CClinicalTrials.gg
CompletedNCT03171363Updated Sep 18, 2018

Gaze Contingent Feedback for Anxiety Disorders in Children

An interventional study of Gaze-contingent feedback in Anxiety Disorders, sponsored by Tel Aviv University. Completed at 1 site in Israel. Open to participants aged 6 Years to 10 Years. Per ClinicalTrials.gov, last updated 2018-09-18.

Sponsored by Tel Aviv University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Not applicable
Ages
6 Years to 10 Years
Sex
All
01

Study summary

The purpose of this study is to determine whether giving gaze-contingent feedback is an effective attention modification procedure, helping in the treatment of anxiety disorders in children.

Read the detailed description

Attention biases in threat processing have been assigned a prominent role in the etiology and maintenance of anxiety disorders. The purpose of this study is to determine whether giving gaze-contingent feedback is an effective treatment for anxiety disorders in clinically anxious 6-10 year-olds children. Participants will be assessed using clinical interviews and parent- and self-rated questionnaires before and after eight training sessions. Outcome measures will be anxiety symptoms and depression as measured by gold standard questionnaires as well as structured clinical interviews with children and their parents. Attentional threat bias and Attentional control will also be measured to explore potential mediators of ABMT's effect on anxiety.

02

Conditions studied

  • Anxiety Disorders

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Keywords

  • Attention bias modification treatment
  • Anxiety disorders
  • Attention training
03

In context

Anxiety Disorders

4,864 studies on the registry are indexed under Anxiety Disorders; 1,388 are open to participants now.

This study's enrollment of 12 is below the median of 80 across 4,170 interventional studies indexed under Anxiety Disorders.

Browse Anxiety Disorders studies →

Lead sponsor

Tel Aviv University is the lead sponsor of 100 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 10 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Primary diagnosis of GAD, SOP, or SAD.
  • Co-morbid attention deficit hyperactivity disorder (ADHD) or depressive disorders must be treated with medication and stable.
  • Tics or impulse control problems must be treated with medication, stable and cause minimal or no impairment.

Exclusion Criteria: To be excluded youth must:

  • meet diagnostic criteria for Organic Mental Disorders, Psychotic Disorders, Pervasive Developmental Disorders, or Mental Retardation.
  • show high likelihood of hurting themselves or others.
  • have not been living with a primary caregiver who is legally able to give consent for the child's participation.
  • be a victim of previously undisclosed abuse requiring investigation or ongoing supervision.
  • be involved currently in another psycho-social treatment.
  • have a serious vision problem that is not corrected with prescription lenses.
  • have a physical disability that interferes with their ability to click a mouse button rapidly and repeatedly.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
12 participants (actual)

Study arms

  • Experimental
    Gaze-contingent feedback

    Participants will receive gaze-contingent feedback according to their viewing patterns

    Behavioral: Gaze-contingent feedback

Interventions

  • BehavioralGaze-contingent feedback

    Participants will receive gaze-contingent feedback according to their viewing patterns

06

What researchers measure

Primary outcomes

  1. Change from baseline in anxiety symptoms - the Pediatric Anxiety Rating (PARS)

    The PARS assesses global anxiety severity across different anxiety disorders in children

    Time frame: Post treatment (1 week after treatment completion)

Secondary outcomes

  1. Change from baseline in anxiety related emotional disorders symptoms - Child/Parent (the SCARED 41-item)

    The SCARED is a 41-item self and parent-report instrument designed to assess anxiety in children.

    Time frame: Post treatment (1 week after treatment completion)

07

Study locations

1 site
  • Tel Aviv University
    Tel Aviv, 69978, Israel
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03171363
Lead sponsor
Tel Aviv University
Responsible party
Yair Bar-Haim (Professor of Psychology and Neuroscience School of Psychological Sciences Sagol School of Neuroscience Tel Aviv University, Tel Aviv University) — Principal investigator
First posted
May 31, 2017
Start date
Apr 1, 2017
Primary completion
Apr 1, 2018
Completion
Apr 1, 2018
Last update
Sep 18, 2018

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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