A Survey of Selected Representations of the Stroke and Aphasia Quality of Life Scale-39 Items PDF Download
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Author: Dara Lynn Elizabeth Deroche
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Languages : en
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Author: Dara Lynn Elizabeth Deroche
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Languages : en
Pages :
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Author: Taylor Ashton Glorioso
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Languages : en
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Author: Lea J. Heise-Jensen
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Category :
Languages : en
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Author: Samantha Marie Studrawa
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Category :
Languages : en
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Category : Aphasic persons
Languages : en
Pages :
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Author: Panagiotis Vlamos
Publisher: Springer Nature
ISBN: 3031319869
Category : Medical
Languages : en
Pages : 665
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The 5th World Congress on Genetics, Geriatrics, and Neurodegenerative Diseases Research (GeNeDis 2022) focuses on the latest major challenges in scientific research, new drug targets, the development of novel biomarkers, new imaging techniques, novel protocols for early diagnosis of neurodegenerative diseases, and several other scientific advances, with the aim of better, safer, and healthier aging. This volume focuses on the sessions from the conference on Neuroscientific Advances.
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Languages : en
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Author: Leah Marie Ryan
Publisher:
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Category : Electronic dissertations
Languages : en
Pages : 72
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The purpose of this study was to compare two quality of life measures designed for persons with aphasia. Five persons with chronic expressive aphasia and their nominated family member/caregiver participated in this study. A preliminary interview was conducted with each participant. The Stroke and Aphasia Quality of Life Scale (SAQOL-39) and Assessment for Living with Aphasia (ALA) were then administered. Assessments were administered to family members under two conditions: (1) how they would rate the PWA’s quality of life and (2) how they thought the PWA would rate themselves. A brief post-assessment interview was then given to help establish the validity of the quality of life assessments given. The reported outcomes on individual measures for each participant were compared against outcomes on the other (i.e., SAQOL-39 vs. ALA). Outcomes reported by the PWA were then compared to those reported by their family member. Responses from the preliminary interviews were analyzed to establish common themes, as well as to aid in establishing validity of the quality of life assessments used. Results indicated substantial variances existed between assessment outcomes and PWAs vs. family members. The dual presentation (i.e., “as” PWA and “for” PWA) of each assessment allowed responses by caregivers to be closer to those of the PWA, suggesting that similar practice or at minimum a “priming” of the caregiver should occur prior to administration of any qualitative assessment for which they will serve as proxy to gain the most accurate picture. Outcomes also suggested that these assessments, in combination best captured the overall picture for each PWA’s quality of life.
Author: Linda Worrall
Publisher: Psychology Press
ISBN: 9781841699462
Category : Medical
Languages : en
Pages : 92
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This special issue of the journal Aphasiologyis dedicated to the topic of quality of life in aphasia.
Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309489385
Category : Medical
Languages : en
Pages : 445
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The U.S. Social Security Administration (SSA) provides disability benefits through the Social Security Disability Insurance (SSDI) and Supplemental Security Income (SSI) programs. To receive SSDI or SSI disability benefits, an individual must meet the statutory definition of disability, which is "the inability to engage in any substantial gainful activity [SGA] by reason of any medically determinable physical or mental impairment which can be expected to result in death or which has lasted or can be expected to last for a continuous period of not less than 12 months." SSA uses a five-step sequential process to determine whether an adult applicant meets this definition. Functional Assessment for Adults with Disabilities examines ways to collect information about an individual's physical and mental (cognitive and noncognitive) functional abilities relevant to work requirements. This report discusses the types of information that support findings of limitations in functional abilities relevant to work requirements, and provides findings and conclusions regarding the collection of information and assessment of functional abilities relevant to work requirements.
