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临床试验/NCT01404039
NCT01404039终止1 期

Investigating Motor Cortex Processing for Pain Modulation

Spaulding Rehabilitation Hospital1 个研究点 分布在 1 个国家目标入组 115 人开始时间: 2010年9月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
终止
发起方
入组人数
115
试验地点
1
主要终点
Change in Motor Cortex Excitability MEP Amplitude

研究概览

简要总结

The purpose of this study is to investigate the effects of different types of interventions (motor learning, somatosensory learning, observation task, mental imagery and tDCS) on the perception of pain and motor cortex excitability in healthy male subjects. This is an exploratory study of healthy subjects only.

详细描述

There are 5 experiments:

Exp1: motor learning (3 groups, crossover) - motor leaning with and without visual feedback and a control group.

Exp2: sensory learning (4 groups, parallel) - sensory learning with and without feedback, an simple activation task and a control group.

Exp3: observational task (2 groups, parallel) - an motor observational task and a control group.

Exp4: mental imagery (2 groups, parallel) - a motor mental imagery and a control group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •Provide informed consent to participate in the study
  • •18 to 64 years old
  • •No presence of rheumatologic disease as self reported
  • •No clinically significant or unstable medical or psychiatric disorder as self reported
  • •No history of alcohol or substance abuse within the last 6 months as self reported
  • •No neuropsychiatric co-morbidity as self reported
  • •No Contraindications to single pulse TMS (TMS will be used to measure cortical excitability)
  • •history of seizures
  • •unexplained loss of consciousness
  • •metal in the head
  • •frequent or severe headaches or neck pain
  • •implanted brain medical devices
  • •No Contraindications to tDCS
  • •metal in the head
  • •implanted brain medical devices

排除标准

  • 未提供

研究组 & 干预措施

Motor Learning (ML) sighted

Experimental

In this arm, subject will perform motor Learning with visual feedback - ML sighted.

There will be an anticipated total of 15 subjects in this experimental arm. This arm will be conducted as a cross-over design. The subjects will undergo the three interventions listed (motor learning with visual feedback, motor learning without visual feedback, and control group) in a counterbalanced randomized order. There will be at least 24 hours between each experimental session.

干预措施: Motor Learning (Behavioral)

Motor Learning (ML) blind

Experimental

In this arm, subject will perform motor Learning without visual feedback - ML blind.

There will be an anticipated total of 15 subjects in this experimental arm. This arm will be conducted as a cross-over design. The subjects will undergo the three interventions listed (motor learning with visual feedback, motor learning without visual feedback, and control group) in a counterbalanced randomized order. There will be at least 24 hours between each experimental session.

干预措施: Motor Learning (Behavioral)

Motor Learning (ML) control group

Placebo Comparator

In this arm, subject will perform simple hand movements - control group. There will be an anticipated total of 15 subjects in this experimental arm. This arm will be conducted as a cross-over design. The subjects will undergo the three interventions listed (motor learning with visual feedback, motor learning without visual feedback, and control group) in a counterbalanced randomized order. There will be at least 24 hours between each experimental session.

干预措施: Motor Learning (Behavioral)

Somatosensory Learning (SL sighted)

Experimental

In this arm, subject will perform sensory Learning with visual feedback - SL sighted.

There will be an anticipated total of 10 subjects in this experimental arm. This experimental arm will be conducted in a parallel design with 4 groups (SL sighted, SL blind, Sactivation, SL control).

干预措施: Somatosensory Learning (Behavioral)

Somatosensory Learning (SL blind)

Experimental

In this arm, subject will perform sensory Learning without visual feedback - SL blind.

There will be an anticipated total of 10 subjects in this experimental arm. This experimental arm will be conducted in a parallel design with 4 groups (SL sighted, SL blind, Sactivation, SL control).

干预措施: Somatosensory Learning (Behavioral)

Somatosensory Activation (S activation)

Experimental

In this arm, subject will receive simple sensory stimulation over their left index finger - Sactivation.

There will be an anticipated total of 10 subjects in this experimental arm.This experimental arm will be conducted in a parallel design with 4 groups (SL sighted, SL blind, Sactivation, SL control).

干预措施: Somatosensory Learning (Behavioral)

Somatosensory Learning (SL) control group

Placebo Comparator

In this arm,the subjects will not receive any somatosensory input (SL control group).

There will be an anticipated total of 10 subjects in this experimental arm. This experimental arm will be conducted in a parallel design with 4 groups (SL sighted, SL blind, Sactivation, SL control).

干预措施: Somatosensory Learning (Behavioral)

Observational Task (OT) - real

Experimental

In this arm, the subjects will perform an observational task - observation of hand movements. This experimental arm will be conducted in a parallel design. There will be 15 subjects per intervention.

干预措施: Observational Task (Behavioral)

Observational Task (OT) - control group

Placebo Comparator

In this arm, the subjects will perform a controlled observational task - observation of geometric shapes. This experimental arm will be conducted in a parallel design. There will be 15 subjects per intervention.

干预措施: Observational Task (Behavioral)

Mental Imagery (MI) - real

Experimental

In this arm, the subjects will perform mental imagery - mental imagery of finger movements. This experimental arm will be conducted in a parallel design. There will be 15 subjects per intervention.

干预措施: Mental Imagery (Behavioral)

Mental Imagery (MI) - control group

Placebo Comparator

In this arm, the subjects will perform a controlled task - simple mental calculation. This experimental arm will be conducted in a parallel design. There will be 15 subjects per intervention.

干预措施: Mental Imagery (Behavioral)

transcranial direct current stimulation - tDCS real

Experimental

tDCS will be applied over the motor cortex for 20minutes at an intensity of 2mA. 15 subjects will be enrolled. The subjects will undergo two interventions, real and sham in a counterbalanced randomized order. There will be at least 3 days between each experimental session.

干预措施: transcranial direct current stimulation (Device)

transcranial direct current stimulation - tDCS sham

Placebo Comparator

tDCS will be applied over the motor cortex for 20minutes at an intensity of 2mA. The stimulation will be stopped after 30seconds.

15 subjects will be enrolled. The subjects will undergo two interventions, real and sham in a counterbalanced randomized order. There will be at least 3 days between each experimental session.

干预措施: transcranial direct current stimulation (Device)

结局指标

主要结局

Change in Motor Cortex Excitability MEP Amplitude

时间窗: after each intervention

We aim to assess the effects of the intervention (ML, SL, OT and MI) on motor cortex excitability as measured by the change in motor evoked potential (using transcranial magnetic stimulation) before and after the given intervention. * For ML: MEP will be measured before and after each ML sessions in the same subject (crossover design - ML sighted/MLblind/ML control). * For SL: MEP will be measured before and after the treatment session in the each groups (parallel design - 1 session per group). * For OT: MEP will be measured before and after the treatment session in the each groups (parallel - 1 session per group). * For MI: MEP will be measured before and after the treatment session in the each groups (parallel design - 1 session per group).

次要结局

未报告次要终点

研究者

发起方
Spaulding Rehabilitation Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Felipe Fregni

Principal Investigator

Spaulding Rehabilitation Hospital

研究点 (1)

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