Stroke
Conditions
Brief summary
The primary objective of this study is to confirm and compare the effect of methods of transcranial direct current stimulation(tDCS) in the unilateral neglect of stroke patients
Detailed description
Total 105 patients were recruited and randomized to receive either real or sham-tDCS. Real experimental groups were divided into two types; Pre-tDCS group and Simultaneous tDCS group. Two groups are again divided into three groups; Dual stimulation group, Unilateral stimulation group and Sham control group, respectively. In Pre-tDCS group, total a sessions of the tDCS stimulation was done for each three subgroups and visual inattention training was followed after that. In Simultaneous tDCS group, tDCS and visual inattention training was done simultaneously. For each subgroups, tDCS was attached at following locations; unilateral cathodal tDCS on unaffected PPC(postparietal cortex), P3 , dual cathodal tDCS on P3 and anodal tDCS on affected PPC, P4. The patients were initially evaluated at baseline, immediately, 60min, 120min, 24 hrs after the training session.
Interventions
DEVICETranscranical direct current stimulator
approved by Conformity European as safe treatment device for stroke patients
BEHAVIORALVisual inattention training
Sponsors
Medwill hospital
Pusan National University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Subjects who have diagnosed as primary stroke by physician's physical exam or radiologic diagnosis * Subjects who have cortical or subcortical brain lesion * Subjects ages older than 18years old * Subjects who have 19 of K-MMSE score * Subjects who has unilateral neglect with BIT-C less than 129 * Subjects who understand the purpose of the study and acquired the consent of the patient or caregiver * Subjects who had no effect from brain stimulation or electrical stimulation therapy * Subjects whose dominant side are confirm by Edinburgh Handedness Inventory
Exclusion criteria
* Subjects who have pre-existing and active major neurological disease * Subjects who have pre-existing and active major psychiatric disease, such as major depression, schizophrenia, bipolar disease, or dementia * Subjects who have brain lesion except cortex or subcortex area * Subjects who have any metal component after brain surgery, low threshold to pain, history of seizure * Subjects who is estimated as not appropriate for the study by the investigators
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Behavioral Inattention Test | up to 2 min | Line bisection test |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Behavioral Inattention Test | 60 min, 120 min, 24 hrs after intervention | Line bisection test |
| ADL assssement | 60 min, 120 min, 24 hrs after intervention | Catherine Bergego Scale |
Countries
South Korea
Contacts
Primary ContactYong-Il Shin, Ph.D.
Outcome results
None listed