Literature DB >> 24866252

A model for internalized stigma in children and adolescents with epilepsy.

Joan K Austin1, Susan M Perkins2, David W Dunn3.   

Abstract

OBJECTIVE: Perceptions of stigma in children and adolescents with epilepsy are associated with higher rates of mental health problems. The purpose of this study was to test relationships in a model that identified variables most strongly associated with perceptions of stigma in children and adolescents with epilepsy. Our ultimate goal is to develop a theoretical foundation for future intervention research by identifying variables associated with perceptions of stigma that are potentially amenable to psychosocial interventions.
METHODS: Participants were 173 children and adolescents with epilepsy who were between 9 and 14 years of age. Data were collected in telephone interviews. Stigma was measured using a self-report scale. Data were analyzed using structural equation modeling.
RESULTS: Greater need for information and support, more fear and worry related to having epilepsy, greater seizure severity, and younger age were significantly associated with greater perceptions of stigma. Female gender, greater need for information and support, having at least one seizure in the past year, and lower self-efficacy for seizure management were significantly associated with more fear and worry related to having epilepsy.
CONCLUSIONS: Findings suggest that perceptions of stigma are associated with two variables that are amenable to psychosocial interventions: fear and worry about having epilepsy and need for information and support. Future research should test the efficacy of interventions that reduce fear and worry, provide information about epilepsy, and reduce need for support.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Children and adolescents; Emotional support needs; Epilepsy; Information needs; Stigma

Mesh:

Year:  2014        PMID: 24866252      PMCID: PMC4096577          DOI: 10.1016/j.yebeh.2014.04.020

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  23 in total

1.  Stigma interventions and research for international health.

Authors:  Mitchell G Weiss; Jayashree Ramakrishna
Journal:  Lancet       Date:  2006-02-11       Impact factor: 79.321

2.  The development of a seizure severity scale as an outcome measure in epilepsy.

Authors:  G A Baker; D F Smith; M Dewey; J Morrow; P M Crawford; D W Chadwick
Journal:  Epilepsy Res       Date:  1991-04       Impact factor: 3.045

3.  Brief report: Adolescents' attitudes toward epilepsy: further validation of the Child Attitude Toward Illness Scale (CATIS).

Authors:  T E Heimlich; L E Westbrook; J K Austin; J A Cramer; O Devinsky
Journal:  J Pediatr Psychol       Date:  2000 Jul-Aug

Review 4.  Interventions to reduce epilepsy-associated stigma.

Authors:  G Birbeck
Journal:  Psychol Health Med       Date:  2006-08       Impact factor: 2.423

5.  Epilepsy familiarity, knowledge, and perceptions of stigma: report from a survey of adolescents in the general population.

Authors:  Joan K. Austin; Patricia Osborne Shafer; Jessica Beach Deering
Journal:  Epilepsy Behav       Date:  2002-08       Impact factor: 2.937

6.  Youth With Epilepsy: Development of a Model of Children's Attitudes Toward Their Condition.

Authors:  Joan K Austin; David W Dunn; Susan M Perkins; Jianzhao Shen
Journal:  Child Health Care       Date:  2006

7.  Continuing psychosocial care needs in children with new-onset epilepsy and their parents.

Authors:  Cheryl P Shore; Janice M Buelow; Joan K Austin; Cynthia S Johnson
Journal:  J Neurosci Nurs       Date:  2009-10       Impact factor: 1.230

8.  Behavioral issues involving children and adolescents with epilepsy and the impact of their families: recent research data.

Authors:  Joan K Austin; David W Dunn; Cynthia S Johnson; Susan M Perkins
Journal:  Epilepsy Behav       Date:  2004-10       Impact factor: 2.937

9.  Psychosocial factors associated with stigma in adults with epilepsy.

Authors:  Gigi Smith; Pamela L Ferguson; Lee L Saunders; Janelle L Wagner; Braxton B Wannamaker; Anbesaw W Selassie
Journal:  Epilepsy Behav       Date:  2009-09-24       Impact factor: 2.937

10.  Development of scales to measure psychosocial care needs of children with seizures and their parents. 1.

Authors:  J Austin; D Dunn; G Huster; D Rose
Journal:  J Neurosci Nurs       Date:  1998-06       Impact factor: 1.230

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Review 5.  Quality of Life and Stigma in Epilepsy, Perspectives from Selected Regions of Asia and Sub-Saharan Africa.

Authors:  Warren Boling; Margaret Means; Anita Fletcher
Journal:  Brain Sci       Date:  2018-04-01

6.  Why do children and adolescents with epilepsy disclose or not disclose their condition to their friends?

Authors:  Sarah Jeschke; Sarah Woltermann; Martina Patrizia Neininger; Josefine Pauschek; Wieland Kiess; Thilo Bertsche; Astrid Bertsche
Journal:  Eur J Pediatr       Date:  2020-05-05       Impact factor: 3.183

  6 in total

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