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The research objective of the proposed usability study is to assess the compliance and acceptance/satisfaction of using a bimodal stimulation device with the modification of the sound stimulus to the participant's tinnitus pitch. In particular, the sound stimulus will not contain the pitch of the tinnitus, which may increase comfort and usability with the device since it will be customized to their tinnitus. Furthermore, virtual follow-up assessments and/or phone calls will be performed, thus significantly reducing the burden and personnel requirements for in-person visits as originally performed with the current clinic process.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Minnesota - PWB
Minneapolis, Minnesota, United States
Start Date
July 31, 2025
Primary Completion Date
July 1, 2026
Completion Date
July 1, 2026
Last Updated
October 9, 2025
20
ESTIMATED participants
Bimodal Neuromodulation
DEVICE
Lead Sponsor
University of Minnesota
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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View ClinicalTrials.gov Terms and ConditionsNCT06641999