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Hearing Aid Transmitter Performance Study - SRF-366

Hearing Aid Transmitter Performance Study - SRF-366

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04774185
Enrollment
23
Registered
2021-03-01
Start date
2021-04-26
Completion date
2022-04-25
Last updated
2023-03-28

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

Conditions

Hearing Loss

Keywords

Acoustical Coupling

Brief summary

Sonova Hearing Systems pass through different development and study stages. At an early stage, feasibility studies are conducted to investigate new algorithms, features and functions in an isolated manner. If the benefit is proven, their performance is then investigated regarding interdependency between all available algorithms, features and functions running in parallel in a hearing aid (pivotal/pre-validation studies) and, as a result, they get optimized. Afterwards, and prior to product launch, the Sonova Hearing Systems undergo a final quality control in terms of clinical trials. This is a confirmatory study, investigating benefits of a modified hearing aid loudspeaker. This will be a clinical investigation which will be conducted mono centric at National Acoustic Laboratories a well known institution with exceptional experience (Australia).

Detailed description

In this study a comparison with two Phonak Receiver in Canal (RIC) devices is done. The experimental device with a modified hearing aid loudspeaker concept and the active comparator with the existing technology will be compared regarding speech intelligibility, listening effort and sound quality in speech in noise, quiet situations for people with mild to moderate hearing losses.

Interventions

DEVICENew hearing aid loudspeaker

The new hearing aid loudspeaker will be fitted to the participants individual ear anatomy and hearing loss.

DEVICEStandard hearing aid loudspeaker

The standard hearing aid loudspeaker will be fitted to the participants individual ear anatomy and hearing loss.

Sponsors

Sonova AG
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Adult hearing impaired persons (minimum age: 18 years, mild to moderate Hearing loss) * Good written and spoken English language skills * Healthy outer ear * Ability to fill in a questionnaire (p/eCRF) conscientiously * Willingness to wear Receiver in Canal hearing aids * Informed Consent as documented by signature * Normal cognitive abilities

Exclusion criteria

* Contraindications to the MD in this study, e.g. known hypersensitivity or allergy to the investigational product * Limited mobility and not in the position to attend weekly appointments in Sydney (AUS) * Limited ability to describe listening impressions/experiences and the use of the hearing aid * Inability to produce a reliable hearing test result * Known psychological problems

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of speech intelligibility and sound quality for different loudspeaker2 weeksThe Primary Outcome measure of this study is the comparison of the standard hearing aid loudspeaker with the modified one in regard to speech intelligibility in a noisy environment and sound quality in a quiet situation. The speech intelligibility will be measured using a speech test in dB SRT and the sound quality will be assessed by subjective rating, using percentage of satisfaction from very satisfied (100) to very unsatisfied (0).

Secondary

MeasureTime frameDescription
Evaluation of listening effort for different loudspeaker.2 weeksThe Secondary Outcome measure of this study is the comparison of the standard hearing aid loudspeaker with the modified one in regard to listening effort in a noisy environment. The listening effort of speech will be assessed by subjective rating, within 13 steps, from not effortful at all to only noise.
Evaluation of sound quality of own voice for different loudspeaker.2 weeksThe Secondary Outcome measure of this study is the comparison of the standard hearing aid loudspeaker with the modified one in regard to sound quality in quiet. The sound quality of own voice will be assessed by subjective rating, using percentage of satisfaction from very satisfied (100) to very unsatisfied (0).
Evaluation of sound quality of streamed signals for different loudspeaker2 weeksThe Secondary Outcome measure of this study is the comparison of the standard hearing aid loudspeaker with the modified one in regard to sound quality of a streamed signal in quiet and noise.. The sound quality of the streamed signal will be assessed by subjective rating, using percentage of satisfaction from very satisfied (100) to very unsatisfied (0).

Countries

Australia

Outcome results

None listed

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