search
Back to results

Improving Access and Affordability of Adult Hearing Healthcare

Primary Purpose

Hearing Loss

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Hearing Evaluation
Personal Sound Amplification Product (PSAP) Fitting and Orientation
Four Weeks of Aural Rehabilitation
Provision of Personal Sound Amplification Products (PSAPs)
Sponsored by
University of Alabama, Tuscaloosa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hearing Loss

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Mild-to-moderate hearing loss
  • Live in West Central or South Alabama
  • 40 years of age or older

Exclusion Criteria:

โ€ข Medical conditions resulting in severe cognitive impairment (e.g., stroke, head injury, senile dementia or Alzheimer's disease)

Sites / Locations

  • The University of AlabamaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Active Comparator

Arm Label

Audiology Best Practices plus Aural Rehabilitation (ABP+AR)

Audiology Best Practices (ABP)

Over-the-Counter Only (OTC-Only)

Arm Description

This experimental group will receive a hearing evaluation, an over-the-counter hearing aid fitting and orientation, and four-weeks of an aural rehabilitation program conducted by specially-trained community health workers. Additionally, these adults will complete pre- and post-questionnaires and speech perception testing.

This comparison group of adults with hearing loss will receive a hearing evaluation and over-the-counter hearing aid fitting and orientation. The aural rehabilitation program will not be provided initially. These participants will complete pre- and post-questionnaires and speech perception testing.

This comparison group of adults with hearing loss will receive a hearing evaluation. They will be provided with over-the-counter hearing aids but the audiologist will not assist with fitting the aids or providing an orientation. This arm mimics what would happen when a consumer privately purchases over-the-counter hearing aids. They will complete pre- and post-questionnaires and speech perception testing.

Outcomes

Primary Outcome Measures

Measuring Change in the Hearing Handicap Inventory for Elderly (HHIE) Outcomes
Twenty-five questions of the Hearing Handicap Inventory for Elderly (HHIE) measure emotional and social/situational consequences of hearing loss, including feelings of embarrassment, social isolation, and frustration. Scores range from 0 to 100 with higher scores indicative of poorer performance.
Measuring Change in International Outcome Inventory for Hearing Aids (IOI-HA) Outcomes
The International Outcome Inventory for Hearing Aids (IOI-HA) is an eight-item inventory that assesses daily use of over-the-counter hearing aid use, over-the-counter hearing aid benefit, and activity limitations to name a few. This is a scaled qualitative measure that assesses outcomes over time.

Secondary Outcome Measures

Measuring Change in Northwestern University-6 (NU-6) Word Recognition Outcomes
This test will assess word recognition in quiet. Binaural testing will be performed at 65 dBA in the sound field. A percentage correct word understanding will be obtained. A higher scores is indicative of better performance.
Measuring Change in Quick Speech In Noise (SIN) Word Recognition Outcomes
The participant will be instructed to repeat the presented sentences in noise via a speaker presented at 0หš azimuth. The correctly identified target words will be totaled and then subtracted from 25.5 to obtain the Signal-to-Noise Ratio (SNR) loss. A higher score is indicative of poorer performance.
Measuring Change in the Client Oriented Scale of Improvement (COSI)
The Client Oriented Scale of Improvement (COSI) is a 16-item clinician-administered survey that addresses how the participants' five most important listening difficulties have been alleviated with over-the-counter hearing aid use. This is a qualitative scale that measures improvement over time.
Measuring Change in the Abbreviated Profile of Hearing Aid Benefit (APHAB)
The Abbreviated Profile of Hearing Aid Benefit (APHAB) is a 24-item survey that computes PSAP-benefit by calculating the difference between aided and unaided conditions. It is a qualitative scale that measures the extent of change over time.
Measuring Change in the World Health Organization Quality of Life-Age (WHOQOL-AGE) Survey
The World Health Organization Quality of Life-Age (WHOQOL-AGE) survey is a 13-item scale that examines quality of life in adults as they age. It is a qualitative rating scale that can help to identify change in performance over time.

