Transcutaneous Auricular Vagus Nerve Stimulation for Persistent Post-concussion Symptoms

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Liege

About this trial

Persistent post-concussive symptoms (PPCS) affect a significant proportion of individuals following a concussion, leading to debilitating impacts on their quality of life and work capacity. Currently, effective treatments for PPCS are limited, despite their lasting and debilitating impact. Transcutaneous auricular vagus nerve stimulation (taVNS), a non-invasive neuromodulation technique, holds promise as a therapeutic option by leveraging the bottom-up modulation of brain activity via the auricular branch of the vagus nerve. This study aims to evaluate the neurophysiological and clinical effects of taVNS on brain activity and symptomatology in patients with PPCS through a randomized, controlled, double-blind trial.

Eligibility criteria

Qualifiers

Age between 18 and 65;

Between 4 weeks and 1-year post-diagnosis of a concussion;

Score equal or above 16 on the Rivermead Post-Concussion Questionnaire;

Intact skin at the electrode site.

Disqualifiers

History of chronic neurological or psychological disorders (still untreated 6 months preceding inclusion);

Pregnancy or breastfeeding;

Presence of an active implant (e.g., pacemaker, cochlear implant);

History of myocardial infarction or cardiac arrhythmia;

Trial design

Treatments tested in this trial

  • Active taVNS
  • Sham taVNS

Treatment groups

48 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Liege

Lead sponsor

University Hospital Sart Tilman, Liege

Collaborator