Actively Recruiting

Age: 65Years +
All Genders
Healthy Volunteers
ID06448403

Multimodal Assessment of Cognitive Impairment in Alzheimer Patients

Led by Norwegian University of Science and Technology · Updated on 2025-08-07

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying brain changes in people aged 65 and older with mild cognitive impairment (MCI) and Alzheimer's disease (AD). The study aims to identify early signs that predict who will develop Alzheimer's, compare brain differences between healthy individuals and those with cognitive impairment, and distinguish variations among Alzheimer's patients. This observational research combines multiple methods to better understand these conditions. Participants will undergo several assessments including cognitive tests to evaluate brain function, magnetic resonance imaging (MRI) to examine structural and functional brain changes, and 64-channel electroencephalography (EEG) to measure brain electrical activity. Blood and fecal samples will be collected to analyze dementia-related proteins and gut bacterial composition. Additionally, a randomized subset of participants will have polysomnography to assess sleep patterns. Throughout the study, participants will be evaluated using cognitive interviews, neuroimaging scans, and biological sample analyses to monitor changes over time. The main outcomes tracked over five years include conversion from MCI to Alzheimer's and subtypes of Alzheimer's disease. The study involves healthy volunteers and includes control groups matched by age and gender, with ongoing monitoring by the Norwegian University of Science and Technology.

CONDITIONS

Brief Title

Multimodal Assesment of Alzheimer Patients

Who Can Participate

Age: 65Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of mild cognitive impairment (MCI) or Alzheimer's disease (AD) according to relevant ICD criteria
  • Control participants matched by age and gender with MCI and AD groups
  • Age 65 years or older
Not Eligible

You will not qualify if you...

  • Unable to undergo planned neuroimaging tests such as MRI or EEG
  • Diagnosis of Alzheimer's disease before age 65 (early-onset AD)
  • Presence of brain tumor
  • History of traumatic head injury
  • Previous brain surgery
  • Other neurodegenerative diseases like Parkinson's disease or ALS
  • Diseases related to inflammation or auto-immunity such as multiple sclerosis (MS)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo MRI scanning, EEG, cognitive tests, and biological sample collection to assess brain changes and cognitive function.

1 to 2 visits depending on assessments

Long-term Monitoring

Duration - Up to 5 years

Participants are observed over time to monitor cognitive status and disease progression.

Annual visits for up to 5 years

Trial Site Locations

Total: 1 location

1

Norwegian University of Sciene and Technology / Norges teknisk-naturvitenskapelige universitet (NTNU)

Trondheim, Trønderlag, Norway, 7030

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Research Team

A

Axel Sandvig, Prof., MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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