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Explore the Association Between Neuropsychological Functions and ADHD Diagnosis and Comorbid Using Longitudinal Study in Preschool Children

Explore the Association Between Neuropsychological Functions and ADHD Diagnosis and Comorbid Using Longitudinal Study in Preschool Children

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02433145
Enrollment
220
Registered
2015-05-04
Start date
2014-10-31
Completion date
2017-08-31
Last updated
2015-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit/Hyperactivity Disorder

Keywords

ADHD in preschoolers, neuropsychological functions, behavior inhibition, family function and parenting

Brief summary

The current study using the longitudinal study in preschool children to exam three study issues: 1) using the neuropsychological functions (ie. Behavioral inhibition, delay aversion, the variability of reaction time) among the preschool children predict the ADHD diagnosis and behavior symptoms in 1.5 years later. 2) using the behavior inhibition, delay aversion and the variability of reaction time (using the parameter among Gaussian distribution and ex-Gaussian distribution) explore the association between attention and motor inhibition problems. 3) explore the transaction effect between the neuropsychological functions and family function and parenting to predict ADHD comorbidity with oppositional defiant disorder.4) explore the association between the internalizing/ externalizing problems of ADHD and temperament. The current study has opportunity to describe and to answer the complicated problems for heterogeneous neuropsychological deficits in ADHD, and to elucidate the core issues for ADHD have comorbid with ODD. The most important contribution is to offer the empirical evidence to make a clean suggestion in ADHD diagnosis and intervention in preschool age.

Detailed description

The current study would follow the same participants for 1.5 years, time 1 is around 4-5 years old, and time 2 is around 6-7 years old. Participants: * 100 typical developmental control * 120 ADHD high risk preschool children at time 1 The diagnosis at time 2 to have three groups in this study: * ADHD persistent * ADHD remission * typical developmental control The measurements were included * the different neuropsychological test (ie. behavioral inhibition, delay aversion, and vigilance task) * the ADHD behavioral rating scales and diagnosis interview * the scaling for family function and parenting * intellectual assessment This study could offer the suggestion for the further intervention in ADHD.

Interventions

None listed

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
4 Years to 5 Years
Healthy volunteers
Yes

Inclusion criteria

1. Control group * The subjects without ADHD. * Ages range from 4 to 5 * Full scale IQ ≥ 80 * The subjects who and whose parents consent to this study. 2. ADHD high risk group * Patients who have clinically diagnosis of DSM-IV ADHD confirmed by the Psychiatrists or have the risk of becoming ADHD confirmed by the ADHD behavioral rating scales. * Ages range from 4 to 5 * Full scale IQ ≥ 80 * Patients who and whose parents consent to this study.

Exclusion criteria

* Mental Retardation * Schizophrenia, Schizoaffective Disorder * Mood Disorders * Organic Psychosis * Learning Disorder * Pervasive Developmental Disorder * The subjects of control group if have a history of the following condition as defined by DSM-IV: ADHD in addition to the above

Design outcomes

Primary

MeasureTime frame
The error rate and hit reaction time in the judgements on color flanker response inhibition test which measured by the e-prime program on the laptopup to 3 years

Secondary

MeasureTime frame
The error rate and hit reaction time in the day-night stroop test which measured by the e-prime program on the laptopup to 3 years

Other

MeasureTime frame
The final balloon numbers and eaction time in delay aversion test which measured by the e-prime program on the laptopup to 3 years

Countries

Taiwan

Contacts

Primary ContactSusan Shur-Fen Gau, MD, PhD
gaushufe@ntu.edu.tw02-23123456

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026