- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03490110
Brain Markers of Improvements in Cognitive Functioning
EEG Markers of Training-Induced Improvements in Cognitive Functioning
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Detailed Description: Traumatic brain injuries (TBI) can impair cognitive functioning long after the initial trauma. Some of the most common, persistent, and disabling consequences of traumatic brain injury are deficits in higher order cognitive functions that direct more basic processes based on an individual's goals. Symptoms such as distractibility and difficulty holding goal-relevant information in memory can affect achievement of personal and professional goals. These cognitive problems can be exacerbated by post-traumatic stress (PTS) symptoms, commonly observed in the Veteran population. Interventions that strengthen goal-directed regulation of cognitive-emotion states could have far reaching benefits for Veterans.
One challenge in rehabilitation is that response to training can be highly variable, and a better understanding of the neural bases for this variability could inform patient care. Investigators have developed a system for training neurocognitive skills that can be used in rehabilitation neuroscience studies to elucidate the neural bases of improvements in cognitive functioning. The training system is designed to help patients improve goal-directed brain state regulation, and preliminary work has investigated brain network parameters that may predict response to training. Electroencephalography (EEG) potentially provides easily accessible markers for the neural bases of improvements with training.
Objectives in this pilot study are to investigate the potential of EEG markers to: (1) explain differential responses to attention regulation training; and (2) predict responses to training.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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Sacramento, California, United States, 95655
- VA Northern California Health Care System, Mather, CA
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Veterans
- History of TBI (as defined by the American Congress of Rehabilitation Medicine and VA, with reported plausible mechanism of head injury, loss of consciousness with some period of posttraumatic alteration in cognition), in the chronic, stable phase of recovery (>6 months from injury)
- On stable psychoactive medications (> 30 days)
- Able and willing to participate in EEG, training and, assessments
Exclusion Criteria:
- Severely apathetic/abulic, aphasic, or other reasons for being unable or unwilling to participate with the training tasks
- Severe cognitive dysfunction
- History of neurodevelopmental abnormalities
- Ongoing illicit drug or alcohol abuse
- Schizophrenia
- Bipolar disorder
- History of other neurological disorders
- Current medical illnesses that may alter mental status or disrupt participation in the study
- Active psychotropic medication changes
- There will be no restriction in regard to gender, race, and socioeconomic status
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: State regulation skill training
This arm utilizes a training system designed to strengthen goal-directed cognitive-emotional state regulation skills.
The emphasis is on practice and active application of skills across a range of challenge contexts.
Digital scenarios provide experiential learning opportunities, allowing Veterans to apply skills to tackle challenges that are calibrated to maximize learning.
Coaches guide learning for successful application of skills to challenges in personal life.
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Participants complete seven supervised training sessions.
Training sessions last 2 hours, and participants are requested to complete approximately 2.5 hours of additional skill practice over the course of each week outside of session (total ~4.5 hours per week).
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Active Comparator: Treatment-as-usual
In this arm, participants receive clinical care as usual in VA and other clinics.
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Participants receive clinical care as usual over a matched time period.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Composite Score of Attention and Executive Functioning From a Neurocognitive Test Battery
Time Frame: Week 1, before intervention period (baseline)
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The investigators created a composite score based upon standardized performance on the following neurocognitive measures of attention and executive functions: Wechsler Adult Intelligence Test - 4th Edition- letter number sequence; Auditory Consonant Trigrams - 9, 18, 36 second conditions; Digit Vigilance Test - Total Errors; Delis-Kaplan Executive Function System Color-Word Interference Trials 3 and 4 - Time and Total Errors; & Trails B - Time. Performance on each measure was scored using populations norms, and these scores are then standardized (Z-scored) and averaged to create a composite outcome (the unit measure being Z-score). A Z-score reflects the number of standard deviations a given score is away from the population mean: A Z-score of 0 is equal to the population mean, with positive and negative values reflecting performances above and below the population mean, respectively. |
Week 1, before intervention period (baseline)
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Composite Score of Attention and Executive Functioning From a Neurocognitive Test Battery
Time Frame: Week 8, after the intervention period
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The investigators created a composite score based upon standardized performance on the following neurocognitive measures of attention and executive functions: Wechsler Adult Intelligence Test - 4th Edition- letter number sequence; Auditory Consonant Trigrams - 9, 18, 36 second conditions; Digit Vigilance Test - Total Errors; Delis-Kaplan Executive Function System Color-Word Interference Trials 3 and 4 - Time and Total Errors; & Trails B - Time. Performance on each measure was scored using populations norms, and these scores are then standardized (Z-scored) and averaged to create a composite outcome (the unit measure being Z-score). A Z-score reflects the number of standard deviations a given score is away from the population mean: A Z-score of 0 is equal to the population mean, with positive and negative values reflecting performances above and below the population mean, respectively. Change will be analyzed for this data as change from before to after the intervention period. |
Week 8, after the intervention period
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Event-Related Potential (ERP) Related to Memory Retrieval (Measured in uV)
Time Frame: Week 8, after the intervention period
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Electroencephalography (EEG) will be collected during tasks that require attention and working memory.
The old/new ERP effect (difference between brain responses to correctly remembered studied items vs. correctly rejected unstudied items) will be analyzed for this data as change from before to after the intervention period.
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Week 8, after the intervention period
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Event-Related Potential (ERP) Related to Memory Retrieval (Measured in uV)
Time Frame: Week 1, before the intervention period
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Electroencephalography (EEG) will be collected during tasks that require attention and working memory.
The old/new ERP effect (difference between brain responses to correctly remembered studied items vs. correctly rejected unstudied items) will be analyzed for this data prior to the intervention period.
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Week 1, before the intervention period
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Network Modularity From EEG
Time Frame: Week 8, after the intervention period
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EEG will be collected during a focused rest condition.
Network modularity will be estimated from a matrix of connections between electrodes based on phase coherence, a unit-less measure of correlation between phase angles of EEG signals in the theta (4-8 Hz) frequency range.
The modularity metric reflects the strength of modular network organization by summing the difference between the fraction of within-module connections to the total fraction of connections across modules, thus ranging from 0 (random) to 1 (completely modular).
Change in network modularity will be analyzed for this data as change from before to after the intervention period.
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Week 8, after the intervention period
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Anthony Chen, MD MA, VA Northern California Health Care System, Mather, CA
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- N2240-P
- 16-12-00774 (Other Grant/Funding Number: VA Northern California Health Care System)
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.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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