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NCT Number: NCT06792110

Evaluation of Artificial Intelligence-Integrated Hearing Aids for Individuals with Hearing Loss

The goal of this clinical trial will be to evaluate the efficacy of artificial intelligence-integrated hearing aids in individuals with hearing loss. The main questions to answer are:

1. How effective is an artificial intelligence integrated hearing aid in improving speech perception in noise. 2. How does an artificial intelligence integrated hearing aid compare to currently available commercial hearing aids.

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Key information

About this study

Hearing loss is a leading cause of disability globally. Undertreated hearing loss has been associated with several deleterious sequelae, including social isolation, decreased quality of life, and cognitive decline. For a large portion of individuals with hearing loss, hearing aids remain the intervention of choice for improving communication, decreasing social isolation, and enhancing quality of life. Yet, less than 20% of hearing aid candidates choose to use them2. This is partly due to a perceived lack of benefit from hearing aids. Individuals who use hearing aids continue to report difficulty with speech perception in noisy environments with multiple speakers, such as parties, restaurants, and other complex auditory settings.

The investigators have developed a neural network that runs on-device to achieve real-time target speech hearing in realistic multi-talker environments. Using our neural network, the wearer can focus on speech from a target speaker by learning their unique speech cues while ignoring all interfering speech and noise in complex acoustic environments. The wearer is additionally able to use distance to separate sounds from the environment from target sounds to be amplified. Finally the wearer is also able to specificy categories of sound that will be amplified in environment.

This study will prospectively study a hearing aid implementing these algorithms on individuals with hearing loss. Participants will be randomized to utilizing one of two commercial hearing aids vs the experimental device. Participants will participate in listening tests in which they must identify the words spoken by a specific voice in multi-talker babble noise. The investigators will measure performance with the primary and secondary outcome measures listed elsewhere.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Minimum Age of 18 yo
  • Bilateral sensorineural hearing loss amenable to hearing aids
  • Able to give informed consent
  • Native English speaker
  • Able to wear a standard pair of hearing aids

Exclusion criteria

  • Unable to participate in informed consent
  • Use of a cochlear implant
  • Hearing loss not amenable to hearing aid use
  • Conductive hearing loss

Treatment and study plan

Artificial Intelligence Integrated Hearing Aid Use

Device

Participants in this arm will use the study-designed artificial intelligence-integrated hearing aid in the listening tasks. Participants will also perform the listening tasks without hearing aids to act as controls.

Phonak Infineo Hearing Aid

Device

Participants in this arm will use a fitted commercial hearing aid in the listening tasks. Participants will also perform the listening tasks without hearing aids to act as controls.

Oticon Real Hearing Aid

Device

Participants in this arm will use a fitted commercial hearing aid in the listening tasks. Participants will also perform the listening tasks without hearing aids to act as controls.

Primary outcomes

  1. Speech Reception Threshold

    Time frame: From enrollment in the study until completion of a one day listening test experiment.

    A measurement of difference in average speech reception threshold across all groups

  2. Awareness of Environmental Marker

    Time frame: From enrollment in the study until completion of a one day listening test experiment.

    During certain listening tasks, an environmental sound of concern (e.g. a siren, or alarm) will be played while the participant is tasked with identifying speech. Awareness of these sounds will be tested by reaction time to the sound and identification of the sound.

Secondary outcomes

  1. Preference Scores

    Time frame: From enrollment in the study until completion of a one day listening test experiment.

    Mean opinion scores about which device is preferred

  2. Sound quality

    Time frame: 5 minutes

    Mean opinion scores about subjective sound quality of respective devices

Study contacts

Contact information is provided by the study sponsor or research team.

Arun Raghavan, MD

CONTACT

[email protected]

206-616-2598

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 24, 2025
Registry last updated
Jan 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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