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Developing Process-Specific Verbal Memory Interventions for Veterans With Tramatic Brain Injury (TBI) (DPSVM)

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Memory Strategy Training
Errorless Learning
Retrieval Practice
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury focused on measuring TBI, memory disorder, injury, brain, traumatic, rehabilitation

Eligibility Criteria

25 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Veterans aged 25-65 who are post-deployment,
  • having served in Operation Iraqi Freedom (OIF), Operation Enduring Freedom (OEF), or Operation New Dawn (OND),
  • who meet criteria for moderate or severe TBI during deployment,
  • are eligible to participate.
  • Patients will meet the 2007 VA/DoD criteria54,

    • supplemented by data from the VA TBI Identification Semi-Structured Interview55.
  • All patients will have gone through Level I and II assessments with positive findings.
  • Primary inclusion criteria:

    • Moderate to Severe Traumatic Brain Injury (M-STBI) (blast and blunt),
    • > 6 months post-injury,
    • no receptive aphasia (impairing ability to comprehend task instructions),
    • able to participate in return visits.

Exclusion Criteria:

  • Primary exclusion criteria:

    • No MRI contraindications,
    • not claustrophobic,
    • no current or past history of disabling Axis I psychiatric disorders (except for PTSD and depression),
    • no active substance abuse,
    • not pregnant.

Sites / Locations

  • North Florida/South Georgia Veterans Health System, Gainesville, FL

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Memory Strategy Training

Errorless Learning

Retrieval Practice

Arm Description

This arm involves intervention that teaches participants to use active encoding strategies to learn and remember new information.

This arm involves intervention that enhances consolidation of correct target information by preventing false recall of incorrect information during the acquisition phase.

This arm involves intervention that enhances retrieval of correct target information by actively practicing retrieval in the presence of a cue.

Outcomes

Primary Outcome Measures

Change in performance on paired-associate learning of words and face-name pairs
Participants will be tested each session on paired-associate learning (words and face-name pairs) for trained and untrained items
Change in functional brain connectivity within memory-relevant brain networks
Participants will undergo MRI scanning before and after memory interventions to assess the effect of intervention on functional brain connectivity in default mode network (DMN), task-positive network (TPN), and salience network (SN)

Secondary Outcome Measures

Mayo-Portland Adaptability Inventory (MPAI-4)
This measure assesses the overall impact of TBI on functional capacity
RAVLT
This is an independent measure of list learning designed to assess the effect of memory intervention on learning of untrained items.
Brief Visuo-Spatial Learning Test-Revised (BVLT-R)
This is a measure of nonverbal memory (drawing from memory), designed to assess the effect of memory intervention on learning and memory for untrained items.
Ecologically Oriented Neurorehabilitation of Memory (EON-MEM) Everyday Memory Simulations
These are tasks of everyday memory designed to assess whether effects of memory intervention generalize to real-world memory tasks.
Quality of Life after Brain Injury (QOLIBRI)
This is a quality of life measure after brain injury, designed to assess whether effects of memory intervention extend to quality of life.
PROMIS and Neuro-QOL Item Banks
These items assess outcome from the patient perspective (patient-reported outcomes)
Satisfaction with Life Scale (SWLS)
This questionnaire assesses overall life quality and satisfaction.

Full Information

First Posted
November 19, 2014
Last Updated
April 4, 2022
Sponsor
VA Office of Research and Development
Collaborators
University of Florida
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1. Study Identification

Unique Protocol Identification Number
NCT02310633
Brief Title
Developing Process-Specific Verbal Memory Interventions for Veterans With Tramatic Brain Injury (TBI)
Acronym
DPSVM
Official Title
Developing Process-Specific Verbal Memory Interventions for Veterans With TBI
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
January 5, 2015 (Actual)
Primary Completion Date
December 22, 2017 (Actual)
Study Completion Date
December 29, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
University of Florida

