Real World Perspectives on Advancements in Hearing Aid Technology

NCT ID: NCT05468918

Last Updated: 2023-08-22

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

14 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-18

Study Completion Date

2022-10-26

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will compare different microphone technologies in a noisy environment when the dominant speaker is at the front, back, left, or right side of the listener.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Understanding speech in a noisy environment can be difficult for people with hearing loss even with hearing aids. Hearing aid manufacturers have implanted various methods (i.e., directional micro-phones, noise reduction, noise cancelers) to try to improve the signal-to-noise ratio (SNR) to increase the speech understanding in these difficult listening situations.

This study is evaluating different microphone technologies to determine listening effort when speech is to the back or side of the listener in noisy environment.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hearing Loss

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
Participants were blinded as to which device they were wearing during the lab testing.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Participants tested with comparator devices first, then Audeo Lumity devices

All participants who completed speech in noise testing in the lab with the comparator devices first, and then the Audeo Lumity devices.

Group Type EXPERIMENTAL

Phonak Audeo previous generation hearing aids

Intervention Type DEVICE

Receiver-in-canal (RIC) hearing aids with universal earpieces

Phonak Audeo Lumity hearing aids

Intervention Type DEVICE

Receiver-in-canal (RIC) hearing aids with universal earpieces

Participants who were tested with Audeo Lumity first, then comparator devices

All participants who completed speech in noise testing in the lab with the Audeo Lumity devices first, and then the comparator devices.

Group Type EXPERIMENTAL

Phonak Audeo previous generation hearing aids

Intervention Type DEVICE

Receiver-in-canal (RIC) hearing aids with universal earpieces

Phonak Audeo Lumity hearing aids

Intervention Type DEVICE

Receiver-in-canal (RIC) hearing aids with universal earpieces

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Phonak Audeo previous generation hearing aids

Receiver-in-canal (RIC) hearing aids with universal earpieces

Intervention Type DEVICE

Phonak Audeo Lumity hearing aids

Receiver-in-canal (RIC) hearing aids with universal earpieces

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Moderate sensorineural hearing loss
* Experienced hearing aid user
* Has a significant other/communication partner that can fill out a questionnaire about hearing aid performance during the home trial
* Smartphone user for receiving study alerts

Exclusion Criteria

* Cognitive impairment
* Not willing to wear hearing aid
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Sonova AG

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Phonak Audiology Research Center

Aurora, Illinois, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

SRF-2855

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.