Evolution of Memory Related Activity
Recruitment status was Recruiting
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Purpose
The purpose of this study is to begin the process of validating fMRI (functional magnetic resonance imaging) as a biomarker for use in clinical trials and longitudinal studies of clinical progression in mild cognitive impairment (MCI) and Alzheimer's disease (AD).
| Condition |
|---|
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Alzheimer's Disease Mild Cognitive Impairment |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Cross-Sectional |
| Official Title: | Evolution of Memory-related fMRI Activation Over the Course of MCI and AD |
| Estimated Enrollment: | 160 |
| Study Start Date: | May 2006 |
| Estimated Study Completion Date: | May 2011 |
| Estimated Primary Completion Date: | May 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
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NC
Normal older controls, not cognitively impaired; MMSE 27-30 and performance above education adjusted cutoff scores on the Logical Memory II subscale (LM-II Delayed Paragraph Recall) of the Wechsler Memory Scale
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vMCI
Very mild cognitive impairment; less severe objective memory deficit, scoring .5 to 1.5 S.D. (standard deviation) below education adjusted norms on the LM-II
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sMCI
significant mild cognitive impairment; objective cut off of 1.5 S.D. level below education adjusted norms on the LM-II
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AD
Mild Alzheimer's disease; meet NINCDS/ADRDA criteria for probable AD with mild dementia severity (CDR Total = 1), MMSE 20-26
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Detailed Description:
The development of biomarkers is now especially critical, as there are a number of promising disease-modifying therapies entering early phase clinical trials, with additional novel therapeutic strategies in development. It is essential to develop biomarkers that can detect a "signal of efficacy" over a relatively short time frame for use in Phase II trials. Ideally biomarkers are needed that can reliably detect the earliest brain alterations due to AD pathology, perhaps at a point when there is synaptic dysfunction but not yet widespread neuronal loss. Functional neuroimaging, in particular functional MRI (fMRI), has significant potential, having already shown promise in detecting regionally specific pharmacological effects on memory related neural activity, and as a sensitive marker of very early cognitive impairment.
This study, a parallel ancillary study of the Alzheimer's Disease Neuroimaging Initiative (ADNI), will first examine reproducibility of fMRI activation, using a face-name associative memory paradigm, and then the alterations in memory-related activation that occur over the course of MCI and mild AD. The study will also examine the relationship of fMRI activation to clinical variables, memory task performance, genotype, and other imaging techniques cross-sectionally and longitudinally, sampling at multiple time points over a 3-year period.
Eligibility| Ages Eligible for Study: | 55 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Memory Disorders Unit at Brigham and Women's Hospital, the Gerontology Research Unit at Massachusetts General Hospital, Alzheimer's Association, area physicians, and community dwelling adults
Inclusion Criteria:
- Ages 55-90
- General good health or stable medical problems
- Study partner/caregiver able to provide an independent evaluation of the participant's daily functioning
- No contraindications to MR scanning
- Modified Hachinski Ischemic Score ≤4
- Geriatric Depression Scale ≤10
Exclusion Criteria:
- Diagnosis of Parkinson's disease or other neurological illness
- Presence of clinically significant/uncontrolled medical conditions
- History of stroke, brain tumor, brain surgery, seizures, significant head trauma with loss of consciousness, depression or other psychiatric illness, alcohol or drug abuse in the past 2 years
- Significant uncorrectable visual impairment
Contacts and Locations| Contact: Caroline Sullivan | 617-726-6212 | csullivan21@partners.org |
| Contact: Meghan Frey | 617-732-8085 | mfrey1@partners.org |
| United States, Massachusetts | |
| Brigham and Women's Hospital | Recruiting |
| Boston, Massachusetts, United States, 02115 | |
| Contact: Meghan Frey 617-732-8085 mfrey1@partners.org | |
| Massachusetts General Hospital | Recruiting |
| Boston, Massachusetts, United States, 02129 | |
| Contact: Caroline Sullivan 617-726-6212 csullivan21@partners.org | |
| Principal Investigator: | Reisa Sperling, MD | Director of Clinical Research, Memory Disorders Unit, Brigham and Women's Hospital |
More Information
Publications:
| Responsible Party: | Reisa A. Sperling, MD, Brigham and Women's Hospital |
| ClinicalTrials.gov Identifier: | NCT00902499 History of Changes |
| Other Study ID Numbers: | IA0159, 5R01AG027435-04 |
| Study First Received: | May 13, 2009 |
| Last Updated: | July 23, 2010 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute on Aging (NIA):
|
functional magnetic resonance imaging |
Additional relevant MeSH terms:
|
Alzheimer Disease Cognition Disorders Dementia Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Tauopathies Neurodegenerative Diseases Delirium, Dementia, Amnestic, Cognitive Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 19, 2013