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Evaluation of Investigational Hearing Instrument Features

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Sonova

Status

Not yet enrolling

Conditions

Hearing Loss

Treatments

Device: Hearing instrument

Study type

Interventional

Funder types

Industry

Identifiers

NCT06710236
SRF-26463

Details and patient eligibility

About

The goal of this clinical trial is to learn how hearing instruments perform in varying environmental settings in adults with hearing loss. The main questions it aims to answer are:

How do varying versions of hearing instrument features perform based on exposure to different environments? What is the hearing instrument user preference between varying versions of hearing instrument features?

Participants will be fit with hearing instruments in the lab, and asked to wear them for the duration of the study period in their home environment. Participants will be asked to answer questionnaires throughout the study period.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult, age 18 - 95 years
  • N4 hearing loss
  • Experienced hearing aid user
  • English fluency
  • Cognitively able to complete complex listening tasks

Exclusion criteria

  • Normal hearing, or hearing loss outside the specified range
  • No hearing aid experience
  • Unable to speak, read, or write English fluently
  • Cognitive impairment
  • Any other condition or situation that impacts eligibility to participate in or complete study tasks, at the discretion of the investigator

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Hearing Aid Users
Experimental group
Description:
Participants will wear hearing instruments for the duration of the study period. They will be asked to complete questionnaires about their environment and experience.
Treatment:
Device: Hearing instrument

Trial contacts and locations

1

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Central trial contact

Research Audiologist

Data sourced from clinicaltrials.gov

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