Feasibility of a Video-oculography in Patients With Huntington's Disease VOG-HD Study
Not Applicable
- Conditions
- Huntington Disease
- Interventions
- Device: Eye-tracking
- Registration Number
- NCT02563418
- Lead Sponsor
- University Hospital, Angers
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 60
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Patient with Huntington's disease Eye-tracking -
- Primary Outcome Measures
Name Time Method saccadic measures with the eye tracker 1 day one measure in the evening and one in the afternoon
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Centre Hospitalier Universitaire
🇫🇷Angers, France