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MRI Study of Saccadic Adaptation

Coupling Between Saccadic Adaptation and Visuospatial Perception Process: MRI Study in Humans

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03488082
Enrollment
36
Registered
2018-04-04
Start date
2018-10-17
Completion date
2020-07-17
Last updated
2025-09-03

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

Conditions

Healthy Volunteers

Keywords

saccadic adaptation, visual-spatial perception, fMRI

Brief summary

Accurate execution of our directed behaviors in the immediate environment allows the vast majority of our daily activities. Through the movements of our eyes and different parts of our body, we perceive, explore and act on our environment and can exchange and communicate with others. The mechanisms of sensorimotor adaptation of saccades (saccadic adaptation) contribute on the one hand to maintain the accuracy of saccades in the short, medium and long term, by opposing the deleterious effects of various physiological changes (development, aging), pathological or environmental (optical corrections). The aim of this study is to identify neuronal structures and networks involved in saccadic adaptation through the study of brain metabolic activation (BOLD) during the development of the adaptation of reactive saccades. The study will be organized in a single session with 3 runs. Each run include 4 blocks: 3 include the double-step target paradigm RND, U+, U-) and one without target jump (STA). The 'U+'/ 'U-'blocks include saccadic trials with forward/backward displacement of the target during a targeting saccade, the 'RND' block include saccadic trials with random target jump (forward or backward) and the 'STA' block are trials without displacement of the target. Each subject will make 12 repetitions of the 4 blocks.

Interventions

BEHAVIORALfMRI

saccadic adaptation (target presentations, with or without target jump) during fMRI exam

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

\- Age: 18 to 40 years included,

Exclusion criteria

* Known ophthalmological or neurological pathology, * Non-stabilized medical condition, * Taking psychotropic treatment, * No fluency in reading in French, * Pregnant and / or breastfeeding woman

Design outcomes

Primary

MeasureTime frameDescription
BOLD signalthroughout the behavioral experiment at Day 1cerebral activations with fMRI measures when the subject fixates or shifts gaze toward visual targets (behavioral tasks).

Secondary

MeasureTime frameDescription
Eye movementsduring the development of saccadic adaptation (throughout the behavioral experiments at Day 1)measurement of the eye movements (saccades) of the subject while fixating and shifting gaze toward visual targets (behavioral tasks).

Countries

France

Outcome results

None listed

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