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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03725371
Other study ID # YNC-SASSI-Quanti-1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2011
Est. completion date August 2015

Study information

Verified date October 2018
Source Yale-NUS College
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study investigates the psychophysiological correlations of aggression and response to aversive stimuli in a population of 133 children clinically diagnosed with conduct disorder (CD) and/or attention-deficit/hyperactivity disorder (ADHD). Data was gathered about participants' level of aggression through the Reactive-Proactive Aggression Questionnaire (RPQ). The stimuli that were presented to the participants included 1) a loud sound, 2) threatening photographs from the International Affective Picture System (IAPS), and 3) the Trier Social Stress Task (TSST). Participants' psychophysiological features of heart rate and galvanic skin conductance were measured and analyzed in relation to their RPQ scores and clinical diagnosis.


Recruitment information / eligibility

Status Completed
Enrollment 133
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender All
Age group 7 Years to 16 Years
Eligibility Inclusion Criteria:

1. Subjects between ages 7 and 16 years

2. Subjects who fulfil all criteria for a DSM-IV diagnosis of ADHD, conduct disorder, or oppositional defiant disorder

3. Subjects with willingness to participate in a randomized, double-blind controlled trial

4. Subjects with complete written, informed parental consent and child assent

5. Subjects with IQ of 70 or more

Exclusion Criteria:

1. Subjects who have IQ in the below 70

2. Subjects who are younger than 7 years old or older than 16 years old

3. Those without written parental consent

4. Those with brain pathology such as serious head injury, epilepsy, etc.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention was administered for the purpose of this study.
No intervention was administered for the purpose of this study. Observations were carried out for all participants.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yale-NUS College

Outcome

Type Measure Description Time frame Safety issue
Primary Heart Rate For Trier Social Stress Task 7 minutes
Primary Skin Conductance Response For loud sound 4 minutes
Primary Skin Conductance Response For threatening photograph 4 minutes
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