Posttraumatic Stress Disorder Clinical Trial
Official title:
Cognitive Remediation in PTSD
Verified date | February 2012 |
Source | Bronx VA Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Federal Government |
Study type | Interventional |
The purpose of this study is to gather feasibility data on cognitive remediation therapy (CRT) as an alternative intervention for PTSD. CRT is a standardized intervention that involves performing cognitive exercises to improve attention, processing speed, and memory through practice. Although the primary objective will be to determine the effect of CRT on cognitive functioning in PTSD, data on PTSD symptom severity and other clinical measures will also be examined to assess whether and to what degree cognitive alterations and symptom severity might be linked. CogPack, a computer-based form of CRT, would be employed for this project. Participants will be randomized to receive CRT or to play the video game Tetris as a control condition.
Status | Completed |
Enrollment | 2 |
Est. completion date | March 2011 |
Est. primary completion date | March 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Male and female combat veterans with a current diagnosis of PTSD with a minimum duration of six months - Age 18 years and older - Capable of understanding, reading, and writing in English Exclusion Criteria: - Incapable and/or unwilling to provide written informed consent prior to participation - Less than 11 years of formal education - The veteran, the veteran's physician, or the study physician thinks that the veteran's clinical state necessitates hospitalization - Response of 3 or 4 on the suicidality items of the Hamilton Depression Rating Scale or an assessed serious suicide risk - Current substance and/or alcohol abuse and/or dependence, or abuse/dependence within the previous 6 months which contraindicates participation in the judgment of the evaluating clinician - A lifetime history of schizophrenia, schizoaffective disorder, bipolar disorder, organic mental disorder, or dementia |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | James J. Peters Veterans Affairs Medical Center | Bronx | New York |
Lead Sponsor | Collaborator |
---|---|
Bronx VA Medical Center | VISN 3 Mental Illness Research, Education and Clinical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cognitive functioning, assessed by Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery and portions of Wechsler Adult Intelligence Scale III (WAIS-III) and Wechsler Memory Scale III (WMS-III) | 10 weeks | No | |
Secondary | PTSD symptom severity, assessed by Clinician Administered PTSD Scale (CAPS) | 10 weeks | No |
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