Skip to main content
Clinical Trials/ACTRN12621001754831
ACTRN12621001754831
Completed
N/A

A 3 month trial of the Oticon Tinnitus Sound Support feature in hearing aids for adults with hearing loss and tinnitus using the Tinnitus Functional Index as the primary outcome measure.

The University of Auckland0 sites40 target enrollmentDecember 22, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Tinnitus
Sponsor
The University of Auckland
Enrollment
40
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Results confirm previous findings that hearing aids assist in reducing the impact of tinnitus on daily life. The Oticon miniRITE combination hearing aids used in this study resulted in similar improvements for new and existing hearing aid users. This suggests tinnitus-reducing effects of these aids was greater than those already being used by participants.

Registry
who.int
Start Date
December 22, 2021
End Date
December 12, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria were: Adults aged 18 years or above; Chronic tinnitus (at least 6 months since onset); New and experienced HA users with a symmetric slight (16 dB HL) to moderately severe (70 dB HL) binaural symmetric (PTA4 difference between ears of 15 dB or less) sensorineural or mixed flat or sloping hearing loss; HA fitting level for the 60\- or 85\-dB speaker and domes, or custom moulds including all types and configurations of hearing loss; Scores in the range of ‘Normal to Severe’ in each of the three categories on the Depression Anxiety and Stress Scale – 21 Items (DASS 21\).

Exclusion Criteria

  • Absence of tinnitus or hearing loss. A score of ‘Extremely Severe’ in any one of the three categories of the DASS 21; Objective, pulsatile tinnitus.

Outcomes

Primary Outcomes

Not specified

Similar Trials