Attention Control Training for PTSD in Children
Randomized Clinical Trial of Attention Control Training for Symptoms of PTSD in Children
1 other identifier
interventional
89
1 country
1
Brief Summary
Participants will complete a pre and post training psychological assessment. Participants will be assigned to attention control training or the comparison stimuli computer task in a double-blind randomized control trial design. Both computerized dot probe tasks display two faces on a computer screen, one above the other, followed by a small right or left arrow appearing in the location vacated by one of the faces. Participants are required to respond as quickly as they can by pressing the indicated right or left arrow on their computer keyboard without compromising accuracy. Participants complete 6 training sessions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2017
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 16, 2017
CompletedStudy Start
First participant enrolled
November 20, 2017
CompletedFirst Posted
Study publicly available on registry
November 21, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 20, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
November 20, 2023
CompletedFebruary 8, 2024
February 1, 2024
6 years
November 16, 2017
February 6, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test
PTSD self-report questionnaire
10 minute long administration, given twice to measure change scores from pre and post training approximately 1 month apart
Study Arms (2)
Attention Control Training
EXPERIMENTAL* 6 sessions in the clinic lasting approximately 10 minutes each. * Each session will consist of 128 presentations of pairs of neutral and threatening stimuli, followed by the presentation of a response cue (right or left arrow to be clicked on a computer keyboard).
Comparison Task
PLACEBO COMPARATOR6 sessions in the clinic of a presumably inactive neutral-neutral stimuli intervention lasting approximately 10 minutes each. • Each session will consist of 128 presentations of pairs of faces, followed by the presentation of a response cue (right or left arrow to be clicked on a computer keyboard).
Interventions
Attention control training teaches participants that the emotional salience of cues (i.e., threatening or neutral) is not related to successful completion of the computerized response task, and thus, teaches participants to ignore irrelevant threat-related contingencies (Badura-Brack et al., 2015).
Eligibility Criteria
You may qualify if:
- significant symptoms of PTSD and qualifying traumatic event
You may not qualify if:
- new traumatic event within one month of beginning the trial
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Creighton Univeristy
Omaha, Nebraska, 68178, United States
Related Publications (1)
Badura-Brack AS, Naim R, Ryan TJ, Levy O, Abend R, Khanna MM, McDermott TJ, Pine DS, Bar-Haim Y. Effect of Attention Training on Attention Bias Variability and PTSD Symptoms: Randomized Controlled Trials in Israeli and U.S. Combat Veterans. Am J Psychiatry. 2015 Dec;172(12):1233-41. doi: 10.1176/appi.ajp.2015.14121578. Epub 2015 Jul 24.
PMID: 26206075BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Psychology
Study Record Dates
First Submitted
November 16, 2017
First Posted
November 21, 2017
Study Start
November 20, 2017
Primary Completion
November 20, 2023
Study Completion
November 20, 2023
Last Updated
February 8, 2024
Record last verified: 2024-02