None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Pediatric patients between 6 and 23 years old (2) Patients that weigh over 25 kg (3) Patients diagnosed with ADHD as per DSM-IV diagnostic criteria or patients diagnosed with ADHD along with coexisting diseases (4) Patients taking Methylphenidate or Atomoxetine (5) IQ 70 or higher (6) Patients who have been thoroughly informed of the details of the study by the researcher/person delegated by the research director and have consented for study participation by the patient and the patient’s guardian.
Exclusion criteria
Exclusion criteria: (1) Patients that did not agree to participate in the study (2) IQ less than 70 (3) Patients with congenital genetic disease, cerebral palsy, or those with a clear history of acquired brain damage (4) Patients diagnosed with a seizure disorder or other neurological disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Resting-State Functional Magnetic Resonance Imaging (rs-fMRI);ADHD Rating Scale (ARS);Beck Depression Inventory (BDI);Barratt Impulsiveness Scale (BIS);Comprehensive Attention Test (CAT);Computerized NeuroCognitive Function test (CNT) | — |
Secondary
| Measure | Time frame |
|---|---|
| Korean Wechsler Adult Intelligence Scale (K-WAIS);Korean Wechsler Scale for Children (K-WISC) | — |
Countries
Korea, Republic of
Contacts
Chung-Ang University