Explore the Association Between the Emotion Recognition and the Attention Processing Under the Emotional Stimuli in ADHD

December 16, 2013 updated by: National Taiwan University Hospital
Lots of studies suggest that children with ADHD have deficits in facial emotion recognition, especially for the negative emotion. But there were arguments for this deficit is a secondary problem due to the general attention impairment in ADHD, or a specific social cognitive processing to ADHD. The objectives of this study are to investigate that association between the deficits in facial emotion recognition and the emotional attention processing in ADHD. In this study, the investigators use the emotion attentional bias and emotional go / no go paradigm to answer this question.

Study Overview

Status

Unknown

Detailed Description

The sample will consist of 100 children and adolescent with ADHD and 100 typical controls, ages 8-16. The ADHD group inclusion criteria are patients who have clinically diagnosis of DSM-IV ADHD confirmed by the K-SADS-E, and have IQ > 80; and whose parents consent to this study.

The measurements will be included:

  1. Diagnostic assessment tools:

    • Chinese version of Kiddie-Schedule for Affective Disorders and Schizophrenia-Epidemiology version.
    • Conners' Parent/Teacher Rating Scale- Revised: Short Form, CPRS-R:S/CTRS-R:S.
    • Swanson, Nolan, and Pelham, Version Ⅳ(SNAP-Ⅳ)Rating Scale - Parent/ Teacher Form.
  2. Emotion assessment tools:

    • Facial emotion recognition task.
    • Emotional attentional bias task.
    • Emotional Go/ No Go task.
  3. Cognitive assessment tool:

    • Wechsler Intelligence Scale for Children-Fourth Edition Chinese Version.

This study could offer the suggestion for the further intervention of social function in ADHD.

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan
        • Recruiting
        • National Taiwan Univeristy Hospital
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

4 years to 12 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

We will recruit 100 children and adolescent with ADHD and 100 typical controls.

Description

Inclusion Criteria:

  1. Control group

    • The subjects without ADHD.
    • Ages range from 8 to 16
    • Full scale IQ ≥ 80
    • The subjects who and whose parents consent to this study.
  2. ADHD group

    • Patients who have clinically diagnosis of DSM-IV ADHD confirmed by the K-SADS-E.
    • Ages range from 8 to 16
    • 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 exclusion criteria will be excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The error rate in facial emotion judgements on computerized task
Time Frame: up to 2 years
Investigator used the e-prime program to assess the error rate in facial emotion judgements. Participants need to judge the emotion of the face stimuli presented on the laptop.
up to 2 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The reaction time of attentional bias for pairs of face stimuli(happy/neutral or angry/neutral faces) on dot-prob task
Time Frame: up to 2 years
Investigator presented pairs of face stimuli with emotional and neutral expressions and probed the allocation of attention to these stimuli for presentation times of 150 and 500 ms to assess the reaction time of attentional bias. Participants need to press the dot after the prob.
up to 2 years

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
The attentional inhibition control(omission errors and commission errors) in emotional go/no go task
Time Frame: up to 2 years
Investigator used go/ no go task to assess participants' omission errors and commission errors, participants just need to press the keyboard and the number of errors were recorded.
up to 2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Susan Shur-Fen Gau, MD, PhD, National Taiwan University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2013

Primary Completion (Anticipated)

January 1, 2016

Study Completion (Anticipated)

January 1, 2016

Study Registration Dates

First Submitted

December 4, 2013

First Submitted That Met QC Criteria

December 16, 2013

First Posted (Estimate)

December 20, 2013

Study Record Updates

Last Update Posted (Estimate)

December 20, 2013

Last Update Submitted That Met QC Criteria

December 16, 2013

Last Verified

December 1, 2013

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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