Hearing Aid Noise Reduction in Pediatric Users (Oticon Study) (OtiS)
Primary Purpose
Hearing Impairment, Hearing Loss, Sensorineural
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Oticon OpenSound Navigator speech enhancement algorithm
Oticon omni-directional microphone algorithm
Sponsored by
About this trial
This is an interventional treatment trial for Hearing Impairment
Eligibility Criteria
Inclusion Criteria:
- children ages 6 to 13 years
- English as the primary home language
- positive for bilateral symmetrical mild to moderately-severe sensorineural hearing loss
- currently using hearing aids that were dispensed at least 18 months prior to enrollment of the study
- negative for major cognitive handicap or developmental delay that would prevent or restrict participation, as determined by the PI or designee
- negative for learning disability, for example attention-deficit/hyperactivity disorder, as determined by the PI or designee
- negative for serious neurological or psychiatric disease that would prevent or restrict participation, as determined by the PI or designee
- informed consent of parent/guardian
- assent of participating child if aged 11 years and over
- standard MRI inclusion criteria as set by the Cincinnati Children's Hospital Medical Center department of Radiology
- not currently pregnant or breast feeding
- willingness and ability of the participant and/or the participant's caregiver to comply with study requirements
- no history of medical neglect of caregiver
Sites / Locations
- Cincinnati Children's Hospital Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
OpenSound Navigator (OSN) Hearing Aid
omni-directional Hearing Aid
Arm Description
Participants will be fit with Oticon OPN™ behind-the-ear hearing aids with the OpenSound Navigator algorithm enabled. Participants are to use the hearing aids at least an average of 8 hours per day over the course of 6-8 months.
Participants will be fit with Oticon OPN™ behind-the-ear hearing aids with the Omni-directional microphone system enabled. Participants are to use the hearing aids at least an average of 8 hours per day over the course of 6-8 months.
Outcomes
Primary Outcome Measures
Change from Baseline Word Recognition Abilities at 6 to 8 Months
Aided speech perception in noise within a week of hearing aid fitting and again 6-8 months later.
Secondary Outcome Measures
Change from Baseline Speech, Spatial Qualities of Hearing Scale (SSQ) Scores at 6 to 8 Months
Speech, Spatial and Qualities of Hearing Scale (SSQ), a survey utilizing an ordinal scale specifically measuring hearing aid benefit with regard to speech understanding, spatial awareness, perceptual quality of sound, and conversation, will be completed by parents/legal guardian within a week of the hearing aid fitting and after wearing the study hearing aids for 6-8 months. There are 4 survey sections. Section A: Speech has 8 questions, Section B: Spatial Hearing has 5 questions, Section C: Qualities of Hearing has 8 questions and Section D: Conversational Uses of Hearing has 5 questions. Each question uses a scale ranging from 0 (poorest possible outcome) to 100 (best possible outcome). Each section calculates an average score across the corresponding questions for a total of 4 individual scores.
Hearing aid use time
Average daily use of hearing aids.
Full Information
NCT ID
NCT03771287
First Posted
November 27, 2018
Last Updated
December 18, 2020
Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Oticon
1. Study Identification
Unique Protocol Identification Number
NCT03771287
Brief Title
Hearing Aid Noise Reduction in Pediatric Users (Oticon Study)
Acronym
OtiS
Official Title
Learning to Listen in Noise: A Double-blind Randomized Control Trial of a New Hearing Aid Noise Reduction System
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
December 5, 2018 (Actual)
Primary Completion Date
July 30, 2020 (Actual)
Study Completion Date
August 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Oticon
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the efficacy of OpenSound Navigator (OSN), a hearing aid speech-enhancement algorithm developed by Oticon, as treatment for pediatric hearing aid users. Using a double-blind experimental design, the investigators aim to compare two treatment groups of pediatric (ages 6-12) patients with symmetrical sensorineural hearing losses ranging from the mild to moderately-severe degree. One group will be fit with bilateral Oticon OPN™ behind-the-ear hearing aids set with an omni-directional microphone setting. The other group will be fit with the same hearing aid model with the OSN algorithm enabled. Participants from the groups will be age and audiogram-matched. The investigators will evaluate hearing aid benefit through word recognition in noise (behavioral testing) and everyday hearing/listening abilities (parental/legal guardian reported) at hearing aid fitting and 6-8 months post fitting.