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Blast-related and blunt traumatic brain injury is a key priority area of Rehabilitation Research & Development (RR&D) and represents a critically important public health problem facing the Veteran population. Developing efficacious treatments for persistent memory deficits seen in this population is a key step in reducing the impact that such problems have in the everyday lives of Veterans. Memory problems after TBI in Veterans are quite heterogeneous, and efficacy will likely be maximized by developing and disseminating multiple alternative treatments individually matched to the Veteran's key deficits, and by research that seeks to understand the cognitive and neural basis of treatment-related change over time. The results of this approach may aid clinical decision making and assignment of patients to rehabilitative treatments most likely to improve memory capacity and functional outcome.
Detailed Description
Memory dysfunction can result from impairments along a continuum of information processing, from poor initial acquisition of information during learning to disturbed retrieval of stored memory when it is later needed to perform a task1. The heterogeneous nature of TBI-related memory impairment is well-known, and there is a critical need to better understand such disease heterogeneity in order to enhance diagnosis and therapeutic management2. Several subtypes of memory dysfunction after TBI have been identified3,4. First, some TBI survivors exhibit impaired memory acquisition/encoding (e.g., frontal system damage)5. Second, some exhibit impaired memory consolidation/storage impairment (e.g., prominent damage to temporal lobe systems6). Third, some show impairment in retrieval of information5,7. This heterogeneity results from the variable nature and severity of underlying brain trauma resulting from unpredictable mechanical forces2,8. It has been suggested that parsing this underlying variability should take precedence over generalities regarding the effect of TBI on memory when conceptualizing or treating memory disorders in this population8 Nevertheless, many rehabilitation programs utilize a "one size fits all" approach to memory training, based (typically) on training compensatory strategies, with no training specifically targeted to the identifiable component processes of memory that could be differentially impaired (encoding, consolidation/storage, and retrieval), and which might respond differentially to more specifically targeted treatment. This situation in clinical practice is due to the lack of evidence upon which to base informed decision-making in allocating specifically targeted memory re-training for individual survivors of TBI, based on clinical test results identifying which memory component processes are impaired (encoding, consolidation/storage, and retrieval). Because of this, there is little attempt to appropriately match patient impairment to targeted treatments. There are existing training protocols for training these three components of memory processing, as follows: encoding (memory strategy training9), consolidation (errorless learning10), and retrieval (retrieval practice11, but their efficacy has not been tested in TBI survivors with documented impairments in each component. That is, to the investigators' knowledge, there is no solid evidence for memory training in TBI survivors that supports the widely held belief that specifically matching the patient impairment to the treatment leads to better treatment outcomes. This proposal attempts to fill this gap in the investigators' knowledge. Prior to testing the efficacy of these three types of training in a large trial, it is important to make standard preparations, such as refining and testing training materials and ensuring fidelity of treatment methods across clinicians. Aim 1. Aim 1 is to refine and validate three separate, process-specific memory rehabilitation treatments that focus on improving information-processing at the encoding, consolidation, or retrieval stage for Veterans with chronic moderate/severe TBI. Objective 1.1. Generate treatment manuals for three process-specific memory treatments. Objective 1.2. Test and refine treatment fidelity so that each of the three interventions can be reliably delivered by different clinicians. Aim 2. Aim 2 is to provide a preliminary test of the response to the three memory interventions. At baseline, TBI survivors will be evaluated for memory function in each of these three memory component processes using established neuropsychometric methods. Their experimental treatment allocation will be to the treatment targeting their most impaired memory component. In addition, each subject will serve as his/her own control, by engaging in a treatment targeted to another memory component ('mismatched' group). Hypothesis A. Matched vs. mismatched group will show differential improvement in memory component function, with the former group benefitting to a significantly greater degree. (Primary measures: Memory component performance, encoding, consolidation, retrieval; secondary: cognitive function and quality of life). Aim 3. Aim 3 is to establish links between the behavioral taxonomy of the three memory components and differences in brain structure and function documented with diffusion tensor imaging and functional connectivity analysis. This is a key first step in establishing brain-based metrics of neuroplastic change after memory therapy in the investigators' research program. Objective 3.1. Identify specific and unique imaging signatures that distinguish patients with deficits in encoding, consolidation, and retrieval, respectively. Primary measures: structural measures of morphometry and white matter integrity (FA) and functional connectivity (cross correlation and total interdependence) in identified brain networks damaged in TBI. Clinical Implications. This research has the potential to devise a method to match specific subcomponents of memory impairment to specifically targeted memory interventions, thus maximizing recovery of memory and function. The results of this investigation will be used to refine the interventions, to evaluate cognitive and functional endpoints, and to power a larger clinical trial that will yield data enabling clinicians to match TBI patients to effective treatments based on their individual profile of memory dysfunction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury
