- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03696225
Assessment and Treatment of Cognitive Functioning Deficits in Veterans With PTSD (CCTPTSD)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Project Background: PTSD is associated with deficits in cognitive functioning including memory, learning, processing speed, concentration, attention, and executive functioning. Though many Veterans benefit from evidence-based psychotherapy (EBP) for PTSD, many Veterans have cognitive functioning deficits even after completing EBP for PTSD. There are no evidence-based treatments for these Veterans. Compensatory Cognitive Training (CCT) is improves cognitive functioning in Veterans with brain injury history, but is not yet tested in Veterans with PTSD.
Project Aims: This study will evaluate feasibility, acceptability, and participant characteristics, and estimate effect sizes, in a pilot test of CCT for Veterans with PTSD-related cognitive problems. Data from this study will form the basis for a future, fully powered trial testing the effectiveness of CCT for cognitive problems in Veterans with PTSD.
Project Methods: The investigators will recruit Veterans from local VA mental health clinics, using the VA's Corporate Data Warehouse (CDW) to identify potentially eligible Veterans if needed. The investigators will compare CCT vs. treatment as usual for 36 Veterans with PTSD-related cognitive functioning deficits. The investigators will calculate rates of recruitment, retention, and intervention participation. Statistical significance will be examined, though the investigators' focus will be on effect size estimates, score ranges, and variability to plan for a follow-up, fully powered RCT.
Anticipated Impact: PTSD-related cognitive functioning deficits are a significant problem for many Veterans. CCT is an effective cognitive rehabilitation intervention for Veterans with a history of brain injury, but VA clinicians need data on its effectiveness for Veterans with PTSD-related cognitive functioning deficits. These studies will provide the data necessary for a larger scale RCT proposal if results show that CCT is as promising as expected for Veterans with PTSD.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Oregon
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Portland, Oregon, United States, 97207-2964
- VA Portland Health Care System, Portland, OR
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Eligible Veterans must meet Diagnostic and Statistical Manual 5 (DSM-5) criteria for PTSD with evidence-based PTSD treatment participation within the past 2 years.
- Must have an individual mental health provider/case manager assigned for coordination of care and management of crises as well as provision of treatment as usual if Veteran is randomly assigned to this condition.
- Report subjective cognitive complaints, such as problems with memory, attention/concentration, and executive function (e.g., planning, organization, problem-solving, decision-making).
- Referring provider observes mild cognitive problems that interfere with daily life (e.g., forgetting appointments or medications, poor performance at work or school, difficulty remembering information, trouble focusing in treatment sessions, trouble following through on goals).
- Fluent English speaker.
- Able to read and write and provide informed consent.
Exclusion Criteria:
- No history of traumatic brain injury (tbi) of any severity or another major medical condition likely to significantly impact cognitive functioning such as stroke, multiple sclerosis (MS), Parkinson's, or a brain tumor.
- Do not meet criteria for bipolar disorder or a psychotic disorder. Do not have a diagnosis of a substance dependence disorder within the past 30 days.
- Do not have active suicidal intent indicating significant clinical risk (which would suggest that a treatment targeting suicidal intent is indicated).
- Cognitive problems are not severe (i.e., no dementia). Cognitive problems do NOT interfere with a Veteran's overall ability to live independently or care for him/herself.
- Not currently participating in any type of brain stimulation treatment.
- No significant auditory/visual impairments.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Compensatory Cognitive Training (CCT)
Compensatory Cognitive Training draws from the theoretical literature on compensatory strategy training for other cognitively impaired populations (e.g., Huckans et al., 2013; Twamley et al., 2010; Storzbach et al., 2016).
It is a rehabilitation model that aims to teach individuals strategies that allow them to work around cognitive deficits.
Consistent with this model and the expert recommendations for civilians and Service members with TBI (Cicerone, 2011), manualized CCT treatment provides training in compensatory attention and learning/memory skills, formal problem-solving strategies applied to daily problems, and the use of external aids such as calendar systems and assistive devices to promote completion of daily tasks (Storzbach et al., 2016).
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Compensatory Cognitive Training draws from the theoretical literature on compensatory strategy training for other cognitively impaired populations (e.g., Huckans et al., 2013; Twamley et al., 2010; Storzbach et al., 2016).
It is a rehabilitation model that aims to teach individuals strategies that allow them to work around cognitive deficits.
Consistent with this model and the expert recommendations for civilians and Service members with TBI (Cicerone, 2011), manualized CCT treatment provides training in compensatory attention and learning/memory skills, formal problem-solving strategies applied to daily problems, and the use of external aids such as calendar systems and assistive devices to promote completion of daily tasks (Storzbach et al., 2016).
Other Names:
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Active Comparator: Treatment as Usual (TAU)
All TAU participants have an ongoing VA mental health provider and received ongoing mental health care during the course of the study (generally weekly individual or group sessions focusing on evidence-based PTSD treatment).
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All TAU participants have an ongoing VA mental health provider and received ongoing mental health care during the course of the study (generally weekly individual or group sessions focusing on evidence-based PTSD treatment).
