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Spatial Navigation for the Early Detection of Alzheimer's Disease.

Not Applicable
Recruiting
Conditions
Alzheimer Disease
Healthy Aging
Mild Cognitive Impairment
Interventions
Diagnostic Test: Procedure for patients
Diagnostic Test: Procedure for healthy controls
Registration Number
NCT06385951
Lead Sponsor
University Hospital, Ghent
Brief Summary

Alzheimer's Disease (AD) is the most common form of dementia and may contribute to 60-70 % of all cases. An early, accurate diagnosis of AD will become increasingly important with disease-modifying therapies. Different types of fluid and neuroimaging biomarkers are available for the early detection of AD. However, implementation of routine use of these biomarkers in clinical settings is held back due to the risk of overdiagnosis, increased cost and invasiveness of the assessment method. Therefore, novel biomarkers are needed beyond the amyloid and tau pathologies for the early diagnosis of AD. Neuropsychological paper and pencil tests can detect AD and discriminate between different clinical stages. Since medial temporal lobe structures, including the hippocampus and entorhinal cortex (EC), are involved in spatial navigation and degenerate in the earliest stages of AD, spatial navigation can be considered as an early cognitive biomarker of the disease. Nonetheless, the measurement of spatial navigation needs further improvement since the current paper and pencil tests lack ecological validity. Therefore, the test environment should be set up in immersive Virtual Reality (iVR). Dr. Andrea Castegnaro (Space and Memory Lab of University College of London) developed the Allocentric Spatial Update Task (ALLO task), which is an iVR task measuring egocentric and allocentric spatial abilities.

Therefore, the main objective of this study is to evaluate whether allocentric and egocentric spatial navigation, measured by the ALLO iVR task can be considered a cognitive biomarker for the early detection of AD. In addition, the investigators want to report on the neuronal correlates of both spatial navigation strategies.

Through the Department of Neurology of the University Hospital of Ghent, which has a large cognitive disorders clinic, patients with mild cognitive impairment and mild Alzheimer's dementia will be recruited. Participants will undergo standard clinical assessment, including a neuropsychological examination, Magnetic Resonance Imaging, a 18F-fluorodeoxyglucose PET and a Lumbar Puncture. In addition, participants will also be asked to undergo Tau PET imaging, Amyloid PET imaging and complete the ALLO iVR task. Healthy controls will also be recruited and have to undergo the same investigations, except for the amyloid PET and lumbar puncture.

Detailed Description

Alzheimer's Disease (AD) is the most common form of dementia and may contribute to 60-70 % of all cases. It can be presented as a spectrum of progressive cognitive decline, with early episodic memory impairment, followed by progressive deterioration of other cognitive functions such as praxis, visual processing and spatial navigation. An early, accurate diagnosis of AD will become increasingly important with disease-modifying therapies. Different types of fluid and neuroimaging biomarkers are available for the early detection of AD. However, implementation of routine use of these biomarkers in clinical settings is held back due to the risk of overdiagnosis, increased cost and invasiveness of the assessment method. Therefore, novel biomarkers are needed beyond the amyloid and tau pathologies for the early diagnosis of AD.

Neuropsychological paper and pencil tests can detect AD and discriminate between different clinical stages. Traditionally, early episodic memory impairment has been considered the most specific cognitive biomarker of early AD. However, since medial temporal lobe structures, including the hippocampus and entorhinal cortex (EC), are involved in spatial navigation and degenerate in the earliest stages of AD, spatial navigation can also be considered as an early cognitive biomarker of the disease. Nonetheless, the measurement of spatial navigation needs further improvement since the current paper and pencil tests lack ecological validity. Therefore, we should evolve to a more innovative way of spatial navigation assessment that is more in line with the real world and set up the test environment in immersive Virtual Reality (iVR). Dr. Andrea Castegnaro (Space and Memory Lab of University College of London) developed the Allocentric Spatial Update Task (ALLO task), which is an iVR task measuring egocentric and allocentric spatial abilities.

Therefore, the main objective of this study is to evaluate whether allocentric and egocentric spatial navigation, measured by the ALLO iVR task can be considered a cognitive biomarker for the early detection of AD. In addition, the investigators want to report on the neuronal correlates of both spatial navigation strategies.

Through the Department of Neurology of the University Hospital of Ghent, which has a large cognitive disorders clinic, patients with mild cognitive impairment and mild Alzheimer's dementia will be recruited. Participants will undergo standard clinical assessment, including a neuropsychological examination, Magnetic Resonance Imaging, a 18F-fluorodeoxyglucose PET and a Lumbar Puncture. In addition, participants will also be asked to undergo Tau PET imaging, Amyloid PET imaging and complete the ALLO iVR task. Healthy controls will also be recruited and have to undergo the same investigations, except for the amyloid PET and lumbar puncture.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
160
Inclusion Criteria
  • Patients with a Mild Cognitive Impairment (MCI) due to Alzheimer's Disease (AD)
  • Patients with a mild Alzheimer's Dementia
  • Patients with MCI without a formal dementia diagnosis
  • Healthy controls
Exclusion Criteria
  • Diabetes (only for healthy controls)
  • Epilepsy
  • Presence of extreme depressive symptoms (>11 on Geriatric depression scale or >20 on Beck depression inventory)
  • Presence of extreme anxiety (>22 on Beck Anxiety Inventory)
  • A major psychiatric of medical disorder
  • Alcohol excess
  • Moderate to severe white matter lesions on MRI (>2 Fazekas)
  • Any visual of mobility impairment of such severity as to compromise the ability to undertake the iVR task.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PatientsProcedure for patientsPatients with mild cognitive impairment and mild Alzheimer's dementia
Healthy volunteersProcedure for healthy controlsHealthy volunteers
Primary Outcome Measures
NameTimeMethod
Spatial navigation abilities1 hour

Spatial navigation abilities (egocentric and allocentric) will be measured by means of the ALLO iVR task.

Secondary Outcome Measures
NameTimeMethod
Medial Temporal Lobe atrophy20 minutes

MRI

Amount and spreading of tau in the brain1 hour

Tau-PET

amyloidB1-42 / 40 ratio, total tau and phosphorylated tau1 hour

Lumbar puncture

Cognitive functioning1.5 hours

Neuropsychologische examination

Amount and spreading of amyloid in the brain1 hour

Amyloid PET

Decreases in cerebral glucose metabolism in the brain1 hour

FDG-PET

Trial Locations

Locations (1)

University Hospital Gent

🇧🇪

Ghent, East-Flanders, Belgium

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