DoD PTSD November 13 - Information Processing Modification in the Treatment of PTSD
Information Processing Modification in the Treatment of PTSD
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
San Diego, California, United States, 92120
- Center for Understanding and Treating Anxiety
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Primary DSM-IV-TR Axis I diagnosis of post-traumatic stress disorder
- Combat veteran from Iraq and/or Afghanistan
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: 1 Attention Bias Modification (ABM)
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 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.
|
|
Placebo Comparator: 2 Attention Control Condition (ACC)
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.
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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.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Post-Traumatic Stress Disorder Checklist-Military Version (PCL-M)
Time Frame: Pre-Treatment, Post-Treatment (after 4 weeks of treatment)
|
The PCL-5 is a 20-item self-report measure that assesses the 20 DSM-5 symptoms of PTSD.
Scores range from 0 to 80, with higher scores indicating more severe symptoms.
|
Pre-Treatment, Post-Treatment (after 4 weeks of treatment)
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Nader Amir, PhD, San Diego State University
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- PT075321 (Other Identifier: Department of Defense)
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