Clinical Trials Directory

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UnknownNCT04902365

Neurofeedback in Visual Snow

Neurofeedback for Patients With Visual Snow

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
University of Zurich · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

Visual snow (VS) is a distressing, life-impacting condition with unrelenting and persistent disturbing visual phenomena. Disease onset is usually around age 20 and is characterized by continuous perception of innumerable flickering dots (like a 'broken television'). The disease is often accompanied by comorbidities such as migraine, tinnitus, depression and anxiety. Neuronally, VS patients show cerebral hypermetabolism, resulting in altered neuronal excitability, as well as increased grey matter volume in parts of the visual cortex. For this pilot study, the investigators aim to recruit VS patients. In a double-blind, randomized and placebo-controlled longitudinal experiment, the investigators will use real-time functional magnetic resonance imaging (rtfMRI) neurofeedback to teach patients to downregulate activity in different regions of the visual cortex. The investigators hypothesize that neurofeedback will allow patients to learn to downregulate their abnormal visual cortex activity. Moreover, the investigators predict that a stronger downregulation of activity from the lingual gyrus will correlate with a more pronounced decrease in VS symptoms.

Detailed description

Currently, there is no pharmacological or non-pharmacological treatment available that significantly reduces the high disease burden produced by VS. Thus, there is an unmet need for an appropriate intervention to treat patients with VS. In this study, the investigators will: 1. Test if rtfMRI-based neurofeedback could serve as therapeutic option for patients with VS. Here, the investigators will examine correlations of neurofeedback regulation success with clinical scores 3 after neurofeedback 2. Examine brain function and structure in patients with VS Primary and secondary endpoint/outcome(s) * Primary outcome variable: VS symptom severity before and after rtfMRI, using standardized clinical assessment. * Secondary outcome variables: fMRI and structural MRI, clinical questionnaires (visual function, anxiety, depression, tinnitus, and migraine), parameters from psychophysical data (assessed before and after neurofeedback). * Linear Mixed model analysis will be performed (using clinical and imaging data) to estimate the impact of rtfMRI on clinical progression and brain function/structure.

Conditions

Interventions

TypeNameDescription
OTHERneurofeedback(based on real-time functional magnetic resonance signals)

Timeline

Start date
2022-01-14
Primary completion
2023-08-30
Completion
2023-12-30
First posted
2021-05-26
Last updated
2023-06-15

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT04902365. Inclusion in this directory is not an endorsement.