- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01940705
A Simplified Patient-Centered Educational Tool for Improved Hearing-Aid Outcomes
A Simplified Patient Centered Educational Tool for Improved Hearing Aid Outcomes
Study Overview
Status
Conditions
Detailed Description
Objectives: Reasons for non-use of hearing aids are varied, but many studies have suggested that a lack of knowledge about how to use and/or take care of the hearing aids is a major factor. This is not surprising given that other healthcare fields have reported that between 40-80% of information provided during a clinical appointment is forgotten by the patient immediately after the appointment and almost half of what is remembered is not correct. The long-term goal of this project is to improve the delivery of information during the hearing-aid orientation, as better delivery of information will result in better hearing-aid handling skills and thus better overall hearing-aid outcomes. To accomplish this goal, the investigators propose to refine and evaluate the effectiveness of three forms of supplemental hearing-aid-orientation tools, each of which was developed using established guidelines for good patient-provider communication.
Plan: The purpose of the proposed application is to evaluate the relative effectiveness of four forms of hearing-aid orientation provided to first time hearing-aid users, three of which use some of the aforementioned strategies to enhance the standard of care. The four forms of orientation will be: (1) the standard-of-care hearing-aid orientation; (2) the standard of care plus provision a hearing-aid information guide (HAIG) (3) the standard of care supplemented by an explanation of its content using the talk-back technique to confirm patient understanding; and (4) the standard of care plus provision of a take-home hearing-aid orientation DVD (HAO DVD). The content of the HAIG will be field tested and finalized following input obtained via focus groups with clinical audiologists and first-time hearing aid users.
Methods: For the field testing up to 16 clinical audiologists and 10 new hearing aid user Veterans will be recruited to participate in focus groups during which they will view and then be asked questions about the content of the HAIG. Information learned during these focus groups will then be incorporated into the HAIG, at which time they will be ready for use in the study. For the comparative effectiveness study, up to 468 hearing-impaired Veterans who are about to become first-time hearing-aid users will be enrolled to participate in this investigation. These individuals will be recruited from the VA Portland Health Care System's Audiology and Speech Pathology Service (ASPS). Prior to receiving their hearing aids, subjects will be enrolled in the study at the National Center for Rehabilitative Auditory Research (NCRAR), and will conduct health literacy, manual dexterity and hepatic sensitivity, visual acuity, and learning and memory assessments. They will then attend their hearing aid fitting in the ASPS and will receive standard-of-care hearing-aid orientation. At the end of that appointment, they will receive one of the four study interventions. Subjects will return to the NCRAR 4-6 weeks after the hearing-aid-fitting appointment to complete the following outcome measures: a knowledge and practical test regarding hearing-aid use and care, a measure of self-efficacy, and a measure of hearing-aid outcomes. They also will be interviewed so that the investigators can learn their opinions about the intervention. A subset of the initial 50 participants enrolled into each study arm will attend a second follow-up appointment 6 months after the fitting appointment so the investigators can examine longer-term impacts of the hearing aid orientation interventions.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Oregon
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Portland, Oregon, United States, 97239
- VA Portland Health Care System, Portland, OR
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Participants will be Veterans who are receiving hearing aids from the Audiology Clinic at the VA Portland Health Care System and who have had no prior experience using hearing aids. To be included in the study, participants will:
- Be approved and have plans to get bilateral hearing aid fitting at the VA Portland Health Care System .
- Be able to read and converse in English.
Exclusion Criteria:
- Be younger than 50 years or older than 89 years of age.
- Have a documented diagnosis of neurological, cognitive, visual, or other mental disorder, such as Alzheimer's disease, schizophrenia, current alcohol or substance abuse, as determined by chart review that would interfere with study completion.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Standard of care (SoC)
standard of care hearing-aid orientation as provided by clinical audiologist
|
standard of care hearing-aid orientation as provided by clinical audiologist
|
Experimental: SoC plus hearing-aid informational guide
standard of care hearing-aid orientation as provided by clinical audiologist plus a take-home informational guide regarding their hearing aids
|
standard of care hearing-aid orientation as provided by clinical audiologist
Printed take-home guide on hearing aids
|
Experimental: SoC plus hearing aid DVD
SoC hearing-aid orientation as provided by clinical audiologist plus a take-home hearing aid digital video disc
|
standard of care hearing-aid orientation as provided by clinical audiologist
Take-home DVD about hearing aids
|
Experimental: Soc plus teach-back technique
standard of care hearing-aid orientation as provided by clinical audiologist plus a teach-back technique session reviewing information on the hearing aids
|
standard of care hearing-aid orientation as provided by clinical audiologist
Counseling/Educational session using the teach-back technique to review information about their hearing aids
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hearing Aid Skills and Knowledge Test
Time Frame: 4 weeks after the hearing-aid fitting
|
Hearing Aid Skills and Knowledge measures knowledge and skills for tasks associated with hearing aid management, such as knowledge of and ability to change batteries, insert the hearing aid, etc. For knowledge scale, participant gives a verbal response. Items are assigned points: 0 (incorrect response) or 1 (correct response). For skills scale, participant conducts the required task. Items are assigned points: 0 (Could not perform task), 1 (Achieved with some difficulty, more than one attempt) or 2 (Achieved with no difficulty on first attempt). There were 15 knowledge items and 19 skill items. Percent correct was computed for each scale separately. Points were totaled, divided by the no. items with valid data, and multiplied by 100, with a correction to equate subscales. For the skills scale, percent correct scores were calculated based upon the notion that a value of 2 was considered 100% correct, 1 was considered 50% correct. |
4 weeks after the hearing-aid fitting
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Measure of Audiologic Rehabilitation Self-Efficacy for Hearing Aids
Time Frame: 4 weeks after the hearing-aid fitting
|
12-item questionnaire assessing self-efficacy for basic and advanced hearing aid handling skills.
Item responses are on a scale of 0 to 100 in 10 point increments.
Score of 0 = no self efficacy to100 = complete self efficacy.
Final score is an average of individual item responses.
|
4 weeks after the hearing-aid fitting
|
International Outcome Inventory for Hearing Aids.
Time Frame: 4 weeks after the hearing-aid fitting
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Hearing-aid outcomes questionnaire assessing benefit, satisfaction, use, etc.
Seven items, each on a scale of 1-5. 1 = low satisfaction/benefit/use etc., 5 = maximum satisfaction/benefit/use etc.
A total score is derived by summing the score from each of the seven items.
Total scores range from a low of 7 to a high of 35.
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4 weeks after the hearing-aid fitting
|
Collaborators and Investigators
Investigators
- Principal Investigator: M. Samantha Lewis, PhD, VA Portland Health Care System, Portland, OR
- Principal Investigator: Gabrielle H Saunders, VA Portland Health Care System, Portland, OR
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- C1260-R
- 1I01RX001260-01 (U.S. NIH Grant/Contract)
- 3224 (Portland VA IRB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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