Recent changes in attitudes of US adults toward people with epilepsy - Results from the 2005 SummerStyles and 2013 FallStyles surveys

被引:23
作者
Cui, Wanjun [1 ]
Kobau, Rosemarie [1 ]
Zack, Matthew M. [1 ]
Buelow, Janice M. [2 ]
Austin, Joan K. [3 ]
机构
[1] Ctr Dis Control & Prevent, Notional Ctr Chron Dis Prevent & Hlth Promot, Div Populat Hlth, Epilepsy Program, Atlanta, GA 30341 USA
[2] Epilepsy Fdn, Landover, MD 20785 USA
[3] Indiana Univ, Sch Nursing, Bloomington, IN 47408 USA
关键词
Stigma; Epilepsy; SummerStyles survey; FallStyles survey; US adults; Attitude and Beliefs about Living with Epilepsy (ABLE) scale; PUBLIC-ATTITUDES; UNITED-STATES; FELT STIGMA; HEALTH; POPULATION; CONFIDENCE; KNOWLEDGE; DISEASES; IMPACT;
D O I
10.1016/j.yebeh.2015.08.040
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Objectives: This study aimed to evaluate the validity and the reliability of two components of the Attitudes and Beliefs about Living with Epilepsy (ABLE) scale and to measure the magnitude of the public's attitudes and behaviors toward persons with epilepsy using U.S. nationally representative samples in 2005 and 2013. Methods: We used data fromthe cross-sectional 2005 SummerStyles and 2013 FallStyles surveys to test the underlying structure of 16 items of the work and role expectations and personal fear and social avoidance subscales of ABLE by performing exploratory factor analysis (EFA). We estimated the percentages and 95% confidence intervals of adults who agreed or disagreed with each item. We also calculated the mean score of each subscale and used linear regression to obtain means adjusted for selected sociodemographic characteristics. Results: Exploratory factor analysis confirmed a two-factor structure, but with the exception of omitting one item regarding work activities persons with epilepsy cannot do work activities safely, from one subscale. Both subscales also showed a high level of reliability (Cronbach's alpha = 0.8 and Cronbach's alpha = 0.9, respectively). Among the items in the work and role expectations subscale, a significantly higher percentage of adults in 2013 than in 2005 reported strongly or moderately agreeing that persons with epilepsy can do anything as well as anyone else (56.4%, 95% CI = 54.1-58.7 vs. 47.6%, 95% CI = 45.8-49.3) and can cope with everyday life (69.8%, 95% CI= 67.5-72.0 vs. 55.0%, 95% CI= 53.2-56.7). Among the items in the personal fear and social avoidance subscale, a significantly higher percentage of adults reported in 2013 than in 2005 strongly or moderately agreeing that they would be nervous around persons with epilepsy (25.4%, 95% CI = 23.4-27.5 vs. 16.8%, 95% CI = 15.4-18.2) and would avoid those with frequent seizures (12.4%, 95% CI = 11.0-13.9 vs. 7.6%, 95% CI = 6.7-8.7). The adjusted mean score for work and role expectations differed by sex, age, race/ethnicity, education, and income in both years. The adjusted mean score for personal fear and social avoidance differed by sex, age, race/ethnicity, education, and marital status. Negative attitudes were slightly but significantly higher in 2013 than in 2005. Conclusions: Centers for Disease Control and Prevention's ABLE scale is a valid and reliable scale that can be used to study and to track the public's attitudes and behaviors toward persons with epilepsy. Compared with 2005, US adults' reported level of expectations for personswith epilepsy improved only in certain aspects by 2013. Adults' level of personal fear and intention for social avoidance worsened from 2005 to 2013. Because the levels of expectations and of fear and social avoidance differed by sociodemographic characteristics, continued efforts tailored to specific groups are needed. To supplement educational programs focused on improving knowledge, new communication approaches grounded in decision theory that quell risk perceptions and allay negative emotional responses are recommended. Published by Elsevier Inc.
引用
收藏
页码:108 / 118
页数:11
相关论文
共 69 条
  • [41] Frequency of affective symptoms and their psychosocial impact in Korean people with epilepsy: A survey at two tertiary care hospitals
    Kwon, Oh-Young
    Park, Sung-Pa
    [J]. EPILEPSY & BEHAVIOR, 2013, 26 (01) : 51 - 56
  • [42] Lackey N.R., 2003, Making sense of factor analysis: The use of factor analysis for instrument development in health care research, DOI 10.4135/9781412984898
  • [43] Psychosocial and sociodemographic associates of felt stigma in epilepsy
    Leaffer, Emily B.
    Hesdorffer, Dale C.
    Begley, Charles
    [J]. EPILEPSY & BEHAVIOR, 2014, 37 : 104 - 109
  • [44] Emotion and Decision Making
    Lerner, Jennifer S.
    Li, Ye
    Valdesolo, Piercarlo
    Kassam, Karim S.
    [J]. ANNUAL REVIEW OF PSYCHOLOGY, VOL 66, 2015, 66 : 799 - 823
  • [45] Misinformation and Its Correction: Continued Influence and Successful Debiasing
    Lewandowsky, Stephan
    Ecker, Ullrich K. H.
    Seifert, Colleen M.
    Schwarz, Norbert
    Cook, John
    [J]. PSYCHOLOGICAL SCIENCE IN THE PUBLIC INTEREST, 2012, 13 (03) : 106 - 131
  • [46] Changes in public attitudes toward breastfeeding in the United States, 1999-2003
    Li, Ruowei
    Rock, Valerie J.
    Grummer-Strawn, Laurence
    [J]. JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 2007, 107 (01) : 122 - 127
  • [47] Lopez R., 2004, LATINOCOMMUNITYS CUL
  • [48] Past and present public knowledge and attitudes toward epilepsy in Italy
    Mecarelli, Oriano
    Capovilla, Giuseppe
    Romeo, Antonino
    Rubboli, Guido
    Tinuper, Paolo
    Beghi, Ettore
    [J]. EPILEPSY & BEHAVIOR, 2010, 18 (1-2) : 110 - 115
  • [49] Polychoric versus Pearson correlations in exploratory and confirmatory factor analysis of ordinal variables
    Pablo Holgado-Tello, Francisco
    Chacon-Moscoso, Salvador
    Barbero-Garcia, Isabel
    Vila-Abad, Enrique
    [J]. QUALITY & QUANTITY, 2010, 44 (01) : 153 - 166
  • [50] Epilepsy stigma and stigma by association in the workplace
    Parfene, Cristina
    Stewart, Tracie L.
    King, Tricia Z.
    [J]. EPILEPSY & BEHAVIOR, 2009, 15 (04) : 461 - 466