Keywords
TBI, memory disorder, injury, brain, traumatic, rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Memory Strategy Training
Arm Type
Active Comparator
Arm Description
This arm involves intervention that teaches participants to use active encoding strategies to learn and remember new information.
Arm Title
Errorless Learning
Arm Type
Active Comparator
Arm Description
This arm involves intervention that enhances consolidation of correct target information by preventing false recall of incorrect information during the acquisition phase.
Arm Title
Retrieval Practice
Arm Type
Active Comparator
Arm Description
This arm involves intervention that enhances retrieval of correct target information by actively practicing retrieval in the presence of a cue.
Intervention Type
Behavioral
Intervention Name(s)
Memory Strategy Training
Intervention Description
This intervention involves intervention that teaches participants to use active encoding strategies to learn and remember new information. The intervention will be implemented using verbal and face-name paired associate learning.
Intervention Type
Behavioral
Intervention Name(s)
Errorless Learning
Intervention Description
This intervention enhances consolidation of correct target information by preventing false recall of incorrect information during the acquisition phase. Participants are encouraged to recall target information only if they are sure it is correct, thus eliminating errors. The intervention will be implemented using verbal and face-name paired associate learning.
Intervention Type
Behavioral
Intervention Name(s)
Retrieval Practice
Intervention Description
This intervention enhances retrieval of correct target information by actively practicing retrieval in the presence of a cue. The intervention will be implemented using verbal and face-name paired associate learning.
Primary Outcome Measure Information:
Title
Change in performance on paired-associate learning of words and face-name pairs
Description
Participants will be tested each session on paired-associate learning (words and face-name pairs) for trained and untrained items
Time Frame
At the end of each session (twice weekly), up to 12 weeks
Title
Change in functional brain connectivity within memory-relevant brain networks
Description
Participants will undergo MRI scanning before and after memory interventions to assess the effect of intervention on functional brain connectivity in default mode network (DMN), task-positive network (TPN), and salience network (SN)
Time Frame
Prior to start of intervention (Week 0) and again at the end of intervention (Week 8)
Secondary Outcome Measure Information:
Title
Mayo-Portland Adaptability Inventory (MPAI-4)
Description
This measure assesses the overall impact of TBI on functional capacity
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)
Title
RAVLT
Description
This is an independent measure of list learning designed to assess the effect of memory intervention on learning of untrained items.
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)
Title
Brief Visuo-Spatial Learning Test-Revised (BVLT-R)
Description
This is a measure of nonverbal memory (drawing from memory), designed to assess the effect of memory intervention on learning and memory for untrained items.
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)
Title
Ecologically Oriented Neurorehabilitation of Memory (EON-MEM) Everyday Memory Simulations
Description
These are tasks of everyday memory designed to assess whether effects of memory intervention generalize to real-world memory tasks.
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)
Title
Quality of Life after Brain Injury (QOLIBRI)
Description
This is a quality of life measure after brain injury, designed to assess whether effects of memory intervention extend to quality of life.
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)
Title
PROMIS and Neuro-QOL Item Banks
Description
These items assess outcome from the patient perspective (patient-reported outcomes)
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)
Title
Satisfaction with Life Scale (SWLS)
Description
This questionnaire assesses overall life quality and satisfaction.
Time Frame
Week 0, Week 8, and 1 month after treatment is concluded (Week 12)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Veterans aged 25-65 who are post-deployment, having served in Operation Iraqi Freedom (OIF), Operation Enduring Freedom (OEF), or Operation New Dawn (OND), who meet criteria for moderate or severe TBI during deployment, are eligible to participate. Patients will meet the 2007 VA/DoD criteria54, supplemented by data from the VA TBI Identification Semi-Structured Interview55. All patients will have gone through Level I and II assessments with positive findings. Primary inclusion criteria: Moderate to Severe Traumatic Brain Injury (M-STBI) (blast and blunt), > 6 months post-injury, no receptive aphasia (impairing ability to comprehend task instructions), able to participate in return visits. Exclusion Criteria: Primary exclusion criteria: No MRI contraindications, not claustrophobic, no current or past history of disabling Axis I psychiatric disorders (except for PTSD and depression), no active substance abuse, not pregnant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Russell M Bauer, PhD
Organizational Affiliation
North Florida/South Georgia Veterans Health System, Gainesville, FL
Official's Role
Principal Investigator
Facility Information:
Facility Name
North Florida/South Georgia Veterans Health System, Gainesville, FL
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32608
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be available to other researchers in a de-identified, password protected file.
Links:
URL
http://www.brrc.research.va.gov
Description
Home page for the Gainesville VA Brain Rehabilitation Research Center of Excellence

Learn more about this trial

Developing Process-Specific Verbal Memory Interventions for Veterans With Tramatic Brain Injury (TBI)

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