MedPath

Attention Control Training for PTSD in Children

Not Applicable
Completed
Conditions
PTSD
Interventions
Behavioral: Comparison Task
Behavioral: Attention Control Training
Registration Number
NCT03348540
Lead Sponsor
Creighton University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
89
Inclusion Criteria
  • significant symptoms of PTSD and qualifying traumatic event
Exclusion Criteria
  • new traumatic event within one month of beginning the trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Comparison TaskComparison Task6 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).
Attention Control TrainingAttention Control Training* 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).
Primary Outcome Measures
NameTimeMethod
Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test10 minute long administration, given twice to measure change scores from pre and post training approximately 1 month apart

PTSD self-report questionnaire

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Creighton Univeristy

🇺🇸

Omaha, Nebraska, United States

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