Status:

COMPLETED

Transcranial Direct Current Stimulation Treatment for Warriors Experiencing Chronic Pain

Lead Sponsor:

Emory University

Collaborating Sponsors:

Wounded Warrior Project

Conditions:

Chronic Pain

Post Traumatic Stress Disorder (PTSD)

Eligibility:

All Genders

18-89 years

Phase:

NA

Brief Summary

The Veteran population has been known to deal with co-morbid chronic pain and PTSD. As a result, they use healthcare services at a higher rate than those Veterans with pain or PTSD alone which leads t...

Detailed Description

The Veteran population has been known to deal with co-morbid chronic pain and PTSD. As a result, they use healthcare services at a higher rate than those Veterans with pain or PTSD alone which leads t...

Eligibility Criteria

Inclusion

  • Male or Female, 18 -89 years old
  • Treated on site for EHVP IOP
  • For long-term follow-up, must live in Georgia or Florida
  • Eligible for EHVP-IOP PTSD or Unified Protocol tracks
  • Willing to self-administer tDCS and complete the measures
  • DVPRS pain intensity of 4 or more for most of the day at least 3 days per week
  • Have an established PCP (Primary Care Provider) or pain management provider

Exclusion

  • Implanted pacemaker
  • Seizure Disorder
  • Pregnancy, if applicable
  • Any new onset of the following:
  • Balance problems
  • Difficulty walking
  • Bladder incontinence
  • Bowel incontinence
  • Numbness
  • Tingling
  • Weakness
  • Medical contraindications:
  • Current use of sodium channel blockers
  • Lidocaine (OTC/transdermal delivery is ok)
  • Mexiletine
  • Amitriptyline; other tricyclic antidepressants
  • Anti-epileptic medications
  • Phenytoin, carbamazepine, lamotrigine, oxcarbazepine, rufinamide, lacosamide and eslicarbazepine acetate
  • Current use of calcium channel blockers
  • Current use of N-Methyl-D-aspartate receptor antagonists
  • Ketamine
  • Dextromethorphan
  • Felbamate
  • History of brain surgery
  • History of brain tumor
  • History of seizure disorder
  • History of stroke
  • Intracranial metal implantation
  • Adults unable to consent
  • Individuals who are not yet adults
  • Prisoners
  • Non-English speaking

Key Trial Info

Start Date :

March 4 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 31 2025

Estimated Enrollment :

38 Patients enrolled

Trial Details

Trial ID

NCT05254379

Start Date

March 4 2022

End Date

May 31 2025

Last Update

September 11 2025

Active Locations (1)

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1

Emory Division of Psychiatry

Atlanta, Georgia, United States, 30329