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Neuroelectrical Biomarkers for Alzheimer's Disease Stages

NEw approacheS for The dIagnosis of AlzeiMer's diseAse Through neuroElectrical Changes in the Brain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01880151
Acronym
ESTIMATE
Enrollment
87
Registered
2013-06-18
Start date
2013-07-12
Completion date
2019-01-31
Last updated
2021-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease

Keywords

Alzheimer's disease, Dementia, Prodromal, EEG, ERP, Biomarkers

Brief summary

Recent diagnostic criteria for Alzheimer's disease (AD) recognize an extended spectrum of AD stages as part of the disease, including a preclinical stage. This underscores the importance of early prognosis of AD when it is still possible to influence the course of the disorder. The investigators propose a comprehensive project which will target the data-driven modeling of the disease development. This goal will be achieved by creating and validating a battery of new sensitive biomarkers for clinical evaluation and prediction of AD in individuals. The AD-related brain changes will be assessed by noninvasive functional EEG measured during an episodic memory task in subjects at different stages of AD, as well as in healthy controls. The novel functional biomarkers will be extracted using a rigorous multistage selection procedure involving advanced methods for feature extraction, as well as statistics and classification for optimal selection. The ESTIMATE project will serve as a first step in an extensive array of research procedures which will enable the early clinical identification of Alzheimer's disease in elderly individuals who could then take advantage of preventive pharmaceutical therapies.

Interventions

DEVICEEEG

EEG recorded during a resting condition and during an episodic memory task condition

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
70 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Age: 70-85 years old * Presence of memory impairment * Completed educational level: middle school * Visual and auditory acuity: normal or corrected-to-normal

Exclusion criteria

* Monogenic AD * Presence of a neurological disorder * Stroke that has occurred in the last three months * Prohibited medications * Residence in skilled nursing facility * Illiteracy, is unable to count or to read * Claustrophobia

Design outcomes

Primary

MeasureTime frame
Frequency band charactersitics of the electrophysiological brain responseBaseline

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026