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Validation Study of a New Digital Diagnostic and Treatment Test Based on Interactive Video Games for Alzheimer's Disease

Validation Study of a New Digital Diagnostic and Treatment Test Based on Interactive Video Games for Alzheimer's Disease

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06963879
Acronym
EyeAD
Enrollment
60
Registered
2025-05-09
Start date
2025-05-01
Completion date
2025-12-31
Last updated
2025-05-09

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

Conditions

Alzheimer Disease, MCI

Brief summary

This study aims to validate a novel, non-invasive diagnostic and digital therapeutic approach for Alzheimer's Disease (AD), centered on an interactive video game called BGaze Therapy. This platform leverages eye-tracking technology to assess and potentially enhance cognitive functions, particularly attention and memory. The diagnostic component of the study investigates the use of eye vergence responses-elicited during a visual attention task-as potential biomarkers for early AD. Specifically, the study will re-validate eye vergence by comparing response patterns among three groups: cognitively healthy older adults, individuals with Mild Cognitive Impairment (MCI), and patients with confirmed AD, based on blood biomarkers (ßA40, ßA42, pTau181, and pTau217). The diagnostic task follows an oddball paradigm, where participants must detect target images (grapes) among distractors (other fruits) across 100 one-second trials, lasting approximately three minutes. Eye vergence is recorded using remote infrared eye-tracking, while participants simply fixate on a computer screen. The therapeutic aspect evaluates the impact of BGaze Therapy, which employs serious games designed to train attentional control through eye movements. The game dynamically adjusts its difficulty in real time and provides continuous feedback to enhance user engagement and learning efficacy. Participants will undergo pre-testing-including blood biomarker analysis and standardized cognitive assessments (MMSE and MoCA)-followed by a two-month training phase at care centers using the BGaze Therapy system. Post-intervention testing will mirror the pre-test protocol to assess cognitive and neurological changes. A total of 60 participants (30 with MCI and 30 with AD) will be recruited for the validation phase. A subsample (15 MCI and 15 AD participants) will be selected for the treatment phase. Ultimately, this study aims to establish BGaze as a cost-effective, scalable, and non-invasive tool for the early diagnosis and treatment of Alzheimer's Disease by addressing the attentional and cognitive deficits associated with the condition.

Interventions

DEVICEBgaze Therapy

BGaze Therapy is a digital intervention by Braingaze designed to enhance attention and memory in individuals with Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI). It uses an interactive video game controlled through eye-tracking, allowing users to play using only their gaze. The therapy is based on research linking eye vergence and pupil responses to cognitive processing-physiological markers that may indicate neurodegeneration. During gameplay, these responses are modulated, potentially inducing gamma brain oscillations associated with reduced AD pathology. Patients play at care-center for 5-10 minutes daily over two months. Equipment is provided, and both in-person and remote support ensure usability. The game adapts difficulty in real time and provides feedback to keep users engaged and stimulate cognitive function.

DIAGNOSTIC_TESTBgaze Attention Task

For the validation of diagnosis of AD with vergence method the Attention Test (B-Gaze) will be used. This is an odd ball paradigm where visual target has to be detected among blue distractors. The test consist of 100 trials of 1 second and last about 3 minutes. The task uses remote eye infra-red tracking to measure eye vergence. Subjects merely have to fixate at the computer screen during the task.

Sponsors

Braingaze
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 50 years or older. * Clinical diagnosis of early-stage AD or MCI based the criteria of National Institute on Aging-Alzheimer's Association. * Capable of providing informed consent.

Exclusion criteria

* Severe cognitive impairment (MMSE \< 10). * Neurological conditions affecting cognition (e.g., stroke). * Severe psychiatric disorders. * Structural brain abnormalities (e.g., tumors) with cognitive impact. * Significant visual impairments. * Inability to understand or communicate in Spanish.

Design outcomes

Primary

MeasureTime frameDescription
Beta biomarkersImmediately after the interventionMeasure changes in plasma ßA40 and ßA42 in pg/mL
PTau BiomarkersImmediately after the interventionMeasure changes in plasma PTau181 and pTau217 in pg/mL
Pupil ResponseImmediately after the interventionPupillary diameter in millimeters (mm) will be calculated from data obtained using eye-tracking devices.
Ocular vergenceImmediately after the interventionOcular vergence in degrees (°) will be calculated from data obtained using eye-tracking devices.

Secondary

MeasureTime frameDescription
Montreal Cognitive Assessment (MoCA) ScoreImmediately after the interventionScore in the Montreal Cognitive Assessment (MoCA); units on a scale (0-30), with higher scores indicating better cognitive function.

Countries

Spain

Outcome results

None listed

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