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
- Healthy
- Migraine
- Visual Snow Syndrome
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 60 Years
- Healthy Volunteers
- Accepted
Interventions
- Visual Adaptation — BEHAVIORALPresentation of visual stimuli to quantify the appearance of visual snow or its effects in the visual system of the brain.
- Assessments and Questionnaires — BEHAVIORALAdministration of clinical assessments and questionnaires to gather information about visual and mental symptoms, cognitive, and sensory function.
- Functional Magnetic Resonance Imaging (fMRI) — DEVICE7 tesla fMRI data will be acquired during visual paradigms designed to measure neural responses with and without adaptation.
- Magnetic Resonance Imaging (MRS) — DEVICE7 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
- Michael-Paul Schallmo, Ph.D.(612) 273-9130
- Hannah Moser, Ph.D.
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Minnesota | Minneapolis | Minnesota | 55455 |
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