Visual Adaptation for Visual Snow
(VPVSS Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to understand the brain activity that causes Visual Snow Syndrome (VSS), a condition where people see static or snow-like dots in their vision. Researchers seek to determine if this syndrome links to specific brain pathways and pinpoint where this activity occurs in the brain. Participants will undergo visual tests and MRI scans to address these questions. The study will explore the concept of Visual Adaptation, which may play a role in VSS. Individuals with VSS who have had the condition for over three months and live near the study site in Minnesota might be suitable for the trial. As an unphased trial, this study offers a unique opportunity to contribute to groundbreaking research that could lead to a better understanding and treatment of VSS.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. However, it does exclude participants with current substance dependence or recent hallucinogenic substance use.
What prior data suggests that this method is safe for participants?
Research shows that visual adaptation might help people with Visual Snow Syndrome (VSS). Studies have found that getting used to visual noise can temporarily lessen the symptoms of visual snow for many people. In some cases, with extended adaptation, the symptoms even disappeared.
Sources report no specific side effects or negative reactions related to visual adaptation, suggesting that the treatment is likely easy to tolerate. The study focuses on understanding brain activity linked to VSS and uses non-invasive tests and MRI scans, making it safe for participants.
Overall, visual adaptation appears to be a safe option for managing visual snow symptoms. Always consult a healthcare provider before deciding to join any clinical trials.12345Why are researchers excited about this trial?
Researchers are excited about Visual Adaptation for Visual Snow Syndrome because it offers a new approach to managing this condition. Unlike traditional treatments like medications or lifestyle changes, which aim to manage symptoms, Visual Adaptation focuses on retraining the brain's visual processing. This method could potentially address the root cause of the syndrome rather than just alleviating symptoms. By targeting the way the brain interprets visual information, it holds promise for providing more lasting relief for individuals with Visual Snow.
What evidence suggests that visual adaptation could be effective for Visual Snow Syndrome?
This trial will compare the effects of visual adaptation on people with Visual Snow Syndrome (VSS) to a control group. Research has shown that adapting to visual patterns can reduce the severity of symptoms in people with VSS. In some studies, adapting to visual noise nearly eliminated visual snow for most participants over time. Specifically, one study found that 27 participants experienced a reduction of at least half in both the frequency and intensity of their visual snow symptoms. These findings suggest that visual adaptation could be a promising method for managing VSS symptoms, although further research is needed to fully understand its potential.12467
Who Is on the Research Team?
Michael-Paul Schallmo, Ph.D.
Principal Investigator
University of Minnesota, Department of Psychiatry and Behavioral Sciences
Stephen A Engel, Ph.D.
Principal Investigator
University of Minnesota, Department of Psychology
Michael S Lee, M.D.
Principal Investigator
University of Minnesota, Department of Ophthalmology and Visual Neurosciences
Abby Metzler, M.D.
Principal Investigator
University of Minnesota, Department of Neurology
Malgorzata Marjanska, Ph.D.
Principal Investigator
University of Minnesota, Department of Radiology
Carrie E Robertson, M.D.
Principal Investigator
Mayo Clinic, Rochester, Department of Neurology
Are You a Good Fit for This Trial?
This trial is for individuals with Visual Snow Syndrome (VSS), those experiencing postprandial fullness or migraines, and healthy volunteers. Participants should be able to undergo MRI scans and complete various assessments and questionnaires related to visual and mental symptoms.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Assessment
Participants undergo assessments and questionnaires to understand visual and mental symptoms, cognitive, and sensory function
Visual Judgement and MRI
Participants make visual judgements based on images and undergo MRI scanning
Follow-up
Participants are monitored for safety and effectiveness after assessments
What Are the Treatments Tested in This Trial?
Interventions
- Visual Adaptation
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Minnesota
Lead Sponsor
National Institutes of Health (NIH)
Collaborator
Mayo Clinic
Collaborator
National Eye Institute (NEI)
Collaborator