Development and Validation of a Novel Functional Eye-Tracking Software Application for Alzheimer's Disease
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Alzheimer's Disease
- Sponsor
- Innodem Neurosciences
- Enrollment
- 250
- Locations
- 1
- Primary Endpoint
- Clinical Dementia Rating (CDR) score, one time, at the day of enrollment.
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
This study aims to develop and validate a sensitive and non-invasive eye-tracking software application.
This study will obtain participant responses to brief cognitive tests designed to evaluate several key functions known to be affected by Alzheimer's Disease and non-invasive eye movement measurements in response to visually presented stimuli during specifically designed eye-tracking tests. The study data will be used to develop machine learning algorithms and validate a software application intended to track the progressive component of Alzheimer's Disease and associated cognitive changes.
Investigators
Eligibility Criteria
Inclusion Criteria
- •For all participants:
- •Able to provide informed consent
- •Aged 18 years or older at the time of enrollment
- •Able to read in either French or English
- •Visual acuity of 20/100 in at least one eye (corrective glasses, contact lenses, surgery etc. are permitted)
- •For patients only:
- •Confirmed diagnosis of AD based on the NIAAA diagnostic criteria of probable AD
- •Having undergone a full neuropsychological evaluation within the last 6 months or having a planned full neuropsychological evaluation within the next 6 months.
- •AD diagnoses supported by FDG-PET scan or amyloid biomarkers (CSF or amyloid PET)
Exclusion Criteria
- •For AD participants:
- •Diagnosed with one of the following dementia subtypes: Fronto-temporal dementia, Lewy-body dementia, or Creutzfeldt-Jakob disease.
- •Incapacity to provide informed consent or inability to adequately understand the task instructions.
- •For all participants:
- •Evidence or medical history of psychiatric issues, which are known to also affect movements and oculomotor control.
- •Presence of comorbid neurological conditions to avoid eye movement anomaly confounds (strabismus, cranial nerve palsy, stroke-causing hemianopsia).
- •Diagnosis of macular edema or other pre-existing ocular conditions (e.g., glaucoma, cataracts) that would prevent from performing the eye movement assessments.
- •Unstable medication use: recent (less than one month from enrollment) start of, change of dose, or irregular use of, new prescription drugs known to have an effect on ocular motor visual function, such as benzodiazepines, antipsychotics and anticonvulsants. Occasional use of benzodiazepines for medical procedures is permitted, at the investigator's discretion, but should not occur within a short time period of an eye movement assessment.
- •Diagnosed with an active substance use disorder.
- •History of stroke.
Outcomes
Primary Outcomes
Clinical Dementia Rating (CDR) score, one time, at the day of enrollment.
Time Frame: Baseline
The Clinical Dementia Rating (CDR) is a global rating scale for staging patients diagnosed with Alzheimer disease and other dementias and monitoring changes in the level of there disabilities over time. The CDR scale is a 0-3 point numeric scale (0.5 unit increments) derived from clinician rating of cognition and daily function in the domains of memory, orientation, judgment and problem solving, community affairs, home and hobbies and personal care.
Secondary Outcomes
- The Montreal Cognitive Assessment (MoCA) score, one time, at the day of enrollment.(Baseline)
- The Mini-Mental State Exam (MMSE) score, one time, at the day of enrollment.(Baseline)