- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01809496
Hearing Aids, Counseling and the Significant Other
Auditory Rehabilitation From the Perspective of the Significant Other
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Oregon
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Portland, Oregon, United States, 97207
- Portland VA Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria: Both men and women with hearing loss and their live-in partners will serve as subjects in this study. The subjects with hearing loss will have a mild to moderately-severe hearing loss in both of the ears, will have word recognition scores of 40% or better bilaterally, and will be about to get new hearing aids. Live-in partners may also have up to a moderately-severe degree of hearing loss but cannot have prior experience with hearing aids nor have plans to get hearing aids during the course of their participation in this study. Their word recognition scores should also be 40% or better bilaterally. All subjects also will meet the following additional inclusion criteria:
- Age 20-85 years;
- Intact mental status as assessed by the Mini-Mental State Examination (MMSE; Folstein, Folstein & McHugh, 1975);
- No evidence of any major medical illness requiring long-term assistive care, as determined by the Katz Index of Independence in Activities of Daily Living (Katz, Down, Cash &Grotz, 1970);
- Able to read and respond to English; and
- Willing and able to give written informed consent to participate in this investigation.
Exclusion Criteria: Failure to satisfy any of the requirements listed above or if their live-in partner fails to meet the criteria.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Active Comparator: Informational counseling, patient only
The purpose of this experimental group is to evaluate the effectiveness of informational counseling alone.
This type of counseling is considered the standard of care in audiologic practice.
Patients in this will review this material in detail with a member of the study team for approximately 30 minutes at the second visit.
Spouses in this experimental group will be will review material regarding VA services with a member of the study team for about 30 minutes.
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Experimental: Informational Counseling, couples
The purpose of this experimental group is to evaluate the influence of spousal involvement when receiving informational counseling.
In this manner, both patients and spouses are presented with the same information regarding hearing loss and hearing aids.
Couples in this experimental group will be given the same information that the patients in the first group were given.
At the second visit, couples in this group will review this information together with a member of the research team for approximately 30 minutes.
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Experimental: Patient Centered Counseling,patient only
In order to assess the effects of enhanced patient-centered counseling (PCC), the patients assigned to this group will meet together with either Dr. Lewis or the Research Audiologist for approximately 30 minutes of counseling.
In addition to the PCC techniques used in audiology, this counseling also will involve the core components of motivational interviewing.
These principles and methods will be used to allow the patient to clearly express his/her expectations of, concerns about, and motivations for hearing-aid use.
The spouses in this experimental group will be given information regarding VA services.
This material will be reviewed with a member of the research team for about 30 minutes at the second visit.
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Other Names:
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Experimental: Patient Centered Counseling, couples
In order to assess the influence of the spouse on the enhanced PCC process, the couples assigned to this group will meet together with either Dr. Lewis or the Research Audiologist for approximately 30 minutes of counseling.
This counseling will be conducted with both the patient and the spouse together, giving both partners time to express their thoughts.
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Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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post-use subjective opinions regarding the hearing aids
Time Frame: 4-6 weeks after the hearing aid fitting
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questionnaires
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4-6 weeks after the hearing aid fitting
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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pre-use hearing aid expectations
Time Frame: immediately after the intervention at Visit #2 (Day 0)
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questionnaire
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immediately after the intervention at Visit #2 (Day 0)
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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self-efficacy
Time Frame: 4-6 weeks after the hearing aid fitting
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questionnaires
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4-6 weeks after the hearing aid fitting
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hearing aid use
Time Frame: 4-6 weeks after the hearing aid fitting
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datalogging
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4-6 weeks after the hearing aid fitting
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: M. Samantha Lewis, PhD, VA National Center for Rehabilitative Auditory Research
Publications and helpful links
General Publications
- Folstein MF, Folstein SE, McHugh PR. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975 Nov;12(3):189-98. doi: 10.1016/0022-3956(75)90026-6. No abstract available.
- Katz S, Downs TD, Cash HR, Grotz RC. Progress in development of the index of ADL. Gerontologist. 1970 Spring;10(1):20-30. doi: 10.1093/geront/10.1_part_1.20. No abstract available.
Study record dates
Study Major Dates
Study Start
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- C7067W
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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