Actively Recruiting

Phase Not Applicable
Age: 18Years - 89Years
All Genders
NCT07411859

Reboot Pain (tDCS)

Led by Emory University · Updated on 2026-04-14

100

Participants Needed

1

Research Sites

62 weeks

Total Duration

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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

Age: 18Years - 89Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

The Emory Clinic

Atlanta, Georgia, United States, 30308

Actively Recruiting

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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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