Feasibility and Acceptability of Using Low-Gain Hearing Aids for Bothersome Tinnitus
Project Number1I21RX003196-01
Contact PI/Project LeaderZAUGG, TARA LYNETTE
Awardee OrganizationPORTLAND VA MEDICAL CENTER
Description
Abstract Text
Tinnitus – defined as ringing, humming, or other sounds in the ears or head – is the most prevalent service-
connected disability among Veterans. Tinnitus affects 10-15% of the adult population. For about 20% of these,
tinnitus impacts their lives with respect to sleep disturbance, impaired concentration, and/or emotional
reactions. These 20% are the most in need of clinical services. It has been shown that providing amplification
via hearing aids for people with hearing loss can also be beneficial in reducing functional effects of tinnitus,
presumably because amplifying environmental sounds reduces the contrast between the tinnitus and
background sound, allowing the tinnitus to be more easily ignored. There have been increasing reports from
the field of audiologists providing hearing aids set to deliver low-gain amplification on patients with bothersome
tinnitus who are not otherwise hearing aid candidates, with beneficial outcomes. However, this nontraditional
fitting practice has not been formally evaluated, so there is no research evidence to support the practice. It is
essential for VA to show evidence supporting such practices to justify the use (and expense) of these devices
with patients who otherwise do not qualify to receive hearing aids.
The proposed project is a pilot study that would lay the groundwork for a future full randomized controlled trial
(RCT) evaluating the use of low-gain amplification for bothersome tinnitus in patients with normal hearing. A
pilot sample of 20 Veterans with normal hearing thresholds and bothersome tinnitus will be fit with mild
amplification through receiver-in-the-canal hearing aids. Hearing aids will be programmed to provide a low-
level of amplification, using NAL-NL2 guidelines for target gain. Outcome measures will be evaluated pre-fit
and post-fit at two follow-up time points (2 weeks and 3 months post-fit). Outcomes will include the Tinnitus
Functional Index (TFI), Hearing Handicap Inventory for Adults (HHIA) and the Quick Speech in Noise
(QuickSIN) test. Outcomes pre and post hearing aid fit will be compared to evaluate whether the hearing aids
provided benefit to participants in terms of their tinnitus and hearing outcomes. Additionally, participants will be
interviewed at their last visit to find out their self-reported benefit from the hearing aids, as well as any barriers
they encountered to wearing the hearing aids.
Additionally, a group of VA clinical audiologists will be interviewed by telephone. These clinicians will be
identified via an email survey sent to the VA audiologist email group, asking whether they are providing low-
gain amplification for bothersome tinnitus to patients with normal hearing. The survey will also ask audiologists
to volunteer if they are willing to participate in a brief telephone interview. The aim will be to identify at least ten
audiologists who are fitting hearing aids in this way, and up to five who are not. These audiologists will be
interviewed over the telephone to find out why they have incorporated this into their clinical practice (or why
they have not), and inquire about specific fitting procedures and criteria for identifying candidates that they
have used. These responses will inform the protocol of the future RCT.
At the conclusion of this project, enough information will be collected to propose a controlled study of low-gain
amplification for bothersome tinnitus in people with normal hearing. The protocol for that project will be
informed by both the successful aspects of the pilot protocol as well as the input from VA clinicians who are
doing this in the field. A preliminary evaluation of benefit provided by these hearing aids will provide justification
for a large controlled study. Finally, the pilot data will provide the basis for a power calculation to determine
sample size, as well as an estimate of drop-out rate to sufficiently adjust for attrition. A full RCT demonstrating
efficacy of low-gain amplification for bothersome tinnitus in people with normal hearing would provide needed
evidence supporting a clinical practice that has already gained some traction both within and outside VA.
Robust research evidence is needed to support the continuation and future expansion of this practice.
Public Health Relevance Statement
Tinnitus – defined as ringing, humming, or other sounds in the ears or head – is a very common problem for
Veterans. Hearing aids that deliver low-level amplification are being used by audiologists to help people with
tinnitus who also have normal hearing. However, there is a lack of research evidence showing that this practice
is effective. Despite this fact, the practice clearly is spreading. Reports from audiologists in the field as well as
research presentations refer to hearing aids being used in this way. Use of hearing aids has been shown to
reduce distress from tinnitus for people with hearing loss. Additionally, the use of external sound to help reduce
the impact of tinnitus has been shown to be effective. There is clearly a gap in the research regarding the use
of hearing aids as a therapeutic method to manage tinnitus when hearing is considered normal. This study will
obtain pilot data evaluating Veterans with normal hearing and bothersome tinnitus to find out whether low-level
amplification through hearing aids may provide benefit.
No Sub Projects information available for 1I21RX003196-01
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 1I21RX003196-01
Patents
No Patents information available for 1I21RX003196-01
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 1I21RX003196-01
Clinical Studies
No Clinical Studies information available for 1I21RX003196-01
News and More
Related News Releases
No news release information available for 1I21RX003196-01
History
No Historical information available for 1I21RX003196-01
Similar Projects
No Similar Projects information available for 1I21RX003196-01