Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT02310633 |
| Other study ID # |
N1730-P |
| Secondary ID |
1I21RX001730-01 |
| Status |
Completed |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
January 5, 2015 |
| Est. completion date |
December 29, 2017 |
Study information
| Verified date |
April 2022 |
| Source |
VA Office of Research and Development |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial 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.
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.
