimulation. The main aim:

  • To demonstrate the "short-term" and the longer-term effects of tDCS on FOG severity and frequency.

Participants: A total of 85 patients will be recruited (Hoehn and Yahr Stage 1-3.5) who suffer from FOG, as measured by the new FOG questionnaire (NFOG-Q) and as demonstrated in response to a FOG provoking protocol, who are on stable medications, who have no contraindications to tDCS, and who are between the ages of 40-80. Patients with DBS will not be included.

tDCS intervention: Subjects will be randomized to receive either a real or sham tDCS intervention. Each intervention will consist of 10, 20-minute treatments completed over 2 consecutive weeks (i.e., 5 per week), following previously established protocols. A single, weekly "maintenance" treatment will then be provided for the following 12 weeks (note: for depression, maintenance tDCS is most often provided once every two weeks; we will take a more conservative approach here in this first long-term study for FOG in PD).

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, Investigator)

入排标准

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

入选标准

  • Inclusion criteria: patients diagnosed with PD, with Hoehn and Yahr Stage between 1-3.5, who suffer from FOG, as measured at screening by the previously validated new FOG questionnaire (NFOG-Q), whose medications have not changed within 1 month of the study and are not anticipated to change during the study, are able to walk independently, and who are between the ages of 40-80 inclusive.

排除标准

  • Subjects who show no FOG during testing in the lab in response to a FOG provoking protocol, any diagnosed psychiatric or other neurological disorder, stroke, unbalanced and high blood pressure, pregnancy, participation in any clinical trial in the last three months, unwillingness to be randomized; implanted with deep brain stimulation, pacemakers, intracranial electrodes, implanted defibrillators or any other prosthesis; or a perceived inability to complete the study. Additional exclusion criteria related to tDCS safety will include a personal or family history of epilepsy, the use of neuro-active drugs, or risk of metal fragments in the eyes or head.

研究组 & 干预措施

Active tDCS

Experimental

The active tDCS condition will consist of 20 min of continuous stimulation. This amount of stimulation is safe for healthy young and older adults and has been shown to induce acute beneficial changes in cortical excitability and cognitive functions.

干预措施: Active tDCS (Device)

Sham tDCS

Sham Comparator

The Sham tDCS - an inactive stimulation.

干预措施: Sham tDCS (Device)

结局指标

主要结局

Changes in frequency and severity of the freezing of gait phenomenon

时间窗: short (two weeks) after treatment and long term following (11 weeks) after treatment

Clinical assessment of freezing of gait: Gait tasks to provoke FOG (e.g. gait trajectory with dual tasking).

次要结局

  • Changes in cognitive performance(short (two weeks) after treatment and long term following (11 weeks) after treatment)
  • Immediate change in gait mesurments(short (two weeks) after treatment and long term following (11 weeks) after treatment)

研究者

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

michal roll

Director of Research and Developmen

Tel-Aviv Sourasky Medical Center

研究点 (2)

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