Targeting Neuroplasticity for Persistent Post-Concussive Cognitive Symptoms
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Minnesota
About this trial
This project investigates an innovative combination of non-invasive neuromodulation (transcranial direct current stimulation - tDCS) and cognitive training as a novel treatment approach aimed at improving function in individuals suffering from persistent post-concussive syndrome (PPCS) following mild traumatic brain injury (mTBI).
Eligibility criteria
Qualifiers
Age 18-65
Has sustained a single mTBI 3-12 months prior to enrollment
Meets criteria for PPCS (assessed using the CP Screen)
Has reliable access to a smartphone
Disqualifiers
Inability to provide informed consent or complete study procedures
History of moderate/severe TBI
Significant neurological or psychiatric disorders (other than PPCS-related symptoms like mild depression/anxiety)
Substance dependence within the last six months
Trial design
Treatments tested in this trial
- Active tDCS
- Sham tDCS
Treatment groups
30 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov