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临床试验/NCT03030794
NCT03030794已完成不适用

Alleviating Headache and Pain in GWI With Neuronavigation Guided rTMS

Veterans Medical Research Foundation2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2016年12月1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
发起方
入组人数
90
试验地点
2
主要终点
Daily Headache and Pain Log

研究概览

简要总结

This study aims to assess the effect of repetitive transcranial magnetic stimulation (rTMS) on Gulf War illness related headaches and pain.

详细描述

Headaches (HA) and wide spread pain are some of the most common debilitating symptoms in Gulf War Veterans (GWV) with Gulf War Illness (GWI). Migraine like HA and diffuse body pain were detected in 64% of GWV with GWI. This high prevalence of chronic HA and diffuse body pain conditions are often associated with neuropsychological dysfunction in mood, attention, memory and other systemic symptoms, which cast a profound negative impact on patients' quality of life. Unfortunately, conventional pharmacological treatments for GWI related headaches and pain (GWI-HAP) has not been shown to be effective and drugs such as narcotics contain many long term untoward psychosomatic and abusive side effects. Therefore, developing and validating non-invasive and low risk innovative treatment for this patient population is warranted. Transcranial Magnetic Stimulation (TMS) is currently a US FDA approved treatment for major depression and migraine HA.

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

入选标准

  • •Criteria for veterans with Gulf War Illness headaches and pain:
  • •Inclusion Criteria:
  • •Male or female between ages 18-65
  • •CDC Criteria for GWI
  • •Kansas Criteria for GWI
  • •International Headache Society Criteria for Migraine HA w/o aura
  • •Average Headache Exacerbation Intensity >3 on 0-10 NPRS
  • •Average Overall Daily Muscle Pain Intensity >3 on 0-10 NPRS
  • •Average Overall Daily Extremities Joint Pain Intensity >3 on 0-10 NPRS
  • •Headache Exacerbation/Attack ≥ 3 times/week, lasting >4 hrs in past 3 months

排除标准

  • •Pregnancy
  • •History of pacemaker implant
  • •Any ferromagnetic (e.g. bullet fragment, shrapnel, device implant) in the brain or body that will prohibit the patients from having a brain MRI
  • •History of dementia, major psychiatric diseases, or life threatening diseases
  • •Presence of any other chronic neuropathic pain states such as Complex Regional Pain Syndrome or Painful Peripheral Neuropathy
  • •History of seizure
  • •Pending litigation
  • •Low back pain with mechanical origins such as lumbar radiculopathy or radiculitis or lumbar facet arthropathy
  • •Lack of ability to understand the experimental protocol and to adequately communicate in English
  • •History of Traumatic Brain injury
  • •Chronic Tension or Cluster Headache
  • •Ongoing Cognitive Rehabilitation or Treatment of PTSD
  • •Criteria for healthy veterans without Gulf War Illness headaches and pain:
  • •Inclusion Criteria:
  • •Male or female between ages 18-65
  • •Served at least 30 consecutive days in the Persian Gulf between 8/90-7/91
  • •Exclusion Criteria:
  • •CDC Criteria for GWI
  • •Kansas Criteria for GWI
  • •International Headache Society Criteria for Migraine HA w/o aura
  • •Average Headache Exacerbation Intensity >3 on 0-10 NPRS
  • •Average Overall Daily Muscle Pain Intensity >3 on 0-10 NPRS
  • •Average Overall Daily Extremities Joint Pain Intensity >3 on 0-10 NPRS
  • •Headache Exacerbation/Attack ≥ 3 times/week, lasting >4 hrs in past 3 months
  • •Pregnancy
  • •History of pacemaker implant
  • •Any ferromagnetic (e.g. bullet fragment, shrapnel, device implant) in the brain or body that will prohibit the patients from having a brain MRI
  • •History of dementia, major psychiatric diseases, or life threatening diseases
  • •Presence of any other chronic neuropathic pain states such as Complex Regional Pain Syndrome or Painful Peripheral Neuropathy
  • •History of seizure
  • •Pending litigation
  • •Low back pain with mechanical origins such as lumbar radiculopathy or radiculitis or lumbar facet arthropathy
  • •Lack of ability to understand the experimental protocol and to adequately communicate in English
  • •History of Traumatic Brain injury
  • •Chronic Tension or Cluster Headache
  • •Ongoing Cognitive Rehabilitation or Treatment of PTSD

研究组 & 干预措施

Repetitive TMS

Active Comparator

Subjects will receive the repetitive transcranial magnetic stimulation study procedure.

干预措施: Repetitive transcranial magnetic stimulation (Device)

No (blocked) repetitive TMS

Placebo Comparator

Subjects will not receive the repetitive transcranial magnetic stimulation study procedure by blocking the stimulation between the coil and the head, but the audiovisual conditions will be mimicked.

干预措施: Repetitive transcranial magnetic stimulation (sham) (Device)

结局指标

主要结局

Daily Headache and Pain Log

时间窗: 2 months for each subject (11 visits)

This is a daily self-reporting log that tracks headache, muscle pain, and joint pain levels. The pain levels are scored from 0-10 with 10 being the worst possible pain.

Opioid Medication Assessment

时间窗: 2 months for each subject (11 visits)

This is a self-reporting log that tracks opioid medication usage. Average daily dosages are converted to equal-potent oral Morphine Sulfate dosage and reported in milligrams.

Headache Impact Test 6 (HIT-6)

时间窗: 2 months for each subject (11 visits)

This 6-question form assesses the severity of headache pain and is scored with a range of 36-78. The higher score, the higher the impact of headaches on functional ability.

2 months for each subject (11 visits)

时间窗: 2 months for each subject (11 visits)

This assessment has 9 questions about pain level, relief, and interference. Pain level and interference questions range from 0-10, with 10 being the worst. Level of relief has a range of 0-100%, with 100% being complete relief.

Mechanical-Visual Analogue Scale

时间窗: 2 months for each subject (11 visits)

This scale measures the level of headache, muscle, and joint pain at each visit. This ranges from 0-100, with 100 being the worst possible pain.

次要结局

  • Neurobehavioral Symptom Inventory (NSI)(2 months for each subject (11 visits))
  • Short-Form McGill Pain Questionnaire (SF-MPQ)(2 months for each subject (11 visits))
  • Hopkins Verbal Learning Test (HVLT)(2 months for each subject (11 visits))
  • This is a timed test that is administered to assess executive function. Both tests have a series of numbers or numbers and letters that are to be connected in sequential order. The faster the completion time, the better the executive function.(2 months for each subject (11 visits))
  • Hamilton Rating Scale for Depression(2 months for each subject (11 visits))
  • 36-Item Short Form Survey Instrument (SF-36)(2 months for each subject (11 visits))
  • Sleep Quality Assessment (PSQI)(2 months for each subject (11 visits))
  • New Clinical Fibromyalgia Diagnostic Criteria(2 months for each subject (11 visits))
  • Conners Continuous Performance Test 2 (CPT2)(2 months for each subject (11 visits))
  • Revised Fibromyalgia Impact Questionnaire (FIQR)(2 months for each subject (11 visits))
  • Trailmaking Test A&B(2 months for each subject (11 visits))
  • Insomnia Severity Index(2 months for each subject (11 visits))
  • Flinders Fatigue Scale(2 months for each subject (11 visits))

研究者

发起方
Veterans Medical Research Foundation
申办方类型
Other
责任方
Sponsor

研究点 (2)

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