Detailed Description
OpenSound Navigator (OSN) is a speech enhancement hearing aid algorithm developed by Oticon that utilizes an adaptive directional microphone system with an automatic gain control noise reduction program. This hearing aid feature is intended for adult hearing aid users and its potential benefits of speech, vocabulary and listening development in pediatric users has not been investigated. Here the investigators aim to evaluate the efficacy of OSN programming in pediatric hearing aid users (6-12 years of age) diagnosed with a symmetrical sensorineural hearing loss in the mild to moderately-severe range. The investigators will use a double-blind randomized control methodology of two participant matched (based on age and audiometric configuration) groups. The first group will include pediatric patients fit with bilateral Oticon OPN™ behind-the-ear hearing aids with the standard Omni-directional microphone setting enabled. Group two will include pediatric patients fit with the same hearing aid model with the OSN feature enabled. Participants will undergo standard audiometric diagnostic testing and will be fit with the hearing aids by a licensed clinical audiologist. Participants are required to wear the hearing aids full time (at least 8 hours per day average) during the duration of the study. The evaluation measures will include speech recognition testing in controlled background noise and the Speech, Spatial and Qualities of Hearing Scale questionnaire (completed by parents/legal guardian). Testing will be performed within a week of the hearing aid fitting and 6-8 months post fitting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Impairment, Hearing Loss, Sensorineural
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
Double-blinded randomized control trial of OpenSound Navigator (OSN) enabled/disabled hearing aids. Only the fitting audiologist will know if the OSN algorithm is enabled or disabled in the research hearing aids. Will be un-blinded after data collection is complete in order to carry out group comparison analysis.
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
OpenSound Navigator (OSN) Hearing Aid
Arm Type
Experimental
Arm Description
Participants will be fit with Oticon OPN™ behind-the-ear hearing aids with the OpenSound Navigator algorithm enabled. Participants are to use the hearing aids at least an average of 8 hours per day over the course of 6-8 months.
Arm Title
omni-directional Hearing Aid
Arm Type
Active Comparator
Arm Description
Participants will be fit with Oticon OPN™ behind-the-ear hearing aids with the Omni-directional microphone system enabled. Participants are to use the hearing aids at least an average of 8 hours per day over the course of 6-8 months.
Intervention Type
Device
Intervention Name(s)
Oticon OpenSound Navigator speech enhancement algorithm
Other Intervention Name(s)
OSN
Intervention Description
OpenSound Navigator (OSN) is a speech enhancement algorithm developed by Oticon. The feature is built in Oticon's current OPN™ hearing aid platform and can be adjusted and disabled in the programming. It is designed to automatically enhance speech while reducing unwanted background noise to improve communication for the user.
Intervention Type
Device
Intervention Name(s)
Oticon omni-directional microphone algorithm
Other Intervention Name(s)
omni-directional mic
Intervention Description
Omni-directional microphone setups come standard for all Oticon hearing aid models. The hearing microphones have equal sensitivity across all directions.
Primary Outcome Measure Information:
Title
Change from Baseline Word Recognition Abilities at 6 to 8 Months
Description
Aided speech perception in noise within a week of hearing aid fitting and again 6-8 months later.
Time Frame
6-8 months
Secondary Outcome Measure Information:
Title
Change from Baseline Speech, Spatial Qualities of Hearing Scale (SSQ) Scores at 6 to 8 Months
Description
Speech, Spatial and Qualities of Hearing Scale (SSQ), a survey utilizing an ordinal scale specifically measuring hearing aid benefit with regard to speech understanding, spatial awareness, perceptual quality of sound, and conversation, will be completed by parents/legal guardian within a week of the hearing aid fitting and after wearing the study hearing aids for 6-8 months. There are 4 survey sections. Section A: Speech has 8 questions, Section B: Spatial Hearing has 5 questions, Section C: Qualities of Hearing has 8 questions and Section D: Conversational Uses of Hearing has 5 questions. Each question uses a scale ranging from 0 (poorest possible outcome) to 100 (best possible outcome). Each section calculates an average score across the corresponding questions for a total of 4 individual scores.
Time Frame
6-8 months
Title
Hearing aid use time
Description
Average daily use of hearing aids.
Time Frame
6-8 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
children ages 6 to 13 years
English as the primary home language
positive for bilateral symmetrical mild to moderately-severe sensorineural hearing loss
currently using hearing aids that were dispensed at least 18 months prior to enrollment of the study
negative for major cognitive handicap or developmental delay that would prevent or restrict participation, as determined by the PI or designee
negative for learning disability, for example attention-deficit/hyperactivity disorder, as determined by the PI or designee
negative for serious neurological or psychiatric disease that would prevent or restrict participation, as determined by the PI or designee
informed consent of parent/guardian
assent of participating child if aged 11 years and over
standard MRI inclusion criteria as set by the Cincinnati Children's Hospital Medical Center department of Radiology
not currently pregnant or breast feeding
willingness and ability of the participant and/or the participant's caregiver to comply with study requirements
no history of medical neglect of caregiver
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David R Moore, Ph.D.
Organizational Affiliation
Children's Hospital Medical Center, Cincinnati
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35758427
Citation
Stewart HJ, Cash EK, Pinkl J, Nakeva von Mentzer C, Lin L, Hunter LL, Moore DR; CCHMC Division of Audiology. Adaptive Hearing Aid Benefit in Children With Mild/Moderate Hearing Loss: A Registered, Double-Blind, Randomized Clinical Trial. Ear Hear. 2022 Sep-Oct 01;43(5):1402-1415. doi: 10.1097/AUD.0000000000001230. Epub 2022 Jun 27.
Results Reference
derived
Learn more about this trial
Hearing Aid Noise Reduction in Pediatric Users (Oticon Study)
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