NCT02443051

Brief Summary

This research is designed to determine the effectiveness of attention bias modification for socially anxious children and adolescents. Over the course of 3 years, 50 youth will be enrolled in the trial.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2013

Longer than P75 for not_applicable

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2013

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

May 2, 2015

Completed
11 days until next milestone

First Posted

Study publicly available on registry

May 13, 2015

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2016

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
Last Updated

May 16, 2017

Status Verified

May 1, 2017

Enrollment Period

3 years

First QC Date

May 2, 2015

Last Update Submit

May 12, 2017

Conditions

Social Anxiety Disorder

Outcome Measures

Primary Outcomes (1)

  • Clinician Severity Rating

    Immediately following treatment

    Post-treatment

Study Arms (2)

Attention Bias Modification

EXPERIMENTAL

Training in bias modification for 80% of experimental trials

Behavioral: Attention Bias Modification

Control

ACTIVE COMPARATOR

Bias modification for 50% of trials

Behavioral: Attention Bias Modification

Interventions

Attention Bias ModificationBEHAVIORAL

Computer delivered modification in 80% of trials

Attention Bias ModificationControl

Eligibility Criteria

Age11 Years - 16 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Diagnosis of Social Anxiety Disorder;
  • English Speaking

You may not qualify if:

  • Suicide Intent,
  • Psychosis,
  • Autism Spectrum Disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Child Study Center

Blacksburg, Virginia, 24060, United States

Location

MeSH Terms

Conditions

Phobia, Social

Condition Hierarchy (Ancestors)

Phobic DisordersAnxiety DisordersMental Disorders

Study Officials

  • Thomas H. Ollendick, Ph.D.

    Virginia Polytechnic Institute and State University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor - Principal Investigator

Study Record Dates

First Submitted

May 2, 2015

First Posted

May 13, 2015

Study Start

May 1, 2013

Primary Completion

May 1, 2016

Study Completion

December 1, 2016

Last Updated

May 16, 2017

Record last verified: 2017-05

Locations

US(1)