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Cognitive Training for Post Traumatic Stress Disorder: Effects on Cognitive, Emotional, and Brain Function

Cognitive Training for PTSD: Effects on Cognitive, Emotional, and Brain Function

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01644851
Enrollment
40
Registered
2012-07-19
Start date
2012-07-31
Completion date
2015-07-31
Last updated
2014-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posttraumatic Stress Disorders

Keywords

veterans, neuropsychology, neuroimaging, attention, working memory, inhibition, magnetic resonance imaging, functional, trauma, stress, anxiety, emotion, prefrontal cortex

Brief summary

The purpose of this pilot study is to determine the effects of computer-based training in executive functioning compared to word games on cognitive and emotional aspects of combat-related PTSD.

Detailed description

Many posttraumatic stress disorder (PTSD) patients either choose not to complete or do not achieve optimal response to current first-line behavioral and pharmacologic treatments. Neurocognitive research points to the potential of novel treatments targeting dorsal prefrontal function and inhibition, attention, and working memory processes. This study investigates effects of computer-based training in executive functions compared to word games on cognitive and emotional aspects of combat-related PTSD. Paper-and-pencil questionnaires, interviews, computer-administered testing, and magnetic resonance imaging will be complete before and after the intervention. Results from this pilot study will provide information concerning feasibility and treatment potential of cognitive training for PTSD.

Interventions

Computer-based training in executive functions, administered via www.lumosity.com website.

Sponsors

University of Kansas
CollaboratorOTHER
University of Missouri, Kansas City
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* combat veterans who served in Operation Iraqi Freedom, Operation Enduring Freedom, or Operation New Dawn

Exclusion criteria

* enrolled in other active treatment protocols * current substance abuse or dependence * current suicidal ideation * diagnosis of a neurological disorder * history of moderate to severe traumatic brain injury

Design outcomes

Primary

MeasureTime frame
Neural activity in prefrontal regions during cognitive and emotional processing measured by functional magnetic resonance imaging.change from baseline to after 6 weeks of training

Secondary

MeasureTime frame
Cognitive functioning as measured by neuropsychological assessment.change from baseline to after 6 weeks of training

Other

MeasureTime frame
Clinical PTSD symptoms as measured by the Clinician Administered PTSD Scale (CAPS).change from baseline to after 6 weeks of training

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026