Study of Visual Perception Phenomena: Phosphene Mapping Induced by TMS and Its Relationship With Eye Movements

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this basic science study is to better understand human visual perception. Phosphenes are flashes of light that can be induced using Transcranial Magnetic Stimulation (TMS). The location of these phosphenes is known to change with eye movements, but the exact influence of these movements is not fully understood. The main questions this study aims to answer are: How does stimulating specific areas of the visual cortex relate to where a person perceives a phosphene? How do eye movements affect the accuracy of mapping these sensations? The study will enroll three groups of adults (aged 18-65): patients with Visual Snow Syndrome, color-blind participants, and healthy volunteers. During the experiment, participants will receive single-pulse TMS to their visual cortex. Simultaneously, their eye movements will be monitored with an eye-tracker, and their brain activity will be recorded with EEG. Participants will be asked to report the location of the perceived light flashes. This will help create a map of the brain areas responsible for visual sensations and clarify how eye movements influence this process.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: t
View:

• For the Patients with Visual Snow Syndrome Arm:

• Confirmed diagnosis of Visual Snow Syndrome according to the International Classification of Headache Disorders, 3rd edition (ICHD-3) criteria.

• Presence of persistent, dynamic, tiny dots (visual snow) across the entire visual field.

• Presence of at least one of the following additional visual symptoms:

• Palinopsia (prolonged afterimages). Photophobia (hypersensitivity to light). Nyctalopia (impaired night vision). Blurred vision. Patients whose symptoms appeared after a SARS-CoV-2 viral illness may be included.

• For the Color-blind Participants Arm:

• Presence of a color perception disorder. Must have a formal diagnosis of color blindness confirmed by specific ophthalmologic tests (e.g., Ishihara, Rabkin, Justova, or Stilling polychromatic plates, or the Farnsworth-Munsell test).

• For the Healthy Controls Arm:

• Absence of any active or past neurological, psychiatric, or ophthalmological disorders.

Locations
Other Locations
Russian Federation
Skolkovo Institute of Science and Technology (Skoltech)
RECRUITING
Moscow
Contact Information
Primary
Akinshin R.
Roman.Akinshin@skoltech.ru
79999810206
Time Frame
Start Date: 2025-09-10
Estimated Completion Date: 2026-12-10
Participants
Target number of participants: 50
Treatments
Experimental: Patients with Visual Snow Syndrome
Participants diagnosed with Visual Snow Syndrome according to ICHD-3 criteria. This group will undergo TMS, EEG, and eye-tracking to study the mechanisms of visual perception.
Experimental: Color-blind Participants
Participants with a confirmed diagnosis of color blindness. This group will undergo TMS, EEG, and eye-tracking to compare visual processing with other groups.
Active_comparator: Healthy controls
Healthy volunteers with no history of neurological, psychiatric, or visual disorders. This group serves as a baseline to compare the findings from the experimental arms.
Related Therapeutic Areas
Sponsors
Collaborators: I.M. Sechenov First Moscow State Medical University
Leads: Skolkovo Institute of Science and Technology

This content was sourced from clinicaltrials.gov