Clinical Trial

Evaluation of a Non-invasive Tinnitus Device for the Management of Tinnitus Symptoms in Military Veterans

Completed
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Summary
The prevalence of tinnitus in military veterans is notably higher than the non-veteran population and can significantly disrupt the lives of veterans. Given the profound impact of tinnitus on the lives of veterans, along with the considerable economic burden and barriers to treatment, it is crucial to explore the feasibility of new approaches. Wearable sound technologies offer a non-invasive and easily accessible approach. As such, this waitlist-controlled trial aims to assess the efficacy of this new non-invasive white noise wearable device in reducing tinnitus symptoms between baseline and the one-month post-randomisation among veterans who have experienced tinnitus for at least three months.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-03-25; most recent amendment 2026-03-11.
Status change: Not Yet Recruiting → Completed 2026-03-11
Trial Details
NCT Number NCT06905158
Lead Sponsor Combat Stress
Conditions Tinnitus
Enrollment 20 participants
Start Date 2025-10-06
Primary Completion 2026-01-08 (estimated)
Study Completion 2026-01-08 (estimated)
Updated on ClinicalTrials.gov 2026-03-13