N/A
N=68
Clinical Validation of the Lexie Lumen Hearing Aid
Hearing Loss
Bottom Line
View on ClinicalTrials.gov: NCT05337748 ↗Enrolled (actual)
68
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: Abbreviated Profile of Hearing Aid Benefit (APHAB) — 30.1; 21.4 score on a scale (1-99)
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lexie Self Test and Fit Group (Device); Lexie Professional Test and Fit Group (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- hearX Group
- Primary completion
- Oct 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Abbreviated Profile of Hearing Aid Benefit (APHAB) |
30.1; 21.4 | — |
| SECONDARY International Outcome Inventory for Hearing Aids (IOI-HA) |
31; 31 | — |
| SECONDARY QuickSIN Speech in Noise Test |
1.6; 3.5 | — |
| SECONDARY Digits-in-noise Test (DIN) |
.50; 0.13 | — |
| SECONDARY Live Speech Mapping Using Real Ear Measurements (REM) |
0.6; 3.0; 1.3; 2.7; 4.7; 4.3 | — |
Summary
More than half a billion people globally have hearing loss. Most hearing loss is sensorineural, meaning that the hearing loss is irreversible and requires rehabilitation. The majority of people with hearing loss have mild to moderate degrees, for which the most effective treatment options are hearing aids. Over the past few years, there have been many developments in hearing technology and the service delivery models in which they are supplied. Traditional hearing care models include several visits to a qualified hearing professional who must both perform diagnostics and prescribe hearing aids, which in the past has been the only way to obtain hearing aids. However, newer developments include forms of self-fitting hearing aids that enable a user to perform threshold measurements to determine the degree of hearing loss and automatically program and fine-tune hearing aids. These devices are now becoming available as direct-to-consumer (DTC) or over-the-counter (OTC) hearing aids. Furthermore, alternative care models have been suggested to bolster access and uptake of assistive technology for hearing loss. Regulations on DTC and OTC hearing aids are starting to come into effect. In 2017, the FDA Reauthorization Act of 2016 directed the FDA to create a category for OTC hearing aids for adults with perceived mild-to-moderate hearing loss. In October 2021, the FDA formally proposed a rule to establish the OTC hearing aid category as part of this process. These changes in regulations would mean that soon, many of these self-fitting devices will become available. In response to these changes in service delivery models, the hearX group recently developed the Lexie Lumen hearing aids that can perform in-situ hearing threshold estimations and automatically prescribe hearing aid gain settings that closely approximate the gold-standard NAL-NL2 fitting prescription. This study aims to evaluate whether the performance of the novel Lexie self-test and self-fitting hearing aid is equivalent to the same hearing aid programmed professionally by an audiologist using a professionally obtained audiogram.
Eligibility Criteria
Inclusion Criteria
- Adults aged between the ages of 18 to 99 years, living in South Africa.
- Good English proficiency (measured using an online English proficiency test as well as self-report of English speaking competence)
- Must have a self-perceived hearing loss
- Mild to severe sensorineural hearing loss (thresholds <= 80 dB HL across frequencies bilaterally)
- Possession of a smartphone compatible with the Lexie app (iOS or Android)
- Access to mobile data to operate the Lexie app.
- Willingness and availability to participate in the study over a period of 45 days
Exclusion Criteria
- Normal hearing or profound hearing loss
- Active outer or middle ear disease
- Poor English proficiency
- Diagnosed cognitive impairment
Data sourced from ClinicalTrials.gov (NCT05337748). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.