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临床试验/NCT06963879
NCT06963879Enrolling By Invitation不适用

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

Braingaze1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
60
试验地点
1
主要终点
Beta biomarkers

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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.

排除标准

  • •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.

研究组 & 干预措施

BGaze Therapy MCI

Experimental

30 Patients with Mild Cognitive Impairment for validation and 15 for therapy

干预措施: Bgaze Therapy (Device)

BGaze Therapy MCI

Experimental

30 Patients with Mild Cognitive Impairment for validation and 15 for therapy

干预措施: Bgaze Attention Task (Diagnostic Test)

BGaze Therapy AD

Experimental

30 Patients with Early Alzheimer's Disease for validation and 15 for therapy

干预措施: Bgaze Therapy (Device)

BGaze Therapy AD

Experimental

30 Patients with Early Alzheimer's Disease for validation and 15 for therapy

干预措施: Bgaze Attention Task (Diagnostic Test)

结局指标

主要结局

Beta biomarkers

时间窗: Immediately after the intervention

Measure changes in plasma ßA40 and ßA42 in pg/mL

PTau Biomarkers

时间窗: Immediately after the intervention

Measure changes in plasma PTau181 and pTau217 in pg/mL

Pupil Response

时间窗: Immediately after the intervention

Pupillary diameter in millimeters (mm) will be calculated from data obtained using eye-tracking devices.

Ocular vergence

时间窗: Immediately after the intervention

Ocular vergence in degrees (°) will be calculated from data obtained using eye-tracking devices.

次要结局

  • Montreal Cognitive Assessment (MoCA) Score(Immediately after the intervention)

研究者

发起方
Braingaze
申办方类型
Industry
责任方
Principal Investigator
主要研究者

Hans Supèr

Principal Investigator

Braingaze

研究点 (1)

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