Tinnitus Patient Preferences Survey
Nicolas Gninenko
500 participants
Jan 13, 2025
OBSERVATIONAL
Conditions
Summary
The goal of this survey is to assess several aspects related to patient preferences regarding interventions for alleviating tinnitus through invasive electrical brain stimulation (neuromodulation). This survey covers the acceptance of a surgically-placed brain implant, of its associated risks related to the neurosurgical procedure, usability considerations, and the willingness/ability to pay for such a treatment. Neurosoft Bioelectronics will use the collected patients' feedback and usability preferences data for the development of a novel minimally invasive brain implant aimed at alleviating tinnitus.
Eligibility
Inclusion Criteria2
- Individuals aged 18 or older suffering from subjective tinnitus
- Self-reported or healthcare professional-diagnosed chronic (lasting 3 months or longer), subjective, burdensome tinnitus
Exclusion Criteria2
- Individuals under 18 years of age
- Healthy volunteers without tinnitus
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Interventions
patients preferences survey
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06782308