Actively Recruiting
Reboot Pain (tDCS)
Led by Emory University · Updated on 2026-04-14
100
Participants Needed
1
Research Sites
62 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study will examine the effectiveness of tDCS (Transcranial Direct Current Stimulation) in reducing chronic pain when used with Emory Healthcare Veterans Program (EHVP)-ABHP (Accelerated Behavioral Health Program) participants as measured by the Pain, Enjoyment of Life and General Activity Scale (PEG).
CONDITIONS
Official Title
Reboot Pain (tDCS)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or Female, 18-89 years old
- Currently treated on site for Accelerated Behavioral Health Program (ABHP)
- Willing to self-administer tDCS and complete study measures
- Experience PEG pain intensity of 4 or more most of the day at least 3 days per week
- Have an established primary care provider or pain management provider
You will not qualify if you...
- Have an implanted pacemaker
- Have a seizure disorder
- Are pregnant
- Have new onset of balance problems, difficulty walking, bladder or bowel incontinence, numbness, tingling, or weakness
- Have medical contraindications including current use of sodium channel blockers, certain antidepressants, anti-epileptic medications, calcium channel blockers, NMDA receptor antagonists, ketamine, dextromethorphan, or felbamate
- History of brain surgery, brain tumor, stroke, seizure disorder, or intracranial metal implants
- Unable to provide consent
- Are prisoners
- Are non-English speaking
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Emory Clinic
Atlanta, Georgia, United States, 30308
Actively Recruiting
Research Team
S
Syreese Fuller
CONTACT
S
Sheila Rauch, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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