Virtual Acoustic Localization Experiment (VALEEvE)
Primary Purpose
Hearing Loss
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Oldenburger sentence test, localization test
Sponsored by
About this trial
This is an interventional other trial for Hearing Loss
Eligibility Criteria
Inclusion Criteria:
- adults , in general healthy (no diagnosis of dementia and/or stroke known), mother tongue: (swiss) german, normal hearing or with hearing aid wearers both sides or with CI support on both sides, symmetrical hearing loss
Exclusion Criteria:
- deviation of inclusion criteria, known fluctuating, rapidly progressive hearing loss, test person is not able to come one time a week to the University Hospital of Zurich or to handle 1-2 hours appointments or is not able to use touchscreen
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
dereverberation condition
reverberation condition
Arm Description
Oldenburger Sentence test, localization test
Oldenburger Sentence test, localization test
Outcomes
Primary Outcome Measures
Oldenburger sentence test and localization test with 30 subjects
The impact of a dereverberation algorithm for hearing aids and / or cochlear implants will be checked
Secondary Outcome Measures
Differences in localization ability
By VALE (localization test) can differences in the localization ability between normal hearing and hearing-impaired people be measured
Full Information
NCT ID
NCT02602171
First Posted
November 4, 2015
Last Updated
October 31, 2017
Sponsor
University of Zurich
1. Study Identification
Unique Protocol Identification Number
NCT02602171
Brief Title
Virtual Acoustic Localization Experiment
Acronym
VALEEvE
Official Title
Virtual Acoustic Localization Experiment for the Evaluation of a Dereverberation Algorithm in Terms of Speech Intelligibility & Localization Performance of Normal Hearing & Hearing Impaired Subjects
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
April 2015 (Actual)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The present study has the evaluation of a test to measure the localization performance goal . It is about the perception of danger audio signals in everyday listening environments nearby which are reproduced in controlled laboratory conditions. In addition, a dereverberation algorithm regarding speech intelligibility and localization ability is evaluated . The research hypothesis is that the dereverberation of the audio signals can improve speech intelligibility for both normal hearing and hearing-impaired persons. In addition, the binaural dereverberation algorithm should not affect the localization ability in everyday situations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Loss
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
dereverberation condition
Arm Type
Experimental
Arm Description
Oldenburger Sentence test, localization test
Arm Title
reverberation condition
Arm Type
Experimental
Arm Description
Oldenburger Sentence test, localization test
Intervention Type
Other
Intervention Name(s)
Oldenburger sentence test, localization test
Primary Outcome Measure Information:
Title
Oldenburger sentence test and localization test with 30 subjects
Description
The impact of a dereverberation algorithm for hearing aids and / or cochlear implants will be checked
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Differences in localization ability
Description
By VALE (localization test) can differences in the localization ability between normal hearing and hearing-impaired people be measured
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
adults , in general healthy (no diagnosis of dementia and/or stroke known), mother tongue: (swiss) german, normal hearing or with hearing aid wearers both sides or with CI support on both sides, symmetrical hearing loss
Exclusion Criteria:
deviation of inclusion criteria, known fluctuating, rapidly progressive hearing loss, test person is not able to come one time a week to the University Hospital of Zurich or to handle 1-2 hours appointments or is not able to use touchscreen
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norbert Dillier, Prof. Dr.
Organizational Affiliation
University of Zurich
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Virtual Acoustic Localization Experiment
We'll reach out to this number within 24 hrs