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Prospective-Retrospective Memory Questionnaire (PRMQ; Crawford et al., 2006)
Time Frame: change from baseline to 3 and 6 months
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Self-report severity measure of prospective (remembering to do something in the future) and retrospective (remembering something from the past) memory problems relevant to every day life.
Higher scores represent worse outcomes.
Total score ranges from 0-64.
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change from baseline to 3 and 6 months
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Multiple Sclerosis Neuropsychological Screening Questionnaire - Patient Version (MSNQ; Benedict et al., 2003)
Time Frame: change from baseline to 3 and 6 months
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Self-report severity measure of attention and organizational problems.
Scores on the MSNQ range from 0 to 58, with higher scores indicating greater cognitive impairment.
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change from baseline to 3 and 6 months
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California Verbal Learning Test (CVLT-II; Delis et al., 2000)
Time Frame: change from baseline to 3 and 6 months
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Comprehensive measurement of verbal learning and memory and includes a forced choice validity.
The total raw score is the sum of correct responses on the five presentations; scores range from 0-80.
Higher scores represent better outcomes.
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change from baseline to 3 and 6 months
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Wechsler Adult Intelligence Scale (WAIS-IV) Coding Subtest (Wechsler, 2008)
Time Frame: change from baseline to 3 and 6 months
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A measure of processing speed.
Higher scores represent better outcomes.
Scores range from 0-155.
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change from baseline to 3 and 6 months
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Controlled Oral Word Association Test (Benton, Hamsher, & Sivan, 1983)
Time Frame: change from baseline to 3 and 6 months
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The Controlled Oral Word Association (COWA) Test measures word generation, verbal fluency, and executive functioning.
Participants are asked to name as many words as they can starting with a specific letter (i.e., F, A, S) within one minute, and as many words as possible in a specified category (i.e., animals) within one minute.
Total score is the sum of responses (three letter trials, one category trial).
Higher scores represent better outcomes.
Total score ranges are affected by age and education.
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change from baseline to 3 and 6 months
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Halstead Reitan Trailmaking Test (Trails A & B; Reitan & Wolfson, 1985)
Time Frame: change from baseline to 3 and 6 months
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Measures visual tracking, processing speed, and executive functioning.
Scores represent the amount of time to complete the task (in seconds), range from 10-366, and higher numbers represent worse outcomes.
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change from baseline to 3 and 6 months
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World Health Organization Disability Assessment Scale (WHODAS 2.0)
Time Frame: change from baseline to 3 and 6 months
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Self-report measure of quality of life and global functioning.
Higher scores represent worse outcomes.
Total score ranges from 0-144.
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change from baseline to 3 and 6 months
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Quality of Life in Neurological Disorders (Neuro-QOL): Cognitive, Ability to Participate in Social Roles and Activities, and Sleep Scales
Time Frame: change from baseline to 3 and 6 months
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Self-report measure of quality of life, cognitive functioning, sleep functioning, and social functioning.
Higher scores represent lower functioning.
Total scores range from 52 to 260.
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change from baseline to 3 and 6 months
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Memory Compensation Questionnaire (MCQ; de Frias & Dixon, 2005)
Time Frame: change from baseline to 3 and 6 months
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A 44-item self-report questionnaire that rates the extent of use of various strategies to improve memory performance relevant to daily living.
Higher scores represent better outcomes.
Total score ranges from 0-176.
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change from baseline to 3 and 6 months
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Portland Cognitive Strategies Scale 2.0 (PCSS)
Time Frame: change from baseline to 3 and 6 months
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Measures compensatory cognitive strategy use through two scales; how often skills are used and how useful.
Higher scores represent more skill use and more perceived usefulness.
Total score ranges from 0-60 per scale.
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change from baseline to 3 and 6 months
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Wechsler Adult Intelligence Scale (WAIS-IV) Digit Span Subtest (Wechsler, 2008)
Time Frame: change from baseline to 3 and 6 months
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Measures attention, working memory, processing speed, and reliable digit span validity.
Higher scores represent better outcomes.
Scores on each subtest (forward, backward, and sequential) range from 0-16 and are reported as WAIS Scaled Scores.
Total score (range 0-48) is the sum of each subtest.
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change from baseline to 3 and 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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PTSD Checklist (PCL-5; Weathers et al., 2013)
Time Frame: change from baseline to 3 and 6 months
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PTSD symptoms and severity.
Higher scores indicates more severe symptomology.
Total score ranges from 0-80.
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change from baseline to 3 and 6 months
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Patient Health Questionnaire (PHQ-9; Spitzer, Kroenke, & Williams, 1999)
Time Frame: change from baseline to 3 and 6 months
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A brief, nine-item depression assessment questionnaire used to screen for depression and monitor its severity.
Higher scores represent worse outcomes.
Total score ranges from 0-27.
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change from baseline to 3 and 6 months
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Collaborators and Investigators
Investigators
- Principal Investigator: Maya Elin O'Neil, PhD MS, VA Portland Health Care System, Portland, OR
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- D2762-W
- 1IK2RX002762-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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