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Attention biases in threat processing have been assigned a prominent role in the etiology and maintenance of anxiety disorders. Attention Bias Modification Treatment (ABMT) utilizes computer-based protocols to implicitly modify biased attentional patterns in anxious patients. This is a double-blind randomized controlled trial of ABMT for clinically anxious 10-18 year-olds. Participants will be assessed using clinical interviews and parent- and self-rated questionnaires before, in the middle and after twelve sessions of ABMT or control groups, and again at ten-week follow-up. Outcome measures will be anxiety symptoms and depression as measured by gold standard questionnaires as well as structured clinical interviews with youth and their parents. Attentional threat bias, Attentional control and interpretation of ambiguous information will also be measured to explore potential mediators of ABMT's effect on anxiety. The investigators expect the findings to inform pathways to treatments for anxious children and to provide initial information on mechanisms of ABMT efficacy.
Age
10 - 18 years
Sex
ALL
Healthy Volunteers
No
Tel-Aviv University
Tel Aviv, Israel
Start Date
May 1, 2015
Primary Completion Date
May 1, 2018
Completion Date
May 1, 2018
Last Updated
September 18, 2018
100
ACTUAL participants
Attention Bias Modification treatment (ABMT)
BEHAVIORAL
Exposure only +ABMT
BEHAVIORAL
Attention training only +ABMT
BEHAVIORAL
Placebo group
BEHAVIORAL
Lead Sponsor
Tel Aviv University
NCT07432945
NCT06661460
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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View ClinicalTrials.gov Terms and ConditionsNCT07235852