Information Processing Modification in PTSD (Oct. 18)
1 other identifier
interventional
37
1 country
1
Brief Summary
The purpose of this study is to determine whether a computerized intervention designed to change the nature of attention biases will be effective in reducing the symptoms of post traumatic stress disorder (PTSD) in American combat veterans returning from the wars in Afghanistan and Iraq.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2012
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
January 15, 2008
CompletedFirst Posted
Study publicly available on registry
January 28, 2008
CompletedStudy Start
First participant enrolled
July 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2012
CompletedResults Posted
Study results publicly available
February 4, 2014
CompletedFebruary 4, 2014
July 1, 2009
Same day
January 15, 2008
December 13, 2013
December 13, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Post-Traumatic Stress Disorder Checklist-Military Version (PCL-M)
The PCL-M is a 17-item questionnaire that assesses the severity of PTSD symptoms using a 5-point Likert scale ranging from "not at all" to "extremely," with a minimum score of 17 and a maximum score of 85 (Weathers, Litz, Herman, Huska, \& Keane, 1993). Participants are asked to rate to what extent they experienced PTSD symptoms over the previous month due to prior combat experiences. The military version of the PCL (PCL-M) refers specifically to a traumatic military related event (Weathers, Litz, Huska, \& Keane, 1994). Research suggests that the PCL-M has good test-retest reliability (r = .70) and internal consistency (alpha = .97; Weathers et al., 1993).
Pre, Post, Followup
Study Arms (2)
1 Attention Bias Modification (ABM)
EXPERIMENTALThe ABM comprised a probe detection paradigm described above, modified to facilitate the allocation of attention away from threatening material. In this task, the probe always replaced the neutral word. Stimuli comprised a different set of 12 threat-neutral word pairs different than those used in the attention bias assessment. Participants completed 288 training trials: 2 (probe type) x 2 (probe location) x 2 (threat location) x 12 (threat-neutral word pairs) x 3 (repetition). Thus, although there were no explicit instructions to direct attention away from threat words, on all trials, the position of the neutral word indicated the position of the probe.
2 Attention Control Condition (ACC)
PLACEBO COMPARATORThe ACC condition was identical to the ABM procedure with the exception that the probe appeared with equal frequency in the position of the threat and neutral words, such that attention was neither trained towards nor away from threat.
Interventions
The ABM comprised a probe detection paradigm described above, modified to facilitate the allocation of attention away from threatening material. In this task, the probe always replaced the neutral word. Stimuli comprised a different set of 12 threat-neutral word pairs different than those used in the attention bias assessment. Participants completed 288 training trials: 2 (probe type) x 2 (probe location) x 2 (threat location) x 12 (threat-neutral word pairs) x 3 (repetition). Thus, although there were no explicit instructions to direct attention away from threat words, on all trials, the position of the neutral word indicated the position of the probe.
The ACC condition was identical to the ABM procedure with the exception that the probe appeared with equal frequency in the position of the threat and neutral words, such that attention was neither trained towards nor away from threat.
Eligibility Criteria
You may qualify if:
- Primary DSM-IV-TR Axis I diagnosis of post-traumatic stress disorder
- Combat veteran from Iraq and/or Afghanistan
You may not qualify if:
- No change in medication type or dose during the twelve weeks prior to treatment
- No current psychotherapy
- No evidence of suicidal intent
- No evidence of current substance dependence in the past 6 months
- No evidence of current or past schizophrenia, bipolar disorder, or organic mental disorder
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Center for Understanding and Treating Anxiety
San Diego, California, 92120, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Nader Amir
- Organization
- San Diego State University/University of California Joint Doctoral Program in Clinical Psychology
Study Officials
- PRINCIPAL INVESTIGATOR
Nader Amir, PhD
San Diego State University
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
January 15, 2008
First Posted
January 28, 2008
Study Start
July 1, 2012
Primary Completion
July 1, 2012
Study Completion
July 1, 2012
Last Updated
February 4, 2014
Results First Posted
February 4, 2014
Record last verified: 2009-07