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Eye-tracking parameters as biomarkers of frontotemporal dementia

Eye-tracking parameters as biomarkers of frontotemporal dementia - Eye-tracking in FTD (FTDEYE)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON51509
Enrollment
136
Registered
2022-10-28
Start date
2022-10-31
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Alzheimer's disease Frontotemporal dementia

Interventions

None listed

Sponsors

Neurologie
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) Patients with FTD referred to our referral center and diagnosed with use of International Consensus Criteria. The dementia symptoms have to be mild (clinical dementia rating

Exclusion criteria

Exclusion criteria: Subjects with a previous stroke or other (neurological) conditions that may affect cognitive functions (brain tumour, multiple sclerosis, use of psycho-active medications) will be excluded from participation in this study.

Design outcomes

Primary

MeasureTime frame
Eye movement features derived from the eye-tracking test battery.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)