MedPath

Hearing aids and tinnitus

Phase 3
Completed
Conditions
<p>Tinnitus</p>
10019243
Registration Number
NL-OMON28370
Lead Sponsor
niversity Medical Center Groningen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
18
Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all of the following criteria: - No reported neurological or psychiatric disorders (excluding tinnitus and hearing loss); - High frequency hearing loss; - Moderate- to moderate-severe- degree of hearing loss (PTA of 1, 2 and 4 kHz = 35 dB); - Chronic tinnitus (lasting more than 6 months); - Tinnitus percept described as tonal (or at least being able to perceive a pitch during a tinnitus matching); - Tinnitus pitch = 6 kHz, and in the hearing loss region; - Using hearing aids for at least the last 6 months; - Written informed consent;

Exclusion Criteria

Non-conformance to any of the inclusion criteria stated above;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br><tr><br><td>There was a small reduction of the TFI score after the adaptation process, possibly due to a placebo effect.&nbsp; The TFI score&nbsp; did not differ significantly from the standard setting after using the notched or the boosted settings. Regardless of the TFI outcomes, most participants had an individual preference for a particular setting. Notch-filtered and boosted amplification did not provide better tinnitus suppression than standard amplification, although notched amplification performed better than boosted amplification. The individual preferences highlighted the importance of tailor-made approaches to hearing aid amplification in clinical practice. Further studies should explore the differences among patient’s tinnitus and their preference for a hearing aid setting.&nbsp;</td><br></tr><br><br>
Secondary Outcome Measures
NameTimeMethod
<p>Additionally, the following psychoacoustic measures will take place: - Changes in tinnitus pitch - Changes in tinnitus loudness - Auditory Handicap - Hours of hearing aid use</p><br>
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