Full Information

First Posted
December 3, 2020
Last Updated
June 29, 2023
Sponsor
University of Alabama, Tuscaloosa
Collaborators
University of Alabama at Birmingham
search

1. Study Identification

Unique Protocol Identification Number
NCT04671381
Brief Title
Improving Access and Affordability of Adult Hearing Healthcare
Official Title
Improving Access and Affordability of Adult Hearing Healthcare: Effectiveness of Community-based Interventions in West Central and South Alabama
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alabama, Tuscaloosa
Collaborators
University of Alabama at Birmingham

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.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This project will address quality of care issues associated with hearing loss in adults who have mild-to-moderate hearing loss and who have no access to hearing healthcare. Through the use of three different interventions involving personal sound amplification products (PSAPs), it will lead to options that will increase access and affordability of hearing healthcare for adults with mild-to-moderate hearing loss.
Detailed Description
The design for this study is outlined below according to each Aim. Aim 1: To identify the effectiveness of personal sound amplification products (PSAPs) for decreasing hearing handicap and improving speech perception in adults with no access to hearing health care. Aim 2: To implement an adult aural rehabilitation (AR) program for those without access to hearing health care to improve PSAP benefit, promote PSAP use and lead to increased quality of life (QOL). Aim 1 will assess the effectiveness of over-the-counter (OTC) PSAPs for our participant population and Aim 2 will implement an AR program. With Aim 1, hearing loss will be assessed and a PSAP will be provided. Prior to the hearing evaluation, participants will be randomly placed in one of three groups to assess the effectiveness of the AR program (Aim 2). The three groups include those who will receive the current best practices care from an audiologist (ABP), those who will receive the ABP plus an aural rehabilitation program (ABP+AR), and finally, those who will receive only an OTC PSAP without assistance from an audiologist for providing programming, maintenance or care information (OTC-only). Both the ABP and OTC-only groups initially will attend general health information sessions in-place of the AR program. Local health care providers who have training in general health areas such as nutrition, diabetes, obesity, and heart health to name a few, will provide the General Health and Wellness programming. Once the ABP+AR groups have completed their AR sessions, the ABP and the OTC-only groups will attend the AR programming sessions. This testing layout and schedule is provided in the table below. Randomization will occur for each county visited and for the participants. Specifically, five counties will each receive a code and these codes will be randomized to determine when the study will take place in that area. All five regions will be included over a one-year period. Participant randomization will occur by generating three groups of random participant numbers and then assigning each participant to their designated group. Only the PI and the project manager will have access to the randomization lists. The PI will generate the randomization lists and the Project Manager will assign the participants accordingly to each group. The randomization lists will be kept on a password-protected computer and only accessible by the PI or Project Manager. Audiologists will be blinded to the intervention condition for participants. Specifically, two audiologists (A1 and A2) will conduct the initial hearing evaluations. A2 will perform the PSAP orientations and a third audiologist (A3) will perform the follow-up speech perception testing in weeks 8 - 9. Speech testing will occur before a second real ear session and PSAP adjustments are made to individual devices. Finally, the second post-speech perception testing for all participants in week 14 will be conducted by A1. The entire program will take place over a 14-week period for one county at a time. County 1 will begin at Week 1 and the remaining four regions will be stratified such that testing will begin at Week 9, 10 or 11 consecutively for each region. The stratification will be done to ensure that testing takes place in each area over a one-year period, and also, to avoid simultaneous testing at two sites. Finally, all participants who complete the study in years 1 and 2 will be invited back to complete speech perception testing and the AR surveys one year after they complete the study.

