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NCT03932032 · ClinicalTrials.gov registry record · NA
Targeting Attention Orienting to Social Threat to Reduce Social Anxiety in Youth
A NA study of Social Anxiety Disorder of Childhood, sponsored by Florida International University.
- Active
- Registry status
- NA
- Development phase
- 260
- Enrollment target
- 2
- Study locations
NCT03932032 is a NA study of Social Anxiety Disorder of Childhood that is active but no longer recruiting, run by Florida International University. The registered enrollment target is 260 participants. The trial reports 2 study locations across 2 states.
The verdict
NCT03932032, a NA study of Social Anxiety Disorder of Childhood, is active but no longer recruiting, sponsored by Florida International University.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 260 participants
- Enrollment target
- 2
- Study locations
Study Summary
This two-site study is a test of Attention Bias Modification Treatment (ABMT) among 260 youths ages 10 to 14 years with social anxiety disorder. One-half of participants will receive 8 sessions of computer administered ABMT and the other half of participants will receive 8 sessions of computer administered Neutral Control Task (NCT). The investigators hypothesize that a biomarker of attention to social threat measured using electroencephalography (EEG) and ratings of social anxiety severity will be lower in participants who receive ABMT compared to participants who receive NCT.
Conditions Studied
Interventions
- BEHAVIORAL Attention Bias Modification Treatment
- BEHAVIORAL Neutral Control Task
Study Locations (2)
Connecticut
- Yale Child Study Center Program for Anxiety and Mood Disorders - New Haven
Florida
- Florida International University Center for Children and Families - Miami
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 260 participants |
| Start Date | 2019-07-01 |
| Est. Completion | 2026-03-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03932032
The ClinicalTrials.gov registry entry for NCT03932032 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 260 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Florida International University, which has 89 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Social Anxiety Disorder of Childhood appearing as the primary indexed condition, and to 2 interventions - of which Attention Bias Modification Treatment is the first listed.
NCT03932032 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Connecticut, Florida.
Frequently Asked Questions
What is clinical trial NCT03932032 about?
NCT03932032 is a clinical study titled "Targeting Attention Orienting to Social Threat to Reduce Social Anxiety in Youth". This two-site study is a test of Attention Bias Modification Treatment (ABMT) among 260 youths ages 10 to 14 years with social anxiety disorder. One-half of participants will receive 8 sessions of computer administered ABMT and the other half of participants will receive 8 sessions of computer admin...
What is the current status of trial NCT03932032?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 260 participants. The study started on 2019-07-01. Estimated completion is 2026-03-31.
What conditions does trial NCT03932032 study?
This clinical trial studies the following conditions: Social Anxiety Disorder of Childhood.
What interventions are being tested in trial NCT03932032?
The interventions under investigation include: Attention Bias Modification Treatment (BEHAVIORAL), Neutral Control Task (BEHAVIORAL).
Who is sponsoring clinical trial NCT03932032?
This trial is sponsored by Florida International University, which has 89 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03932032 being conducted?
This trial has 2 study locations across Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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