Morphology Effects of Extended Wear Hearing Instrument
Primary Purpose
Hearing Loss
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Morphology changes with extended wear hearing aid
Sponsored by
About this trial
This is an interventional basic science trial for Hearing Loss focused on measuring hearing loss, hearing aid
Eligibility Criteria
Inclusion Criteria:
- Adult patients in the USC Otolaryngology Clinic who are determined to be candidates for a Lyric extended wear hearing aid device by their treating Audiologist (in general people with mild to moderate hearing loss may be eligible).
Exclusion Criteria:
- Patients in the USC Clinic who are determined by the Audiologist not to be good candidates for the Hearing aid extended wear device (in general, people with severe hearing loss are not eligible).
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Hearing Aid
Arm Description
Actual Patients in the clinic will be evaluated by their Audiologist, if they are candidates to use the Lyric Hearing aid they will be asked if they want to participate in the study which will include imaging of the ear canal with a device similar to the regular ear device used in the clinic to check if there are any changes to the morphology of the ear canal.
Outcomes
Primary Outcome Measures
Morphology imaging
Imaging of the tissue at each appointment will be made
Secondary Outcome Measures
Full Information
NCT ID
NCT03902093
First Posted
April 1, 2019
Last Updated
December 6, 2021
Sponsor
University of Southern California
1. Study Identification
Unique Protocol Identification Number
NCT03902093
Brief Title
Morphology Effects of Extended Wear Hearing Instrument
Official Title
Longitudinal Study of External Auditory Canal Morphology With Regards to Extended-wear Hearing Instrument
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Withdrawn
Why Stopped
Study is withdrawn due to no enrollment, due to COVID pandemic.
Study Start Date
August 1, 2022 (Anticipated)
Primary Completion Date
February 1, 2023 (Anticipated)
Study Completion Date
June 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The lyric hearing device is a commercially available device produced by Sonova, and designed to be used for extended periods of time. We further want to investigate the morphology of the tissue around the device at different periods of time after the device has been fitted and used for a while.
An initial imaging of the tissue will be taken for baseline measurements. Questionnaires will also be used to assess patients satisfaction with the device and cognitive abilities.
Detailed Description
If the person seems to be a good candidate for the study, the Audiologist could discuss with the patient the time involved in the study and arrange an appointment with the patient if interested.
A series of appointments are designed to follow up the patient's development with the device at determined times during the process. On the first appointment the patient will be consented prior to any tests or health services given.
The first and last appointments are the longest ones with a duration of about 1 and a half hours for questionnaires, medical history, and device fitting. Additionally, all appointments include measurement of ear canal relative humidity which should take a total of 30 minutes and imaging of the area to determine thickness and blood flow in the tissue surrounding the device. Follow-up appointments with the Audiologist will take 45 minutes for all basic procedures. The Lyric device is used commercially and Audiologist can provide it to patients already, but the purpose of this study is to use a pioneer technique with a device that looks inside the ear canal in the same way as a regular used speculum to look at details of the tissue around the device to see if any changes occur due to extended wear of the Lyric hearing aid device.
The complete study per person will be completed in about six months. An Audiologist will perform all the audiology testing plus the ear canal humidity measurements and his/her time will be covered by the sponsor (a total of 9 hours per patient). The Lyric devices will be provided on loan by the sponsor as well as the equipment and software needed to make the ear canal humidity measurements. The imaging measurements will be conducted by the Audiologist trained in using the handheld device.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Loss
Keywords
hearing loss, hearing aid
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hearing Aid
Arm Type
Experimental
Arm Description
Actual Patients in the clinic will be evaluated by their Audiologist, if they are candidates to use the Lyric Hearing aid they will be asked if they want to participate in the study which will include imaging of the ear canal with a device similar to the regular ear device used in the clinic to check if there are any changes to the morphology of the ear canal.
Intervention Type
Diagnostic Test
Intervention Name(s)
Morphology changes with extended wear hearing aid
Intervention Description
Possible changes in morphology due to wearing an extended wear hearing aid device will be assessed with imaging
Primary Outcome Measure Information:
Title
Morphology imaging
Description
Imaging of the tissue at each appointment will be made
Time Frame
Complete study will take about six months per person
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Adult patients in the USC Otolaryngology Clinic who are determined to be candidates for a Lyric extended wear hearing aid device by their treating Audiologist (in general people with mild to moderate hearing loss may be eligible).
Exclusion Criteria:
Patients in the USC Clinic who are determined by the Audiologist not to be good candidates for the Hearing aid extended wear device (in general, people with severe hearing loss are not eligible).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kristina Rousso, AuD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Morphology Effects of Extended Wear Hearing Instrument
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