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
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Prior to the hearing evaluation, participants will be randomly placed in one of three groups. The three groups include those who will receive the current best practices care from an audiologist (ABP), those who will receive the ABP plus an aural rehabilitation program (ABP+AR), and finally, those who will receive only an OTC PSAP without assistance from an audiologist for providing programming, maintenance or care information (OTC-only). The AR programming will be provided by trained Community Health Advisors (CHAs). Both the ABP and OTC-only groups initially will attend general health information sessions in-place of the AR program. Once the ABP+AR groups have completed their AR sessions, the ABP and the OTC-only groups will attend the AR programming sessions. By using this service-delivery model, it will be possible to analyze the effectiveness of the AR programming, separate from any benefits that might occur simply by meeting with others in a group setting.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
Participant randomization will occur by generating three groups of random participant numbers and then assigning each participant to their designated group. Only the PI and the project manager will have access to the randomization lists. The PI will generate the randomization lists and the Project Manager will assign the participants accordingly to each group. Audiologists will be blinded to the intervention condition for participants. Specifically, two audiologists (A1 and A2) will conduct the initial hearing evaluations. A2 will perform the PSAP orientations and a third audiologist (A3) will perform the follow-up speech perception testing.
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Audiology Best Practices plus Aural Rehabilitation (ABP+AR)
Arm Type
Experimental
Arm Description
This experimental group will receive a hearing evaluation, an over-the-counter hearing aid fitting and orientation, and four-weeks of an aural rehabilitation program conducted by specially-trained community health workers. Additionally, these adults will complete pre- and post-questionnaires and speech perception testing.
Arm Title
Audiology Best Practices (ABP)
Arm Type
Active Comparator
Arm Description
This comparison group of adults with hearing loss will receive a hearing evaluation and over-the-counter hearing aid fitting and orientation. The aural rehabilitation program will not be provided initially. These participants will complete pre- and post-questionnaires and speech perception testing.
Arm Title
Over-the-Counter Only (OTC-Only)
Arm Type
Active Comparator
Arm Description
This comparison group of adults with hearing loss will receive a hearing evaluation. They will be provided with over-the-counter hearing aids but the audiologist will not assist with fitting the aids or providing an orientation. This arm mimics what would happen when a consumer privately purchases over-the-counter hearing aids. They will complete pre- and post-questionnaires and speech perception testing.
Intervention Type
Behavioral
Intervention Name(s)
Hearing Evaluation
Intervention Description
Behavioral thresholds for pure tones will be conducted along with speech perception measures.
Intervention Type
Device
Intervention Name(s)
Personal Sound Amplification Product (PSAP) Fitting and Orientation
Other Intervention Name(s)
Over-the-Counter Hearing Aid Fitting and Orientation
Intervention Description
Study participants will be fitted with binaural PSAPs in addition to receiving information on how to use and care for their devices.
Intervention Type
Behavioral
Intervention Name(s)
Four Weeks of Aural Rehabilitation
Intervention Description
Participants will receive four weeks of information sessions to help them adjust to their over-the-counter hearing aid and their hearing loss.
Intervention Type
Device
Intervention Name(s)
Provision of Personal Sound Amplification Products (PSAPs)
Other Intervention Name(s)
Provision of Over-the Counter Hearing Aids
Intervention Description
Study participants will receive binaural PSAPs. Participants will fit their PSAPs based on manufacturer guidelines without the help of an audiologist.
Primary Outcome Measure Information:
Title
Measuring Change in the Hearing Handicap Inventory for Elderly (HHIE) Outcomes
Description
Twenty-five questions of the Hearing Handicap Inventory for Elderly (HHIE) measure emotional and social/situational consequences of hearing loss, including feelings of embarrassment, social isolation, and frustration. Scores range from 0 to 100 with higher scores indicative of poorer performance.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 4 to 7 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.
Title
Measuring Change in International Outcome Inventory for Hearing Aids (IOI-HA) Outcomes
Description
The International Outcome Inventory for Hearing Aids (IOI-HA) is an eight-item inventory that assesses daily use of over-the-counter hearing aid use, over-the-counter hearing aid benefit, and activity limitations to name a few. This is a scaled qualitative measure that assesses outcomes over time.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 4 to 7 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.
Secondary Outcome Measure Information:
Title
Measuring Change in Northwestern University-6 (NU-6) Word Recognition Outcomes
Description
