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Screening for Auditory Impairment — Which Hearing Assessment Test (SAI-WHAT): RCT design and baseline characteristics

Abstract Background Effective screening programs should not merely detect presence of disease, but also lead to long-term benefit. We describe the rationale and design of the first randomized clinical trial to study the long-term effects of routine screening for hearing loss. We also describe the ba...

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Published in:Contemporary clinical trials 2007-05, Vol.28 (3), p.303-315
Main Authors: Yueh, Bevan, Collins, Margaret P, Souza, Pamela E, Heagerty, Patrick J, Liu, Chuan-Fen, Boyko, Edward J, Loovis, Carl F, Fausti, Stephen A, Hedrick, Susan C
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container_start_page 303
container_title Contemporary clinical trials
container_volume 28
creator Yueh, Bevan
Collins, Margaret P
Souza, Pamela E
Heagerty, Patrick J
Liu, Chuan-Fen
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Hedrick, Susan C
description Abstract Background Effective screening programs should not merely detect presence of disease, but also lead to long-term benefit. We describe the rationale and design of the first randomized clinical trial to study the long-term effects of routine screening for hearing loss. We also describe the baseline characteristics of the randomized cohort. Methods We randomized 2305 veterans age 50 years or older to a control arm without screening, or to screening with: physiologic testing (AudioScope), a self-administered questionnaire (Hearing Handicap Inventory for the Elderly-Screening version [HHIE-S]), or both tests. The primary outcome measure will be hearing aid use one year after screening. We will also study a number of secondary outcomes, including appointments made with and visits to an audiologist, cases of aidable hearing loss, hearing aids dispensed, self-rated communication ability, and hearing-related quality of life. Results Baseline demographic and health status measures were evenly distributed across the screening arms. The percentage of patients who screened positive for hearing loss was 18.6%, 59.2%, and 63.6% for the AudioScope, HHIE-S, and combined screening arms, respectively. Implications Long-term results are needed to gain insight into whether the AudioScope is associated with high rates of false negative screening, the HHIE-S is associated with high rates of false positive screening, or a combination of both. Identifying the best screening program will depend on determining which strategy leads to successful hearing aid use.
doi_str_mv 10.1016/j.cct.2006.08.008
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We describe the rationale and design of the first randomized clinical trial to study the long-term effects of routine screening for hearing loss. We also describe the baseline characteristics of the randomized cohort. Methods We randomized 2305 veterans age 50 years or older to a control arm without screening, or to screening with: physiologic testing (AudioScope), a self-administered questionnaire (Hearing Handicap Inventory for the Elderly-Screening version [HHIE-S]), or both tests. The primary outcome measure will be hearing aid use one year after screening. We will also study a number of secondary outcomes, including appointments made with and visits to an audiologist, cases of aidable hearing loss, hearing aids dispensed, self-rated communication ability, and hearing-related quality of life. Results Baseline demographic and health status measures were evenly distributed across the screening arms. The percentage of patients who screened positive for hearing loss was 18.6%, 59.2%, and 63.6% for the AudioScope, HHIE-S, and combined screening arms, respectively. Implications Long-term results are needed to gain insight into whether the AudioScope is associated with high rates of false negative screening, the HHIE-S is associated with high rates of false positive screening, or a combination of both. 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The percentage of patients who screened positive for hearing loss was 18.6%, 59.2%, and 63.6% for the AudioScope, HHIE-S, and combined screening arms, respectively. Implications Long-term results are needed to gain insight into whether the AudioScope is associated with high rates of false negative screening, the HHIE-S is associated with high rates of false positive screening, or a combination of both. 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The percentage of patients who screened positive for hearing loss was 18.6%, 59.2%, and 63.6% for the AudioScope, HHIE-S, and combined screening arms, respectively. Implications Long-term results are needed to gain insight into whether the AudioScope is associated with high rates of false negative screening, the HHIE-S is associated with high rates of false positive screening, or a combination of both. Identifying the best screening program will depend on determining which strategy leads to successful hearing aid use.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17030153</pmid><doi>10.1016/j.cct.2006.08.008</doi><tpages>13</tpages></addata></record>
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subjects Adult and adolescent clinical studies
Biological and medical sciences
Cardiovascular
Depression
Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology
Female
Follow-Up Studies
Hearing Aids
Hearing loss
Hearing Loss - diagnosis
Hearing Loss - therapy
Hematology, Oncology and Palliative Medicine
Humans
Male
Mass Screening - methods
Medical sciences
Middle Aged
Mood disorders
Non tumoral diseases
Otorhinolaryngology. Stomatology
Patient compliance
Patient outcome assessment
Patient Selection
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Quality of life
Randomized controlled trials
Rehabilitation of hearing impaired
Research Design
Screening
Surveys and Questionnaires
Treatment effectiveness
Veterans
Washington
title Screening for Auditory Impairment — Which Hearing Assessment Test (SAI-WHAT): RCT design and baseline characteristics
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