Investigating Brain Function in People With and Without Visual Snow Syndrome Using Adaptation to Visual Stimuli

Part of paid clinical trials in Minneapolis, Minnesota.

Sponsor
University of Minnesota
Study ID
NCT06961864
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 60 Years
Healthy Volunteers
Accepted

Interventions

  • Visual Adaptation — BEHAVIORAL
    Presentation of visual stimuli to quantify the appearance of visual snow or its effects in the visual system of the brain.
  • Assessments and Questionnaires — BEHAVIORAL
    Administration of clinical assessments and questionnaires to gather information about visual and mental symptoms, cognitive, and sensory function.
  • Functional Magnetic Resonance Imaging (fMRI) — DEVICE
    7 tesla fMRI data will be acquired during visual paradigms designed to measure neural responses with and without adaptation.
  • Magnetic Resonance Imaging (MRS) — DEVICE
    7 tesla MRS data will be acquired to quantify the concentrations of different brain chemicals in brain regions including visual cortex.

Study Details

The goal of this study is to learn more about the brain pathways and activity involved in creating Visual Snow Syndrome (VSS). The main questions it aims to answer are: * Does VSS arise from spontaneous activity in brain pathways? * Where in the brain does the activity contributing to VSS arise? * How does brain activity contribute to VSS? Participants will: 1. Undergo assessments and questionnaires to understand visual and mental symptoms, cognitive, and sensory function. 2. Make visual judgements based on images presented to them both inside and outside a magnetic resonance imaging (MRI) machine. 3. Undergo scanning of their brain while inside of an MRI machine.

Key Dates

Start date
Apr 11, 2025
Status verified
Jan 2026
Primary completion
Mar 31, 2030
Completion
Mar 31, 2030

Study Design

Enrollment
100 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE

Arms

  • Active Comparator: People with Visual Snow Syndrome
  • Placebo Comparator: Non-snow Controls

Primary Outcome Measure

Psychophysical Adaptation Task Performance [ Time Frame: 1.5-2 hours per session, with experiments divided across multiple (e.g., 3) sessions ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of MinnesotaMinneapolisMinnesota55455
Michael-Paul Schallmo, Ph.D., Assistant Professor
612-273-9130

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