This test will assess word recognition in quiet. Binaural testing will be performed at 65 dBA in the sound field. A percentage correct word understanding will be obtained. A higher scores is indicative of better performance.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 8 to 9 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.
Title
Measuring Change in Quick Speech In Noise (SIN) Word Recognition Outcomes
Description
The participant will be instructed to repeat the presented sentences in noise via a speaker presented at 0หš azimuth. The correctly identified target words will be totaled and then subtracted from 25.5 to obtain the Signal-to-Noise Ratio (SNR) loss. A higher score is indicative of poorer performance.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 8 to 9 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.
Title
Measuring Change in the Client Oriented Scale of Improvement (COSI)
Description
The Client Oriented Scale of Improvement (COSI) is a 16-item clinician-administered survey that addresses how the participants' five most important listening difficulties have been alleviated with over-the-counter hearing aid use. This is a qualitative scale that measures improvement over time.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 4 to 7 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.
Title
Measuring Change in the Abbreviated Profile of Hearing Aid Benefit (APHAB)
Description
The Abbreviated Profile of Hearing Aid Benefit (APHAB) is a 24-item survey that computes PSAP-benefit by calculating the difference between aided and unaided conditions. It is a qualitative scale that measures the extent of change over time.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 4 to 7 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.
Title
Measuring Change in the World Health Organization Quality of Life-Age (WHOQOL-AGE) Survey
Description
The World Health Organization Quality of Life-Age (WHOQOL-AGE) survey is a 13-item scale that examines quality of life in adults as they age. It is a qualitative rating scale that can help to identify change in performance over time.
Time Frame
A baseline outcome will be obtained prior to over-the-counter hearing aid fitting. Outcomes will be measured at weeks 4 to 7 of intervention, during week 14 of the intervention, and through study completion, or 1 assessment each year.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Mild-to-moderate hearing loss Live in West Central or South Alabama 40 years of age or older Exclusion Criteria: โ€ข Medical conditions resulting in severe cognitive impairment (e.g., stroke, head injury, senile dementia or Alzheimer's disease)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marcia J Hay-McCutcheon, PhD
Phone
205-348-4572
Email
mhaymccu@ua.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcia J Hay-McCutcheon, PhD
Organizational Affiliation
The University of Alabama, Tuscaloosa
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Alabama
City
Tuscaloosa
State/Province
Alabama
ZIP/Postal Code
35487
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marcia J Hay-McCutchoen, PhD
Phone
205-348-4572
Email
mhaymccu@ua.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All of the individual participant data that has been collected during this clinical trial and after it has been de-identified will be shared.
IPD Sharing Time Frame
Data will be available beginning 3 months following article publication and ending 5 years after the article has been published.
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal will be given access to the data.
Citations:
PubMed Identifier
5296571
Citation
Tillman TW, Carhart R. An expanded test for speech discrimination utilizing CNC monosyllabic words. Northwestern University Auditory Test No. 6. SAM-TR-66-55. Tech Rep SAM-TR. 1966 Jun:1-12. doi: 10.21236/ad0639638. No abstract available.
Results Reference
result
PubMed Identifier
7095322
Citation
Schow RL, Nerbonne MA. Communication screening profile: use with elderly clients. Ear Hear. 1982 May-Jun;3(3):135-47. doi: 10.1097/00003446-198205000-00007. No abstract available.
Results Reference
result
PubMed Identifier
12467367
Citation
Cox RM, Alexander GC. The International Outcome Inventory for Hearing Aids (IOI-HA): psychometric properties of the English version. Int J Audiol. 2002 Jan;41(1):30-5. doi: 10.3109/14992020209101309.
Results Reference
result
PubMed Identifier
9046067
Citation
Dillon H, James A, Ginis J. Client Oriented Scale of Improvement (COSI) and its relationship to several other measures of benefit and satisfaction provided by hearing aids. J Am Acad Audiol. 1997 Feb;8(1):27-43.
Results Reference
result
PubMed Identifier
7789669
Citation
Cox RM, Alexander GC. The abbreviated profile of hearing aid benefit. Ear Hear. 1995 Apr;16(2):176-86. doi: 10.1097/00003446-199504000-00005.
Results Reference
result
PubMed Identifier
24152691
Citation
Caballero FF, Miret M, Power M, Chatterji S, Tobiasz-Adamczyk B, Koskinen S, Leonardi M, Olaya B, Haro JM, Ayuso-Mateos JL. Validation of an instrument to evaluate quality of life in the aging population: WHOQOL-AGE. Health Qual Life Outcomes. 2013 Oct 23;11:177. doi: 10.1186/1477-7525-11-177.
Results Reference
result
Citation
Etymotic. QuickSIN Speech-in-Noise Test. Elk Grove Village, IL 2006.
Results Reference
result

Learn more about this trial

Improving Access and Affordability of Adult Hearing Healthcare

We'll reach out to this number within 24 hrs