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Clinical Trials/NCT01397032
NCT01397032
Completed
Phase 2

Attention Bias Modification Treatment for Children With Social Anxiety

Tel Aviv University1 site in 1 country67 target enrollmentApril 2011
ConditionsSocial Phobia

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Social Phobia
Sponsor
Tel Aviv University
Enrollment
67
Locations
1
Primary Endpoint
Anxiety Disorders Interview Schedule for DSM-IV (ADIS)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Children with social anxiety will be randomly assigned to either Attention Bias Modification Treatment (ABMT) designed to direct attention away from threat or a placebo control condition not designed to change attention patterns. Outcome measures will be depression and social anxiety symptoms as measured by gold standard questionnaires as well as diagnosis of social phobia disorder and symptom counts derived from structured clinical interviews with children and their parents.

We expect to see significant reduction in social anxiety symptoms in the Attention Bias Modification Treatment (ABMT) group relative to the placebo control group.

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
August 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yair Bar-Haim

Head of Shcool of Psychological Sciences, Tel-Aviv University

Tel Aviv University

Eligibility Criteria

Inclusion Criteria

  • children suffering from social anxiety

Exclusion Criteria

  • Pharmacological or Psychological treatment

Outcomes

Primary Outcomes

Anxiety Disorders Interview Schedule for DSM-IV (ADIS)

Time Frame: expected average time frame of 6 weeks. Participants will be assessed before and after the administriation of the training/control protocols.

The ADIS is a semi-structured interview assessing anxiety, mood and externalizing disorders in children according to DSM-IV criteria.

Secondary Outcomes

  • Social Phobia and Anxiety Inventory for Children (SPAI-C) and for Parents (SPAI-c-p)(expected average time frame of 6 weeks. Participants will be assessed before and after the administriation of the training/control protocols.)

Study Sites (1)

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