Literature DB >> 20921880

Development and validity of the Family Stigma in Alzheimer's disease Scale (FS-ADS).

Perla Werner1, Dovrat Goldstein, Jeremia Heinik.   

Abstract

Although it is widely assumed that persons with Alzheimer disease (AD) and their family caregivers are victims of stigmatization, family stigma in the area of AD has received surprisingly limited attention. Reliable, valid, and user-friendly scales are a first step in expanding this body of knowledge. The aim of this study was to develop and examine the validity of the Family Stigma in Alzheimer's disease Scale. Interviews were conducted with 185 children of persons with AD. A pool of 100 items was identified from the literature and an earlier qualitative study including 3 dimensions (caregivers' stigma, lay persons' stigma, and structural stigma). Exploratory factor analyses, theoretical relevance, and internal reliability analyses allowed us to reduce the pull to 62 items. Regarding construct validity, statistically significant associations were found between family stigma and caregivers' burden and behavioral problems, in most of the scales. Although further testing is warranted, these findings indicate that the Family Stigma in Alzheimer's disease Scale is a reliable and valid instrument for assessing stigma in the context of AD.
Copyright © 2011 by Lippincott Williams & Wilkins

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Year:  2011        PMID: 20921880     DOI: 10.1097/WAD.0b013e3181f32594

Source DB:  PubMed          Journal:  Alzheimer Dis Assoc Disord        ISSN: 0893-0341            Impact factor:   2.703


  13 in total

1.  The effect of disease risk probability and disease type on interest in clinic-based versus direct-to-consumer genetic testing services.

Authors:  Kerry Sherman; Laura-Kate Shaw; Katrina Champion; Fernanda Caldeira; Margaret McCaskill
Journal:  J Behav Med       Date:  2015-03-27

2.  Identifiable Characteristics and Potentially Malleable Beliefs Predict Stigmatizing Attributions Toward Persons With Alzheimer's Disease Dementia: Results of a Survey of the U.S. General Public.

Authors:  Shana D Stites; Rebecca Johnson; Kristin Harkins; Pamela Sankar; Dawei Xie; Jason Karlawish
Journal:  Health Commun       Date:  2016-12-29

3.  The relative contributions of biomarkers, disease modifying treatment, and dementia severity to Alzheimer's stigma: A vignette-based experiment.

Authors:  Shana D Stites; Jeanine Gill; Emily A Largent; Kristin Harkins; Pamela Sankar; Abba Krieger; Jason Karlawish
Journal:  Soc Sci Med       Date:  2021-12-01       Impact factor: 4.634

4.  Levels and correlates of knowledge about Alzheimer's disease among older Chinese Americans.

Authors:  Fei Sun; Xiang Gao; Hui Shen; Denise Burnette
Journal:  J Cross Cult Gerontol       Date:  2014-06

5.  What features of stigma do the public most commonly attribute to Alzheimer's disease dementia? Results of a survey of the U.S. general public.

Authors:  Shana D Stites; Jonathan D Rubright; Jason Karlawish
Journal:  Alzheimers Dement       Date:  2018-03-27       Impact factor: 21.566

6.  Asian Americans' concerns and plans about Alzheimer's disease: The role of exposure, literacy and cultural beliefs.

Authors:  Yuri Jang; Hyunwoo Yoon; Nan Sook Park; Min-Kyoung Rhee; David A Chiriboga
Journal:  Health Soc Care Community       Date:  2017-10-04

7.  Effects of Self-Identification as a Caregiver on Expectations of Public Stigma of Alzheimer's Disease.

Authors:  Shana D Stites; Emily A Largent; Rebecca Johnson; Kristin Harkins; Jason Karlawish
Journal:  J Alzheimers Dis Rep       Date:  2021-01-16

8.  Using the Affiliate Stigma Scale with caregivers of people with dementia: psychometric evaluation.

Authors:  Chih-Cheng Chang; Jian-An Su; Chung-Ying Lin
Journal:  Alzheimers Res Ther       Date:  2016-10-26       Impact factor: 6.982

Review 9.  Advances in Alzheimer's imaging are changing the experience of Alzheimer's disease.

Authors:  Shana D Stites; Richard Milne; Jason Karlawish
Journal:  Alzheimers Dement (Amst)       Date:  2018-03-19

10.  Caregiver Stigma and Burden in Memory Disorders: An Evaluation of the Effects of Caregiver Type and Gender.

Authors:  Phoebe V Kahn; Heather A Wishart; Jennifer S Randolph; Robert B Santulli
Journal:  Curr Gerontol Geriatr Res       Date:  2016-01-28
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