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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05274178
Other study ID # SRF-505
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 26, 2022
Est. completion date June 16, 2022

Study information

Verified date June 2023
Source Sonova AG
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

New and experienced hearing aid users will be fit with two hearing devices. One will be labeled as an OTC (Over-The-Counter) device, the other will be labeled as a Prescriptive (i.e. professionally fit) device. Both devices will be generically programmed for a mild to moderate hearing loss. An objective speech in noise test will be completed with both devices.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 16, 2022
Est. primary completion date June 16, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria: - Adults age 18 or older with bilateral mild to moderate hearing loss - Experienced users must have at least 6 months Hearing Aid experience - New users must have no prior hearing aid experience, defined as never owning their own devices Exclusion Criteria: - Self-reported ear related pathology (otorrhea w/in 90 days, dizziness, sudden hearing loss or worsening of hearing w/in 90 days, otalgia) - Visible deformity of the ear - Chronic, severe tinnitus - Unilateral hearing loss - Cognitive impairment

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Audeo P hearing aid labeled as "Prescriptive"
The Audeo P is a commercially available hearing aid that is fit by a hearing care professional. The devices will be labeled as "prescriptive" in view of the participant.
Audeo P hearing aid labeled as "OTC"
The Audeo P is a commercially available hearing aid that is fit by a hearing care professional. The devices will be labeled as "OTC" in view of the participant.

Locations

Country Name City State
United States Sonova US Aurora Illinois

Sponsors (1)

Lead Sponsor Collaborator
Sonova AG

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quick Speech in Noise Test (QuickSIN) A speech in noise test in which participant repeats sentences in variable levels of background noise. Test result is reported as the signal to noise level at which participant can repeat 50% of the words correctly. A lower score/dB SNR (decibel Signal to Noise Ratio) level indicates better speech in noise perception. For example, a score of 0 dB would indicate that the participant can repeat 50% of the words presented when the speech signal and the noise are presented at the same level. A score of 6 dB would indicate that the participant needs the speech signal 6 dB louder than the noise in order to correctly repeat 50% of the words presented. Scores can range from negative db SNR (e.g. -5 dB, which would be a good score and indicate little difficulty in noise) to quite high (e.g. +15 dB, which would be a poorer score and indicate much difficulty in noise) In this case, the scores ranged from +2 to +18 dB. Day 1 of 1 day study
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