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Clinical Trials/NCT03348540
NCT03348540
Completed
Not Applicable

Randomized Clinical Trial of Attention Control Training for Symptoms of PTSD in Children

Creighton University1 site in 1 country89 target enrollmentNovember 20, 2017
ConditionsPTSD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
PTSD
Sponsor
Creighton University
Enrollment
89
Locations
1
Primary Endpoint
Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test
Status
Completed
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
November 20, 2017
End Date
November 20, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amy Badura Brack

Professor of Psychology

Creighton University

Eligibility Criteria

Inclusion Criteria

  • significant symptoms of PTSD and qualifying traumatic event

Exclusion Criteria

  • new traumatic event within one month of beginning the trial

Outcomes

Primary Outcomes

Change in posttraumatic stress disorder (PTSD) symptoms from pre to post test

Time Frame: 10 minute long administration, given twice to measure change scores from pre and post training approximately 1 month apart

PTSD self-report questionnaire

Study Sites (1)

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