Skip to content

Efficacy of Amplification With Hearing Aids for Tinnitus Relief

Efficacy of Amplification With Hearing Aids for Tinnitus Relief: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03716544
Enrollment
64
Registered
2018-10-23
Start date
2018-11-01
Completion date
2023-12-31
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Impairment, Tinnitus, Subjective

Keywords

Tinnitus, Hearing Loss, Amplification, Sound Therapy

Brief summary

This study evaluates the treatment efficacy of tinnitus in people with mild hearing loss. One-third of participants will use hearing aid, one-third of participants will use customized music, while the other one-third participants will receive no treatment (waiting list control).

Detailed description

Acoustic stimulation could induce plastic changes in the auditory cortex, and tinnitus mechanisms have been viewed as a negative consequence of neural plasticity in the central nervous system after peripheral aggression. Cortical changes (neural activity in the deafferented cortical area was reduced but the adjacent frequencies of the hearing loss region activated more extensive cortical areas) occur after sensorineural hearing loss, while exposure to an acoustically enriched environment or using hearing aids may minimize or reverse the plastic tonotopic map changes in the auditory cortex. The use of hearing aids in tinnitus management for people with significant hearing loss will always be associated with an improvement in hearing handicap and quality of life, and that complicates the interpretation of how much hearing aids specifically affect tinnitus. Thus studies on tinnitus patients with mild hearing loss could be illuminating, and this population will be targeted in the present study.

Interventions

DEVICEAmplification with hearing aid

Use of hearing aids

DEVICECustomized music

Customized music delivered via an iPod

Sponsors

Chinese University of Hong Kong
CollaboratorOTHER
Education University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years old or above * can provide written informed consent * have a diagnosis of subjective tinnitus, i.e., the tinnitus can only be heard by the patient and there is no acoustic source * a tinnitus duration of more than one year * have pure-tone average between 20 and 40 dB HL * have bilateral symmetrical hearing loss (i.e. difference less than 15 dB) * have at least a medium level of distress caused by tinnitus as indicated with total scores above 30 on the TQ-CH * are committed to complete the 12-month follow-up

Exclusion criteria

* objective tinnitus, i.e. tinnitus produced by an internal acoustic source activating the cochlea and can be heard by another person * received other forms of tinnitus treatments within three months before the baseline assessment session * any history suggestive of psychiatric illness * psychological distress or depression as indicated with total scores at or above 15 on the Cantonese HADS * current hearing aid users * inability to complete the study as revealed by the medical reports

Design outcomes

Primary

MeasureTime frameDescription
The Tinnitus Functional Index (Chinese version) (TFI-CH)Change from baseline value at 3 months, 6 months and 12 months after the first day of treatment will be measured.TFI-CH is a 25-item self-administered questionnaire which assesses eight domains of tinnitus impact: intrusiveness; sense of control; cognitive; sleep; auditory; relaxation; quality of life (QoL); emotion. The total TFI score ranges 0 - 100, the higher score is indicative of greater problem with tinnitus.

Secondary

MeasureTime frameDescription
The Tinnitus Questionnaire (Chinese version) (TQ-CH) scoresChange from baseline value at 3 months, 6 months and 12 months after the first day of treatment will be measured.The TQ-CH is a 52-item questionnaire which assesses five dimensions of tinnitus complaint: emotional distress; auditory perceptual difficulties; intrusiveness; sleep disturbance; and somatic complaints. The total TQ score ranges 0 - 104, the higher score is indicative of greater problem with tinnitus.
The Tinnitus Handicap Inventory (Chinese version) (THI-CH) scoresChange from baseline value at 3 months, 6 months and 12 months after the first day of treatment will be measured.The THI-CH is a reliable 25-item self-administered Chinese QoL tool that quantifies the impact of tinnitus on daily living. The total THI score ranges 0 - 100, the higher score is indicative of greater tinnitus handicap.
Self-rated Visual Analogue Scale (VAS) on tinnitus loudnessChange from baseline value at 3 months, 6 months and 12 months after the first day of treatment will be measured.The subjects will be asked to rate the perceived loudness of their tinnitus on VAS, with inaudible (scale rating value = 0) and very loud (scale rating value = 100) as reference points for the ends of the scale. The higher rating is indicative of louder tinnitus.
Tinnitus loudness matches at the tinnitus frequency and at 1000 HzChange from baseline values at 3 months, 6 months and 12 months after the first day of treatment will be measured.Tinnitus loudness matches will be done according to Vernon and Meikle's procedure
The Chinese Hospital Anxiety and Depression Scale (HADS)Change from baseline value at 3 months, 6 months and 12 months after the first day of treatment will be measured.The Chinese HADS is a 14-item questionnaire that consists of two subscales that measure anxiety and depression. It serves as an outcome measure targeting psychological and mental health effects.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026