NCT02710929

Brief Summary

Specific Aims:

  1. 1.To find the genetic variations associated with spatial working memory performance in patients with ADHD by using genome-wide association studies (GWAS);
  2. 2.To find the genetic variations associated with spatial working memory performance in healthy subjects by using GWAS;
  3. 3.To recruit a validation sample and to replicate the findings from the initial GWAS;
  4. 4.To test whether genetic variations significantly associated with spatial working memory are also associated with ADHD.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
232

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2015

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2015

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

March 13, 2016

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 17, 2016

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2018

Completed
Last Updated

September 2, 2021

Status Verified

September 1, 2021

Enrollment Period

3 years

First QC Date

March 13, 2016

Last Update Submit

September 1, 2021

Conditions

Outcome Measures

Primary Outcomes (1)

  • Psychiatric interview

    Subjects will be interviewed by Chinese Version of the Kiddie Epidemiologic version of the Schedule for Affective Disorders and Schizophrenia (K-SADS-E)

    1 hour

Secondary Outcomes (1)

  • Spatial working memory

    30 minutes

Study Arms (2)

ADHD group

Subjects with clinical diagnosis of ADHD according to the DSM-IV criteria

TD group

Typically development controls without lifetime diagnosis with ADHD

Eligibility Criteria

Age7 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

The existing sample is composed of 382 children withADHD and 150 healthy subjects. We plan to recruit additional 232 healthy subjects (104 in the first year; 128 in the second year), aged 7 to 18 years.

You may qualify if:

  • Subjects without any current or lifetime DSM-IV psychiatric disorders based on the K-SADS-E interviews.

You may not qualify if:

  • Participants who had any past or current medical or neurological illness, who currently took psychotropic medication, or whose intelligence quotient (IQ) score was less than 80 were excluded.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan Univeristy Hospital

Taipei, Taiwan

Location

Biospecimen

Retention: SAMPLES WITH DNA

15 ml blood will be withdrawn from the subjects (one heparin-rinsed tube for cell culture, one EDTA rinsed tube for DNA extraction)

MeSH Terms

Conditions

Attention Deficit Disorder with Hyperactivity

Condition Hierarchy (Ancestors)

Attention Deficit and Disruptive Behavior DisordersNeurodevelopmental DisordersMental Disorders

Study Officials

  • Chi-Yung Shang, MD

    Dept of Psychiatry, National Taiwan University Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 13, 2016

First Posted

March 17, 2016

Study Start

August 1, 2015

Primary Completion

July 31, 2018

Study Completion

July 31, 2018

Last Updated

September 2, 2021

Record last verified: 2021-09

Data Sharing

IPD Sharing
Will not share

Locations