None listed
Conditions
Interventions
Medical Device : For patients with traumatic brain injury, TDCS was applied to the left pre-frontal region 5 times a week, 2 weeks, 20 minutes each time, followed by FNIRS evaluation and clinical func
Sponsors
Eulji University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patient with traumatic brain injury confirmed using brain CT (computed tomography) or MRI (magnetic resonance imaging) who visited Eulji university hospital (inpatient/ outpatient) ? Subjects who have passed more than 1 month after the onset ? Those who have cognitive function to perform simple instructions and perform them ? Those who are 18 years of age or older and do not fall under the exclusion criteria ? Subject who voluntarily agreed to the clinical trial and agreed to the subject consent
Exclusion criteria
Exclusion criteria: ? Subjects with intellectual disabilities that are unable to carry out instructions that are not applicable to clinical evaluation ? Those who have a history of epileptic seizures ? Those who have undergone deep electric stimulation (DBS) in the cranial cavity or have an artificial pacemaker ? Subjects judged to be unsuitable for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Korean Montreal Cognitive Assessment; K-MoCA | — |
Secondary
| Measure | Time frame |
|---|---|
| Executive Clock Drawing Test; ECDT;Trail Making Test; TMT;Rey Complex Figure Test; RCFT | — |
Countries
Korea, Republic of
Contacts
Public ContactKang Jae Jung
Eulji University Hospital
Outcome results
None listed