Assessment of Customized Bimodal Stimulation for Tinnitus

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.

NCT Number	NCT07092033
Lead Sponsor	University of Minnesota
Conditions	Tinnitus
Enrollment	19 participants
Start Date	2025-07-31
Primary Completion	2025-12-29 (estimated)
Study Completion	2025-12-29 (estimated)
Updated on ClinicalTrials.gov	2026-08-04