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Multimodal Assesment of Alzheimer Patients

Multimodal Assessment of Cognitive Impairment in Alzheimer Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06448403
Acronym
MultiAD
Enrollment
60
Registered
2024-06-07
Start date
2024-07-01
Completion date
2030-12-29
Last updated
2025-08-07

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

Conditions

Mild Cognitive Impairment, Alzheimer Disease, Late Onset, Cognitive Impairment, Dementia

Keywords

Alzheimer Disease (AD), Mild cognitive impairment (MCI), Brain Diseases, Nervous System Disorders, Neurodegenerative Diseases, Dementia, Cognitive impairment

Brief summary

The goal of this study is to learn more about the changes in the brains of patients with cognitive impairment (MCI) and Alzheimer's Disease (AD). The main questions the study aims to answer are: 1. What findings can be used to earlier detect patients that will develop Alzheimers? 2. Which differences are seen between healthy and cognitively impaired patients? 3. Which differences are seen between patients with Alzheimers disease? Participants will undergo: * Cognitive tests * Magnetic resonance imaging (MRI) * Electroencephalography (EEG) * Blood sample collection * Fecal sample collection * A randomized group will undergo polysomnography analysis.

Detailed description

The projects aims to map brain changes in patients with mild cognitive impairment (MCI) and Alzheimer's Disease (AD) by combining different assesment modalities. In the MRI, researchers will get the opportunity to analyse both structural and functional brain changes. In the EEG, changes in elctrical activites will be measured. The blood samples allow researchers to analyse specific dementia and inflammation proteins, while fecal speciments can be used to assess bacterial composition. Additionally, the cognitive testing allow to assess the specific part of cognitive function which is affected.

Interventions

BIOLOGICALFecal samples

Analysis of bacterial composition.

MRI scanning with volumetric, resting and activity-based sequences.

DEVICE64-channel EEG

EEG to quantifiy electric activity.

DEVICEPolysomnography

A randomized group will undergo polysomnography.

BIOLOGICALBlood samples

Analysis of specific blood biomarkers.

BEHAVIORALCognitive tests

Interview-based cognitive tests for assesment of cognitive levels.

Sponsors

Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* MCI and AD according to relevant ICD-criterias. * Control cohort is age and gender matched with other cohorts.

Exclusion criteria

* Uneligibility for any of the planned neuroimagery devices (MRI, EEG) * AD diagnosis before the age of 65 (Early-onset AD). * Brain tumor * Traumtic head injury * Earlier neurosurgery * Other neyrodegenerative diseases (i.e Parkinson and ALS) * Diseases related to inflammation and auto-immunity (i.e MS)

Design outcomes

Primary

MeasureTime frameDescription
MCI-AD converters5 yearsIdentify biomarker profiles unique for patients with MCI that develop AD for earlier prediction.
AD-subclassification5 yearsIdentify biomarker profiles that can assist in a more thorough AD-classification

Countries

Norway

Contacts

Primary ContactAxel Sandvig, Prof., MD, PhD
axel.sandvig@ntnu.no72 57 56 20

Outcome results

None listed

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