Application of the Modified Story Memory Technique (mSMT)© to Aging



Status:Recruiting
Conditions:Cognitive Studies, Cognitive Studies, Healthy Studies
Therapuetic Areas:Psychiatry / Psychology, Other
Healthy:No
Age Range:65 - Any
Updated:12/14/2017
Start Date:November 1, 2017
End Date:November 1, 2021
Contact:Nancy B Moore, MA
Email:nbmoore@kesslerfoundation.org
Phone:973-324-8450

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This study is a double-blind placebo-controlled randomized clinical trial (RCT) to provide
Class I evidence in support of or in refute of the efficacy of the modified Story Memory
Technique (mSMT) in healthy aging (HA)and in persons with mild cognitive impairment (MCI).
Outcomes will be measured through three mechanisms: (1) a traditional neuropsychological
evaluation (NPE) (2) an assessment of global functioning (AGF) examining the impact of the
treatment on daily activities, and (3) an optional functional magnetic resonance imaging
(fMRI) scan.

Studies conducted at Kessler Foundation (KF) have demonstrated the modified Story Memory
Technique (mSMT) to be effective for improving new learning in individuals with MS and TBI.
Efficacy of the individualized mSMT has been clearly demonstrated across three realms of
functioning, objective behavior, brain functioning and everyday life in multiple RCTs with
both MS and TBI samples. This convincing data provides Class I evidence supporting the
efficacy of the individual mSMT for improving new learning and memory in MS with
documentation of long-lasting treatment effects on both standardized learning tests and
neuroimaging. Current work with the mSMT is focusing on a group administration format, with a
RCT funded by the Department of Defense.

Ongoing work in healthy aging (HA), led by George Rebok, PhD at the Johns Hopkins School of
Public Health, has applied cognitive retraining to older healthy adults. Multiple, strong
rationale for pursuing such applications of cognitive rehabilitation include the fact that
the 65 and older population is growing (an estimated 20% of population (72 million) will be
65 and older by 2030), cognitive decline is most feared aspect of growing older, drug trial
results addressing this challenge have been disappointing and, most importantly, cognitive
impairments heavily affect the aging population. Specifically, 1 in 4 adults 70 years or
older have a cognitive impairment without dementia and roughly 5.3 million people in the U.S.
have Alzheimer's disease. Rebok and colleagues have applied Speed of Processing Training to a
large cohort of healthy older adults (age 65+) and found a 33-48% risk reduction of dementia
onset 10 years post treatment. These encouraging results suggest that providing cognitively
enhancing treatments prior to the onset of dementia may in fact stave off the dementia
process and provide older individuals with more years free of cognitive deficit.

Given the substantial success of the mSMT in improving new learning and memory functioning in
persons with TBI and MS, we seek to apply the mSMT to an aging population with multiple aims.

Aim 1. Examine the efficacy of the mSMT to increase learning and memory abilities in older
adults with mild cognitive impairment (MCI) and older adults with no signs of cognitive
impairment (healthy aging group: HA).

Aim 2. Examine the long term impact of the mSMT on new learning and memory abilities one and
two years post-intervention for both the MCI group and the HA group.

Aim 3. Examine the impact of early cognitive enhancement with the mSMT on measures of daily
life functioning and overall quality of life immediately posttreatment and at each follow-up
assessment.

Aim 4. Examine the neural correlates during encoding and retrieval associated with early
cognitive enhancement from the mSMT immediately post-treatment and at each follow-up
assessment

To achieve these goals, we will recruit 40 individuals over the age of 65 to participate in
the study. Each participant will undergo baseline cognitive assessment. Based on the
assessment results, he / she will be allocated to the HA block or the MCI block. Within each
block, participants will be randomized to a treatment group or a placebo control group. The
treatment group will undergo 10 sessions of the mSMT, while the placebo control group will
undergo 10 sessions of memory exercises. We have used this placebo condition in multiple
randomized clinical trials in the past, with success. Repeat assessments will then occur
within one week of completing treatment, 6 months after completing treatment, one year after
completing treatment and 2 years after completing treatment. Each assessment will evaluate
new learning and memory abilities as well as multiple other aspects of cognitive functioning
through a neuropsychological assessment (NP). Participants will also complete an assessment
of global functioning (AGF) which evaluates cognitive functioning in daily life. In addition,
we will collect neuroimaging data on a subsample of participants willing and able to complete
imaging procedures

Inclusion Criteria:

- older than 65

- primary language is English.

Exclusion Criteria:

- diagnosis of any neurological condition (Alzheimer's disease, dementia, stroke,
multiple sclerosis, Brain Injury, Parkinson's disease, etc.).

- diagnosis of a psychiatric disorder such as post-traumatic stress disorder,
schizophrenia or bipolar disorder.

- abuse of illicit drug within the past 6 months.

For optional MRI

- pacemaker or other implanted electrical device, brain stimulator, aneurysm clip (metal
clips on the wall of a large artery), metallic prostheses (including metal pins and
rods, heart valves, and internal hearing aids [cochlear implants]), permanent
eyeliner, implanted delivery pumps, or shrapnel fragments.

- dental implants

- left handed.
We found this trial at
1
site
120 Eagle Rock Avenue
East Hanover, New Jersey 07936
Phone: 973-324-8450
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East Hanover, NJ
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