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Active, not recruiting Not applicable

Magnetic Resonance Imaging (MRI) and Eye-tracking Predictive Markers of Cognitive Ageing.

NCT06058897 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2024-03-22
Last updated
2026-07-16

Condition(s) studied

Aging

Investigational drug(s) / intervention(s)

MRIeye-trackingcognitive exams

MRI: MRI examinations will be conducted on the 3T MRI technical platform. During the MRI examination, images reflecting the integrity of the LC (quantification of neuromelanin as well as its functional connections with the different brain regions (resting functional MRI) will be acquired. High-resolution T1 and T2 weighted images of the the entire brain will also be acquired for the volumetry of cerebral areas.

eye-tracking: Eye tracking examinations will be conducted using an EyeBrain medical device (class IIa) developed by Suricog. This eye tracker will be installed in a box, in an experimental room. The eye tracker is combined with a computer to present visual cognitive tasks. Pupillary dilation/constriction measurements will be acquired at rest (when fixing a cross presented on the screen) and during the performance of different cognitive tasks (exploration and processing of scenes visuals, reading texts, making saccades or anti-saccades when presenting visual targets). These pupillary measurements will then be linked to the memorization of the stimuli presented, this recognition being tested at the end of the exam.

cognitive exams: Cognitive measures will be acquired during an evaluation session through interactive cognitive exercises. These exercises are developed using tools offered by Covirtua Healthcare (Covirtua Cognition software). Some exercises will test cognitive systems a priori dependent on NA release (episodic memory, working memory, selective attention, selective inhibition, planning) and other a priori independent of NA (semantic memory: categorization, naming).

Study summary

This research proposes to investigate physiological and cognitive markers of locus coeruleus (LC) neuronal integrity and function in cognitively-healthy participants over 60 years old. The locus coeruleus is a brainstem nucleus, sole source of noradrenaline for the brain. Tau pathology appears in neurons of this nucleus, which may induce initial cognitive changes. The study aims at relating locus coeruleus markers, assessed with MRI and eye-tracking techniques, with cognitive function.

Eligibility

Sex
ALL
Min age
60 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * INSPIRE cohort participant * Mini-Mental State Examination score ≥ 27 on 30 * Access to a web connection from participant's or relative's home and regular use of web surfing * Signature of the informed consent * Affiliated to a social security scheme Exclusion Criteria: * Any contra-indications to MRI exam * Ophthalmic pathology impacting eye-tracking measures * Neurological or psychiatric pathology * Person under guardianship or curatorship Contraindications to MRI examination: * Pacemaker or cardiac defibrillator * Implanted material activated by an electrical, magnetic or mechanical system * Haemostatic clips for intracerebral aneurysms or carotid arteries * Orthopedic implants * Claustrophobia Ophthalmological pathologies impacting eye tracking measurements: * Glaucoma * Age-related macular degeneration * Unoperated cataract

Primary outcome measure(s)

  • Imaging contrast between the LC nucleus and the pontine tegmentum region — 18 months
    The outcome will be measured with brainstem anatomical MRI (no unit) at visits V1 (immediately after inclusion) and V4 (18 months after inclusion).

Trial sites (1)

FacilityCityRegionStatus
University Hospital Toulouse France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06058897 on ClinicalTrials.gov ↗ ← All trials in France