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Study of SelfFit Mobile Medical App for Hearing Loss Diagnostics and Hearing Device Fitting / Fine Tuning (SelfFit)

Primary Purpose

Mild to Moderate Sensorineural Hearing Loss

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
SelfFit adjusted hearing device
Sponsored by
Two Pi Signalprocessing Applications GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Mild to Moderate Sensorineural Hearing Loss focused on measuring Audiology, hearing loss, hearing healthcare, mobile app, hearing aid fitting, audiometry, audiogram

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Hearing loss at the better ear between 35dB and 50dB (PTA1/2/4)
  • Active lifestyle
  • No language problems
  • No medical contra-indications
  • Age: between 18 and 75 years
  • About 50% experienced users and 50% new users
  • Willing to participate in the trial with one three hour visit to the AMC.

Exclusion Criteria:

  • Conductive hearing loss in the middle ear
  • Severe hearing loss

Sites / Locations

  • Department of Clinical & Experimental Audiology of the Academic Medical Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

SelfFit adjusted hearing device

Arm Description

Hearing impaired people with mild to moderate sensorineural hearing loss (PTA124<50 dB) in the test ear compare the performance of their hearing aids adjusted through SelfFit mobile medical App (I-Pad) with the performance of their hearing aids adjusted through conventional audiogram-based fitting.

Outcomes

Primary Outcome Measures

Hearing threshold
Applicability of in-situ audiometry: Comparison of pure tone audiometry outcomes: conventional full diagnositic and SelfFit in-situ audiometry

Secondary Outcome Measures

Speech intelligibility - First Fit
Quality of First-Fit: Comparison speech audiometry with CVC words @ 55/65/75 db SPL in conventionally adjusted hearing aid and SelfFit adjusted hearing aid

Full Information

First Posted
May 28, 2013
Last Updated
October 21, 2016
Sponsor
Two Pi Signalprocessing Applications GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT01877317
Brief Title
Study of SelfFit Mobile Medical App for Hearing Loss Diagnostics and Hearing Device Fitting / Fine Tuning
Acronym
SelfFit
Official Title
Study of SelfFit App for Hearing Loss Diagnostics Based on Threshold Measurements Through In-situ Audiometry and Adjustment of Hearing Device Amplification Parameters in Agreement With Prescriptive Formulas as NAL-NL1,DSL-i/o
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
May 2013 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
August 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Two Pi Signalprocessing Applications GmbH

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this clinical study is to validate the comparability of prescription formula fitting of hearing aids based on full diagnostic audiometry and SelfFit interactive fitting of hearing aids based on hearing loss screening (mild to moderate hearing losses) using in-situ audiometry, provided and executed through the mobile medical app.
Detailed Description
The technology utilized within the mobile medical App is partially described in the US patent application US2011/0002490A1. The app is to be used in combination with a hearing aid to deliver the output and targets accurate individual acoustical amplification for effective compensation of a users hearing loss. The electronic circuitry incorporating the digital signal processing algorithms - dynamic range compression, noise reduction - is providing the acoustical amplification according to parameters (acoustical gain, compression ratio, time constants) calculated through the App on base of in-situ hearing loss diagnostics (pure tone audiometry, loudness scaling). Within the study, amplification parameters will be transmitted to the prototyped device through a prototyped audio streaming box. Individual audiogram represents hearing thresholds (softest audible sounds) at different frequencies. At least two test frequencies are used involving one in the lower region of device's bandwidth (such as 750 Hz) and one in the higher region of the device's bandwidth (such as 2 kHz). Hearing thresholds are assessed by presenting pure tones of different known levels (SPL) to the user and the thresholds for each of the test frequencies are determined according to the user response to a verbally formulated question (how many tones did you hear?) and multiple choice answer buttons (0, 1, or 2). Second hearing loss characteristic obtained by the app. is the personal loudness scaling. By presenting a band-limited noise stimuli and collecting the user response about perceived loudness level Medical Mobile App calculates dynamic range of users hearing at given frequency. The calculation of optimal amplification parameters is performed by App using a proprietary "fitting formula" derived from scientific data. Final adjustment of amplification parameters called fine tuning is performed while presenting the user with realistic acoustical environment during operation of the hearing device. Fine tuning relates to slight changes of the parameters initially obtained by the "fitting formula". The acoustical signals are presented using audio streaming through the hearing aid. In particular the presented signals include "speech in quiet" and "speech in background noise". Presented speech signal is composed from two or more sources that are processed with different signal processing parameters. During the presentation of the speech signal App presents the speech source visually as two or more speakers. The user is asked to provide his listening preference by choosing the preferred speaker. The signal processing parameters relating to the preferred sound are used for final adjustment of hearing device.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild to Moderate Sensorineural Hearing Loss
Keywords
Audiology, hearing loss, hearing healthcare, mobile app, hearing aid fitting, audiometry, audiogram

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
SelfFit adjusted hearing device
Arm Type
Experimental
Arm Description
Hearing impaired people with mild to moderate sensorineural hearing loss (PTA124<50 dB) in the test ear compare the performance of their hearing aids adjusted through SelfFit mobile medical App (I-Pad) with the performance of their hearing aids adjusted through conventional audiogram-based fitting.
Intervention Type
Device
Intervention Name(s)
SelfFit adjusted hearing device
Other Intervention Name(s)
User-fitted hearing device, hearing device fitting software, home-fitting tool for hearing devices
Intervention Description
Comparison of threshold measurements through in-situ audiometry with full diagnostic audiometry; Comparison of First-Fit based on SelfFit-formula with conventional fitting formula NAL-NL1 (IG-measurements; Speech intelligibility with First fit of SelfFit; Speech intelligibility with Final fit of SelfFit; Comparison of fine tuning through SelfFit (Final fit) with First fit; Comparison of Final fit with Traditional fit (conventional fitted hearing aid of the test person)
Primary Outcome Measure Information:
Title
Hearing threshold
Description
Applicability of in-situ audiometry: Comparison of pure tone audiometry outcomes: conventional full diagnositic and SelfFit in-situ audiometry
Time Frame
June - July 2013 (up to 2 months)
Secondary Outcome Measure Information:
Title
Speech intelligibility - First Fit
Description
Quality of First-Fit: Comparison speech audiometry with CVC words @ 55/65/75 db SPL in conventionally adjusted hearing aid and SelfFit adjusted hearing aid
Time Frame
June - July 2013 (up to 2 months)
Other Pre-specified Outcome Measures:
Title
Speech intelligibility - Final Fit
Description
Quality of Final-Fit: Comparison speech audiometry with CVC words @ 55/65/75 db SPL in conventionally adjusted hearing aid and SelfFit adjusted hearing aid
Time Frame
June - July 2013 (up to 2 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Hearing loss at the better ear between 35dB and 50dB (PTA1/2/4) Active lifestyle No language problems No medical contra-indications Age: between 18 and 75 years About 50% experienced users and 50% new users Willing to participate in the trial with one three hour visit to the AMC. Exclusion Criteria: Conductive hearing loss in the middle ear Severe hearing loss
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wouter A Dreschler, Prof.dr.ir.
Organizational Affiliation
Department of Clinical & Experimental Audiology of the Academic Medical Centre in Amsterdam
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Clinical & Experimental Audiology of the Academic Medical Centre
City
Amsterdam
ZIP/Postal Code
1105 AZ
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Study of SelfFit Mobile Medical App for Hearing Loss Diagnostics and Hearing Device Fitting / Fine Tuning

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