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Clinical Trial Summary

Investigators are seeking to determine the effects of CBT, anodal tDCS over left DLPFC, and combined CBT+ tDCS on clinical pain and functioning among a sample of patients with fibromyalgia. This study will be the first randomized, double-blind, controlled study of tDCS technology as an adjunctive pain management strategy for fibromyalgia pain. Data from this trial will likely yield information regarding the feasibility and efficacy of tDCS+CBT as a chronic pain-management approach.


Clinical Trial Description

Patients with fibromyalgia will complete questionnaires, six cognitive behavioral therapy sessions, quantitative sensory testing before and after the six therapy sessions, and undergo 30 minutes of tDCS during each of the six therapy sessions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02723175
Study type Interventional
Source Medical University of South Carolina
Contact
Status Completed
Phase N/A
Start date December 2014
Completion date September 2017

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