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临床试验/NCT04581525
NCT04581525终止不适用

Modulating Neuropathic Pain With Transcranial Direct Current Stimulation

Susan McDowell1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2012年6月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
发起方
入组人数
18
试验地点
1
主要终点
Change in McGill Pain Questionnaire from baseline 1 and 2 average

研究概览

简要总结

This study will examine whether a form of non-invasive brain stimulation can help reduce pain in people with persistent neuropathic pain.

详细描述

This study will look at the effects of a painless, non-invasive form of brain stimulation, called transcranial direct current stimulation, or tDCS. tDCS is thought to increase the brain's ability to change. Participants will be assigned to one of three groups by chance. Two groups will receive tDCS at a level expected to increase the brain's ability to change, while the other group will receive tDCS at a level not thought to affect the brain's ability to change.

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
Single (Participant)

入排标准

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

入选标准

  • •At least 18 years of age
  • •Have chronic (>12 months) neuropathic pain, including but not limited to complex regional pain syndrome, phantom limb pain, or pain of neurogenic origin following spinal cord injury

排除标准

  • •History of seizures or epilepsy
  • •Addition or change in the dosage of drugs now to interfere with pain within 1 month of enrollment
  • •Untreated depression
  • •History of head injury with loss of consciousness, severe alcohol or drug abuse, or psychiatric illness
  • •Positive pregnancy test or being of childbearing age and not using appropriate contraception
  • •Presence of ferromagnetic material in the cranium except in the mouth, including metal fragments from occupational exposure, and surgical clips in or near the brain

研究组 & 干预措施

tDCS of DLPFC

Experimental

Subjects will receive 20 minutes of active transcranial direct current stimulation at 2mA applied to the left dorsolateral prefrontal cortex (DLPFC). Subjects will undergo stimulation once a day for 10 consecutive weekdays.

干预措施: transcranial direct current stimulation (Device)

tDCS of M1

Experimental

Subjects will receive 20 minutes of active transcranial direct current stimulation at 2mA applied to the left primary motor cortex (M1). Subjects will undergo stimulation once a day for 10 consecutive weekdays.

干预措施: transcranial direct current stimulation (Device)

Sham tDCS

Sham Comparator

Subjects will receive 20 minutes of sham transcranial direct current stimulation. Subjects will undergo stimulation once a day for 10 consecutive weekdays.

干预措施: transcranial direct current stimulation (Device)

结局指标

主要结局

Change in McGill Pain Questionnaire from baseline 1 and 2 average

时间窗: Baseline 1: 1 week before starting intervention, Baseline 2: immediately before starting intervention, Intervention mid-point: after 5 days intervention, Post-intervention: after 10 days intervention, Follow up: 1 month after completing intervention

This self-reported assessment measures intensity and quality of pain. Scores can range from 0 to 45. A decrease in score indicates an improvement in pain.

次要结局

  • Change in Short-Form 36 Health Survey from baseline 1 and 2 average(Baseline 1: 1 week before starting intervention, Baseline 2: immediately before starting intervention, Intervention mid-point: after 5 days intervention, Post-intervention: after 10 days intervention, Follow up: 1 month after completing intervention)

研究者

发起方
Susan McDowell
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Susan McDowell

Associate Professor

University of Kentucky

研究点 (1)

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