Skip to main content
OpenTrials
Completed

NCT Number: NCT05666505

Evaluation of a New mHealth Tympanometer

Children in rural and underserved communities experience a disproportionately high burden of infection-related hearing loss, which is often preventable with timely identification and follow-up care. A tympanometer is a device that evaluates the health of the middle ear but is often not used in screening programs due to barriers of high cost and need for trained professionals such as audiologists to use the device. To address these barriers, a low cost, lay friendly, mobile health (mHealth) prototype tympanometer has been developed. In addition, a machine learning (ML) algorithm has been designed to guide lay users to interpret tympanometer results, overcoming the need for audiologists. Broad implementation of the lay friendly tympanometer and ML algorithm will transform screening in areas where prevalence of infection-related hearing loss is high, and access to specialty care is limited.

In this study the prototype mHealth tympanometer will be evaluated against commercial tympanometry. It will be used by audiologists, an essential step before testing the performance of the device with lay users. Approximately 20 adult patients and 10 pediatric patients with various middle ear pathologies will be enrolled in the study, with the goal of obtaining 60 ears with data from both the prototype and commercial tympanometers. Audiologists will obtain tympanometry measurements on both ears of each participant and interpret the results, first with the prototype device and then with the commercial tympanometer that is typically used during a clinical evaluation. Tympanometry interpretation will include classification into one of 3 categories (Type A, B, or C). Agreement in results between the prototype and commercial devices will be assessed. Agreement between audiologist interpretations and the ML algorithm from the prototype mHealth tympanometer will be assessed.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Presenting to Audiology Clinic for evaluation, where tympanometry is warranted for testing at the discretion of the audiologist
  • Presence of various middle ear health states/pathologies that result in Type A, B, C tympanograms
  • English-speaking

Exclusion criteria

  • Children or adults with cognitive disabilities
  • Unable to provide consent/assent
  • Individuals who are unable to sit still
  • Any other condition that in the opinion of the investigator, might interfere with the safe conduct of the study or place the participant at increased risk

Treatment and study plan

Prototype mHealth tympanometer

Device

The prototype mHealth tympanometer functions similarly to a commercial tympanometer. Tympanometers are designed to assess middle ear function by measuring changes in acoustic tone related to subtle movement of the tympanic membrane from an applied air pressure sweep. An audiologist will review the tympanogram tracings and classify results as Type A, B, or C.

Standard of care commercial tympanometer

Device

A commercial tympanometer routinely used as part of standard of care will be used as the comparison. Tympanometers are designed to assess middle ear function by measuring changes in acoustic tone related to subtle movement of the tympanic membrane from an applied air pressure sweep. An audiologist will review the tympanogram tracings and classify results as Type A, B, or C.

Primary outcomes

  1. Classification Agreement Between Prototype mHealth Tympanometer and Commercial Tympanometer

    Time frame: Same day as participant visit, up to 10 minutes

    Audiologist will test each ear of the participant first with the prototype device, interpret the results into one of the three tympanogram categories (Type A/B/C) and record the results. The procedure will be repeated with a commercial device. Agreement between the two devices with respect to the classification categories will be assessed.

  2. Classification Agreement Between Audiologist and ML Algorithm Interpretations Using Prototype mHealth Tympanometer

    Time frame: Same day as participant visit, up to 10 minutes

    Tympanogram results collected using the prototype mHealth tympanometer will be run through the ML algorithm for classification into Type A/B/C. Agreement between the audiologist and the ML algorithm with respect to the classification categories will be assessed.

Sponsors and collaborators

Lead sponsor

University of Arkansas

Other

Registry information

Official study title

A Pilot Study to Assess Performance of a New Low-Cost Mobile Health Based Prototype Tympanometer

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Dec 27, 2022
Registry last updated
Jan 13, 2026

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.

Published trials that share one or more normalized conditions with this study.