Huntington Disease
Conditions
Keywords
video oculography
Brief summary
The purpose of this study is to know the limits of feasibility of a reliable oculomotor record for patient with Huntington's disease.
Interventions
DEVICEEye-tracking
Sponsors
University Hospital, Angers
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Corrected visual acuity \>1/10 * Aged over 18 years * Patient with the mutation that is to say the presence of an abnormal number of trinuclide: CAG\> 38 in the first exon of the huntingtin gene. * Total Functional Capacity Scale (CFT) ≥ 3
Exclusion criteria
* Patients or trustworthy person who have not given their written consent, informed and signed. * Patients are not affiliated or who are not entitled to Social Security * Private patients of liberty by administrative or judicial decision, or patients supervision * Associated disease with neurological repercussions
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| saccadic measures with the eye tracker | 1 day | one measure in the evening and one in the afternoon |
Countries
France
Contacts
Primary ContactSophie Hue
Outcome results
None listed