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Study identifier: NCT04199780 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effects of tDCS Combined With CBI on Postsurgical Pain

Condition: Total Knee Arthroplasty (Postoperative Pain) · Total Hip Arthroplasty (Postoperative Pain)  ·  Sponsor: VA Office of Research and Development

PhaseNA
Planned participants132
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

The purpose of this study is to determine whether a new medical technology can help reduce post-operative total knee or hip pain when combined with a Cognitive-Behavioral intervention (CBI). This new medical technology, is called transcranial direct current stimulation (tDCS), it uses a very small amount of electricity to temporarily stimulate specific areas of the brain thought to be involved in pain reduction. The electrical current passes through the skin, scalp, hair, and skull and requires no additional medication, sedation, or needles. This study will investigate the effects of tDCS, the Cognitive-Behavioral (CB) intervention and their combination on pain among veterans following total knee arthroplasty (TKA) or total hip arthroplasty (THA). The Veteran may benefit in the form of decreased pain and opioid requirements following knee or hip replacement surgery. However, benefit is only likely if Veterans are randomized to one of the 3 (out of 4) groups. This study hopes to determine the effects of these interventions and combined effect on post-operative pain, opioid use and functioning during the 48-hour post-operative period following a total knee or hip replacement.

This description comes directly from the study's public registry record.

Talk to the study team

Jeffrey J Borckardt, PhD  ·  (843) 577-5011  ·  Jeffrey.Borckardt@va.gov

Donald (Hugh) L Myrick, MD BS  ·  (843) 789-7316  ·  Donald.Myrick@va.gov

Always discuss trial participation with your own doctor first.

Locations (1)

Ralph H. Johnson VA Medical Center, Charleston, SCCharleston, South Carolina, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04199780