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Completed

NCT Number: NCT03512951

Subjective Evaluation of a Sound Processing Method for Hearing Aids on Auditory Distance Perception

Within the course of this study, a signal processing feature has been developed at Ecole Polytechnique Fédérale de Lausanne (EPFL), in collaboration with Sonova AG, in order to enhance the listening experience with remote microphone systems. In particular, the developed feature is supposed to improve the so-called audio-visual fusion, i.e. the fact to perceive the sound as coming from the physical location of the source. One of the main goals of the present study is to evaluate the extent to which this feature reaches that objective.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ecole Polytechnique Fédérale de Lausanne, Lausanne, Canton of Vaud, Switzerland

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Who can participate

Healthy volunteers accepted: Yes

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

Subjects fulfilling all of the following inclusion criteria are eligible for the study:

  • Willing and able to give written informed consent as documented by signature,
  • French-native adult speakers,
  • (Preferably) younger than 60 y.o.

For all normal-hearing participants:

  • Hearing thresholds lower or equal to 20 dB on both ears, as ensured by a pure-tone audiometry (125 Hz to 8 kHz) conducted at the beginning of the session.

For all hearing-impaired patients:

  • Patients of Mr. Philippe Estoppey, private audiologist settled in Lausanne,
  • User of bilateral BTE Phonak hearing aids, commercialized after July 2012, with fittings that did not change over the last three months,
  • Presenting a severe-to-profound sensorineural hearing loss,
  • Presenting a symmetrical hearing loss (no bilateral hearing threshold that differ by more than 20 dB at any audiometric frequency (125 Hz - 4 kHz)).

For HI patients experienced with remote microphone systems:

  • Past or present users of FM and/or Roger devices for more than six months.

For other HI patients:

  • No past or present experience with FM and/or Roger devices for more than one month.

The presence of any one of the following exclusion criteria will lead to exclusion of the participant:

  • Collaborator of the laboratory (LTS2) or student attending the courses of audio and acoustics given by the laboratory staff (EE-348 Electroacoustics, EE-548 Audio Engineering),
  • History of chronic or terminal illness, psychiatric disturbance, senile dementia, or cognitive impairment,
  • History of strong tinnitus and/or hyperacusis,
  • Strong visual impairment after correction with glasses or not,
  • History of epilepsy or other reactions associated with the proximity to a screen,
  • Motor disability that would disturb their presence at EPFL.

Treatment and study plan

Digital signal processing algorithms

Other

The intervention consists in applying five processing on some recorded speech signals. In particular, the processing performed by one specific algorithm is compared against the four other. The applied processing is supposed to restore sound externalization (expected audio-visual fusion).

Primary outcomes

  1. Auditory distance estimation

    Time frame: 6 months (study completion)

    This objective is assessed by using a single outcome, which is the perceived auditory distance, as reported by the patient on a graphical user interface. The auditory distance is measured using an arbitrary scale (between 1 and 5) as available with sliders on a graphical user interface (GUI).

Sponsors and collaborators

Lead sponsor

Sonova AG

Industry

Collaborators

  • David Sooprayen
  • Eleftheria Georganti
  • Gilles Courtois
  • Peter Derleth
  • Vincent Grimaldi

Registry information

Official study title

Subjective Evaluation of a Sound Externalization Method in Remote Microphone Systems for Binaural Hearing Aids With Respect to Auditory Distance Perception

Acronym: EXTEND

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
May 1, 2018
Registry last updated
Dec 20, 2018

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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