Skip to main content
Clinical Trials/NCT01677819
NCT01677819
Completed
Not Applicable

Inhibition Control of Children and Adolescents With Attention-Deficit/Hyperactivity Disorder

National Taiwan University Hospital1 site in 1 country60 target enrollmentNovember 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Attention Deficit Hyperactivity Disorder
Sponsor
National Taiwan University Hospital
Enrollment
60
Locations
1
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The objectives of this study are to investigate:

  1. the effect of methylphenidate on attention;
  2. the relations between methylphenidate and inhibition control and working memory;
  3. the relations between inhibition control and verbal attention and working memory;
  4. the effect of methylphenidate on the changes of neuropsychological functioning and blood pressure.

Detailed Description

Attention deficit hyperactivity disorder (ADHD), characterized by inattention, hyperactivity and impulsivity, is an early onset, highly heritable, clinically heterogeneous, long-term impairing disorder with tremendous impact on individuals, families, and societies. It affects 5-10% of school-aged children worldwide (7.5% in Taiwan). Methylphenidate, a stimulant, is effective in treating these patients. Studies in Taiwan show no effect of methylphenidate on blood pressure. There are evidences show that the change of blood pressure was associated with inhibition of impulsive behaviors. Stop Signal Task(SST) is used to assess the improve of inhibition control after methylphenidate response. By using repeated outcome measurements, we anticipate that this study will evaluate the improvement of neuropsychological performances after medication and determinie the association between medication response and neuropsychological functions and vital signs in a Taiwanese sample.

Registry
clinicaltrials.gov
Start Date
November 2011
End Date
March 2012
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

National Taiwan University Hospital

Susan Shur-Fen Gau

National Taiwan University Hospital

Eligibility Criteria

Inclusion Criteria

  • The inclusion criteria for the subjects are (1)that subjects have a clinical diagnosis of ADHD defined by the DSM-IV which was made by a full-time board-certificated child psychiatrist; (2)their ages range from 10 to 18 when we conduct the study; (3)their IQ greater than 80; and (4)they are under treatment of methylphenidate.

Exclusion Criteria

  • The subjects will be excluded from the study if they currently meet criteria or have a history of the following condition as defined by DSM-IV: Schizophrenia, Schizoaffective Disorder, Organic Psychosis, or Pervasive Developmental Disorder.

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

Loading locations...

Similar Trials