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Active, not recruitingNCT07913776Updated Nov 3, 2026

Performance of a Remote Microphone Compared to Hearing Aids Alone

An interventional study of Commercially available Receiver in the Canal (RIC) hearing devices and Hearing Aids plus Remote Microphone System in Hearing Loss, Bilateral Sensorineural, sponsored by Sonova AG. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years to 95 Years. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by Sonova AG · Not applicable, Interventional, and Treatment

Updated Nov 3, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years to 95 Years
Sex
All
01

Study summary

This study will compare speech understanding in noise using a remote microphone with hearing aids and compatible receivers with speech understanding in noise using hearing aids alone in a population of hearing impaired adults, age 18 and over. Participants will be tested in a near condition (target speech and remote microphone located 1 meter away from participant) as well as a far condition (target speech and remote microphone located 2 meters away from participant). Subjective questionnaire about listening effort and overall satisfaction will also be administered to each participant.

02

Conditions studied

  • Hearing Loss, Bilateral Sensorineural

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Keywords

  • hearing loss
03

In context

Hearing Loss

796 studies on the registry are indexed under Hearing Loss; 193 are open to participants now.

This study's planned enrollment of 20 is below the median of 44 across 561 interventional studies indexed under Hearing Loss.

Browse Hearing Loss studies →

Lead sponsor

Sonova AG is the lead sponsor of 89 studies on the registry; 6 are open to participants now.

Of its 27 completed or terminated interventional studies of FDA-regulated products, 19 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 95 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

18-95 years of age

  • Bilateral sensorineural hearing loss (e.g., N3, N4, S1)
  • Experienced hearing aid users (bilateral)
  • Fluent in English; ability to read and write in English
  • Able to produce a reliable study test result
  • Willing to comply with all study requirements

Exclusion criteria

Exclusion Criteria:

  • to medical device (MD) in this study: known or allergy to hearing instruments/domes
  • Limited/inconsistent/no prior use of hearing instruments
  • Limited mobility/not being able to come to scheduled appointments
  • Limited ability to describe listening impressions/experiences and the use of the hearing instruments/accessories • Known psychological disorders
  • Unilateral hearing loss
  • Single sided deafness
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    Treatment A first, then treatment B: Hearing aids plus remote microphone system first, then HA alone

    Participants who complete speech testing with the hearing aids plus the remote microphone system first, and then complete speech testing with HAs alone

    Device: Commercially available Receiver in the Canal (RIC) hearing devices · Device: Hearing Aids plus Remote Microphone System

  • Experimental
    Treatment B first, then Treatment A: HAs alone first, then HAs plus remote microphone system

    Participants who complete speech testing with hearing aids alone first, then complete speech testing with HAs plus remote microphone system

    Device: Commercially available Receiver in the Canal (RIC) hearing devices · Device: Hearing Aids plus Remote Microphone System

Interventions

  • DeviceCommercially available Receiver in the Canal (RIC) hearing devices

    Commercially available hearing aids that are the RIC form factor

  • DeviceHearing Aids plus Remote Microphone System

    Commercially available hearing aids in the RIC form factor plus the Remote Microphone system, which includes an embedded receiver in the hearing aids and a wireless remote microphone transmitter.

06

What researchers measure

Primary outcomes

  1. Speech Understanding in Noise Performance

    A validated test of speech understanding in which a sentence is presented from a loud-speaker 1-2 meters away from participant, while competing background noise is presented from four corner loud-speakers. The participant repeats as many words as they understand and a percentage correct is calculated for number correct out of total words presented. A higher score is better.

    Time frame: One day lab visit- participants will be tested during a 2 hour lab visit with no subsequent visits planned

Secondary outcomes

  1. Subjective Feedback

    Subjects will be asked for their feedback using a subjective questionnaire with questions on overall satisfaction of sound quality, listening effort, and noise intrusiveness. Questions will be presented as a scale to compare experience with and without the remote microphone system.

    Time frame: One day lab visit- participants will be tested during a 2 hour lab visit with no subsequent visits planned

07

Study locations

1 site
  • Phonak Audiology Research Center
    Aurora, Illinois 60504, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2026 (actual). Primary completion is estimated for Nov 2026, 1 month after the start.

Of 125 industry-sponsored interventional studies with no phase under Hearing Loss, half reached primary completion within 5 months of starting (the median), counting those still running; a quarter within 2 and three quarters within 15. This study's planned 1 month is below that.

Counting every sponsor, half of 321 studies reached it within 19 months; a quarter within 5 and three quarters within 42.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 27, 2026
First posted
Nov 3, 2026
StartActual
Oct 27, 2026
Primary completionEst.
Nov 30, 2026
CompletionEst.
Nov 30, 2026
Last update
Nov 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07913776
Lead sponsor
Sonova AG
Responsible party
Sponsor
First posted
Nov 3, 2026
Start date
Oct 27, 2026
Primary completion
Nov 30, 2026 (estimated)
Completion
Nov 30, 2026 (estimated)
Last update
Nov 3, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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