rTMS in Alleviating Pain and Co-Morbid Symptoms in Gulf War Veterans Illness (GWVI)

a study on Gulf War Syndrome Depression Transcranial Magnetic Stimulation

Summary

Eligibility
for people ages 18-65 (full criteria)
Location
at UCSD
Dates
study started
completion around
Principal Investigator
by Albert Yick Leung, MD (ucsd)
Headshot of Albert Yick Leung
Albert Yick Leung

Description

Summary

This study aims to look at the effectiveness of using repetitive transcranial magnetic stimulation (rTMS) in relieving pain and other co-morbid symptoms of Gulf War Illness.

Official Title

rTMS in Alleviating Pain and Co-morbid Symptoms in GWVI

Details

Headaches (HA), muscle and joint pain, are some of the most common debilitating symptoms in military personnel served in the 1990-1991 Persian Gulf War (GW1). Migraine like HA and diffuse body pain were detected in 64% of Gulf War Veteran (GWV) diagnosed with Gulf War Illness (GWI). Likewise, depression carries a very high co-morbid rate (50%) in patients with chronic pain, and in GWV with GWI related chronic HA and body muscle and joint pain conditions (GWI-HAP). Unfortunately, conventional pharmacological treatments for GWI-related pain has not been shown to be effective and drugs such as narcotics contain many long term untoward psychosomatic and abusive side effects. This study is assessing the effectiveness of repetitive transcranial magnetic stimulation (rTMS), non-invasive treatment option, in alleviating pain and other co-morbid symptoms of GWI.

Keywords

Gulf War Illness, Depression, rTMS, Transcranial Magnetic Stimulation

Eligibility

You can join if…

Open to people ages 18-65

  • Male or female under 65 years of age who served in the military for at least 30 consecutive days between August 1, 1990, and July 31, 1991 in the Persian Gulf War region
  • CDC Criteria for GWVI (GWI)
  • Kansas Criteria for GWVI (GWI)
  • International Headache Society Criteria for Migraine Headache without aura
  • Average Overall Daily Muscle Pain Intensity >3 on 0-10 a NPS
  • Average Overall Daily Extremities Joint Pain Intensity >3 on 0-10 a NPS
  • Headache Exacerbation/attack once a week with the average intensity >3 on a 0-10 NPS, lasting > 1 hour in the past three months
  • Hamilton Rating Scale of Depression (HRSD) greater than or equal to 14 based on the sum of scores for the first 17 items

You CAN'T join if...

  • 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

Locations

  • VA San Diego Healthcare System, San Diego, CA accepting new patients
    San Diego California 92161-0002 United States
  • VA Palo Alto Health Care System, Palo Alto, CA accepting new patients
    Palo Alto California 94304-1290 United States
  • Atlanta VA Medical and Rehab Center, Decatur, GA accepting new patients
    Decatur Georgia 30033 United States

Lead Scientist at University of California Health

  • Albert Yick Leung, MD (ucsd)
    Clinical Professor, Anesthesiology, Vc-health Sciences-schools. Authored (or co-authored) 35 research publications. Research interests: Neuromodulation · Non-invasive Neuromodulation · Transcranial Magnetic Stimulation · Transcutaneous Magnetic Stimulation · Post-traumatic Brain Injury Headache · Non-pharmacological Treatment for Headaches · Neuropathic Pain · Trigeminal Neuralgia

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
VA Office of Research and Development
ID
NCT04046536
Study Type
Interventional
Participants
Expecting 80 study participants
Last Updated