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Study of Eye Movements (EYE) as Early Markers of Brain Dysfunction (BRAIN) in Parkinson's Disease (PARK)

Study of Eye Movements (EYE) as Early Markers of Brain Dysfunction (BRAIN) in Parkinson's Disease (PARK)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04212637
Acronym
eyebrainpark
Enrollment
80
Registered
2019-12-27
Start date
2021-01-31
Completion date
2022-01-31
Last updated
2020-11-17

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

Conditions

Parkinson Disease

Brief summary

Identify the neural bases of eye movements during visual tasks and their dysfunction at early stages of Parkinson disease (de novo).

Interventions

OTHERMRI

Examine BOLD activity in relation to eye movements measures

Sponsors

Laboratoire de Psychologie et NeuroCognition
CollaboratorOTHER
University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

for all: * Visual acuity normal or corrected to normal * Affiliation to a social security scheme (copy of the vital card in support) * Signed informed consent * Medical examination according to the participation in the MRI examination * MMSE score\> 23/30 For Parkinson patient: * Diagnosis of Parkinson's disease * Presence of asymmetric bradykinesia and rest tremor and / or stiffness * Hoehn & Yahr Stadium I-II / V

Exclusion criteria

for all: * Unprotected Majors unable to express their consent * Protected Major (Persons mentioned in Articles L1121-5,6 and 8 of the public health code) * Significant hearing or motor impairment * Past or present neuropsychiatric pathology (except benign epilepsy) * Taking narcotics and / or drugs for neurocognitive purposes * Existence of a severe condition in general (cardiac, respiratory, hematological, renal, hepatic, cancerous) * Any other neurodegenerative pathology or treatment that may affect the oculomotor control For Parkinson patient: * Treatment for Parkinson's disease (except the inhibitors of monoaminoxidase B or MAO-B, such as selegiline and rasagiline).

Design outcomes

Primary

MeasureTime frameDescription
MRI images1 hourFunctional and anatomical brain volumes

Secondary

MeasureTime frameDescription
Eye latency1 hourlatency (milliseconds) of ocular saccades
eye amplitude1 houramplitude (degree) of ocular saccades

Countries

France

Contacts

Primary ContactCarole PEYRIN, PhD
carole.peyrin@gmail.com(0)4 7682-5879
Backup ContactLouise KAUFFMANN
louise.kauffmann@gmail.com

Outcome results

None listed

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