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Status unknownNCT02761798Updated Apr 10, 2018

The Automated Mobile Interactive Audiometer - Feasibility and Reliability in a Clinical Setting

An observational study in Hearing Loss, sponsored by Matt Bromwich. Status unknown at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-04-10.

Sponsored by Matt Bromwich · Observational

The sponsor has not verified this record recently (last verified Apr 2018), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
120
Ages
18 Years and older
Sex
All
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Study summary

This observational study aims to validate the use of a tablet based audiometer to provide an accurate, efficient, and cost-effective means for diagnosis of hearing conditions in controlled and uncontrolled environments in adult and elderly populations.

Read the detailed description

In the 2011 report on Disability, the World Health Organization rated hearing loss as the most prevalent disability in the world. More than 30% of adults have disabling hearing loss complicating the management of their comorbid diseases. Isolation, mental illness and lack of family support are just some of the negative impacts of this invisible disability. In the next 25 years the number of hearing impaired individuals over the age of 65 in Canada will double, while at the same time there is a projected 50% shortfall in audiological service providers. The resultant service deficit is compounded by the lack of equipment and familiarity with hearing healthcare at the primary care level, causing increased inefficiency, unnecessary referrals, and unmet needs.

In Canada, there is a critical need to improve the number of health professionals with the requisite skills to meet the needs of the aging population. This project is aimed at developing a novel approach to address the increasing need for hearing healthcare in the adults while managing the strain on the healthcare system.

Healthcare workers (such as general practitioners, registered nurses and allied heath workers) can play an important role in supporting and motivating adults to seek help and aid in the referral process. However, few healthcare workers receive formal training in the identification, diagnosis, treatment options, referral process, and special needs of older adults with hearing loss. This lack of training, resources and equipment is a significant gap in the care provided to the elderly and impacts all other aspects of elder care.

Undiagnosed/untreated hearing loss can lead to physiological changes associated with auditory deprivation, as well as psychosocial changes of social isolation and depression. It can result in emotional, physical, cognitive, and behavioral consequences including impaired activities of daily living, decline in independence and reduced quality of life. In spite of the prevalence and impact of hearing loss and the benefits of rehabilitation in reducing the psychological, social, and emotional consequences of hearing loss, referral by physicians for assessment and rehabilitation is low and the majority of adults who could benefit from the use of hearing aids do not use this technology. Early identification can help to reduce these deleterious effects, and lead to easier adjustment to hearing aid use.

In spite of the numerous recent technological advances in field of hearing amplification devices, current technologies may not be effective for older adults who have central auditory processing and cognitive processing difficulties. Additionally, untreated hearing loss lowers performance on aurally administered diagnostic tests used to quantify the severity of dementia and can significantly confound the clinical picture in this population. Furthermore, the use of amplification is associated with reduction in problem behavior in persons with a primary diagnosis of Alzheimer's disease and a reduction in hearing handicap for persons with Alzheimer's disease and their significant others.

This study aims to validate the use of a tablet based audiometer to provide an accurate, efficient, and cost-effective means for diagnosis of hearing conditions in controlled and uncontrolled environments in adult and elderly populations.

Observations between the soundbooth and iPad audiograms will include the following frequencies 250, 500, 1000, 2000, 4000, 6000 and 8000 Hz. Each iPad audiogram consists of an interactive game that takes approximately 10-20 minutes to complete. The conventional audiogram will take place before the iPad audiogram. We expect our study to add a maximum of 20-30 minutes to each enrolled patient's visit. The iPad audiogram observations will not be used by the patient's physician for diagnostic and treatment purposes.

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Conditions studied

  • Hearing Loss

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03

In context

Hearing Loss

1,092 studies on the registry are indexed under Hearing Loss; 235 are open to participants now.

This study's planned enrollment of 120 is above the median of 87 across 270 observational studies indexed under Hearing Loss.

Browse Hearing Loss studies →

Lead sponsor

This is the only study on the registry with Matt Bromwich as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adults (> or equal to18 years) attending the ENT/Audiology clinic at The Ottawa Hospital (CIVIC Campus) will be eligible to participate.

Inclusion criteria

  • For Group I and II all adults over the age of 18 years who attend an Audiology clinic for conventional Audiometry at the Civic campus will be eligible for this study.
  • For Group III adults over the age of 18 years who attend ENT clinic but aren't undergoing conventional audiometric testing will be eligible.

Exclusion criteria

Exclusion Criteria:

  • Patients who self report being unable to play the iPad game.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
120 participants (estimated)
Patient registry
No

Groups and cohorts

  • Automated Mobile Interactive Audiometer, Test Retest

    Each participant will act as his/her own control. The iPad audiogram will be compared to the audiogram in sound booth or to a second iPad audiogram.

    Device: Automated Mobile Interactive Audiometer

  • Automated Mobile Interactive Audiometer, Validation.

    iPad testing will be compared to conventional audiometry in the sound booth.

    Device: Automated Mobile Interactive Audiometer

  • Automated Mobile Interactive Audiometer, Speech Recognition

    Testing with NU-6 word lists will be conducted by the iPad and by an audiologist in the sound booth.

    Device: Automated Mobile Interactive Audiometer

  • Automated Mobile Interactive Audiometer, Cochlear Implant

    Participants with cochlear implants will be tested using iPad against conventional audiometry (warble tone) in the sound booth.

    Device: Automated Mobile Interactive Audiometer

Interventions

  • DeviceAutomated Mobile Interactive Audiometer

    iPad game

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What researchers measure

Primary outcomes

  1. Validate the use of an iPad audiometer for hearing testing in adults aged 18 and older in Ottawa, Canada.

    iPad audiogram will be compared to conventional audiogram (sound booth) and test/retest reliability of the iPad will be measured in Group 3.

    Time frame: 8 months

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Study locations

1 of 1 sites recruiting
  • The Ottawa Hospital Civic and General Campuses
    Ottawa, Ontario K1Y 4E9, Canada
    Recruiting
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References and documents

Publications

  • Bastianelli M, Mark AE, McAfee A, Schramm D, Lefrancois R, Bromwich M. Adult validation of a self-administered tablet audiometer. J Otolaryngol Head Neck Surg. 2019 Nov 7;48(1):59. doi: 10.1186/s40463-019-0385-0. PubMed 31699157 ↗

Individual participant data

Plan to share: Undecided

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 10, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02761798
Lead sponsor
Matt Bromwich
Collaborators
Clearwater Clinical, Children's Hospital of Eastern Ontario
Responsible party
Matt Bromwich (Otolaryngologist, Head and Neck Surgeon, Ottawa Hospital Research Institute) — Sponsor-investigator
First posted
May 4, 2016
Start date
Apr 2016
Primary completion
Dec 2018 (estimated)
Completion
Dec 2018 (estimated)
Last update
Apr 10, 2018

Study contacts

Debora L Hogan, M.Sc.N.
Contact
dhogan@ohri.ca
613-737-8899 ext. 72978
David Schramm, MD
principal investigator · The Ottawa Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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