Reboot Pain (tDCS)

NCT ID
NCT07411859
Registry status
Recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Emory University
Conditions
Chronic Pain

Overview

ClinicalTrials.gov lists this study as Recruiting.

Official title: Reboot Pain: Integrating Neuromodulation Into Clinical Care for Military and Veterans With Chronic Pain

Enrollment: 100 participants (Estimated).

What is being studied

  • Intervention: Behavioral Disciplines and Activities
  • Intervention: Convulsive Therapy
  • Intervention: Electric Stimulation Therapy
  • Intervention: Electroshock
  • Intervention: Psychiatric Somatic Therapies
  • Intervention: Psychological Techniques
  • Intervention: Therapeutics
  • Intervention: Transcranial Direct Current Stimulation
  • Device: Transcranial Direct Current Stimulation

Who may be eligible

Ages
18 Years to 89 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Male or Female, 18-89 years old * Treated on site for ABHP * Willing to self-administer tDCS and complete the measures * PEG 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 Criteria: * 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

Study locations

1 study location is listed.

Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.

Countries: United States

  • Georgia, United States: 1

Sample of listed locations

  • The Emory Clinic — Atlanta, Georgia, 30308, United States — Recruiting

Study details

Start date
February 16, 2026
Primary completion date
May 1, 2027
Completion date
May 1, 2027
First posted
February 17, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07411859
Registry last updated
April 14, 2026
QualifiedStudies registry data refreshed
October 2, 2026
QualifiedStudies record fetched
October 2, 2026

View NCT07411859 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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