Epilepsy and well-being
This study examined the association between social, psychological and physical well-being and a range of epilepsy-related and socio-demographic variables in a sample of people with epilepsy. A questionnaire method was used and the sample of 392 people with epilepsy was drawn from urban and rural epi...
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Veröffentlicht in: | Social science & medicine (1982) 1990, Vol.31 (2), p.165-170 |
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container_title | Social science & medicine (1982) |
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creator | Collings, John A. |
description | This study examined the association between social, psychological and physical well-being and a range of epilepsy-related and socio-demographic variables in a sample of people with epilepsy. A questionnaire method was used and the sample of 392 people with epilepsy was drawn from urban and rural epilepsy support groups in several regions of Great Britain and Ireland, and a hospital out-patients' population. The findings revealed that people's perceptions of themselves and of their epilepsy were the variables most strongly related to overall well-being, and that seizure frequency, time since diagnosis, a diagnosis of absence seizures and being employed full-time also seemed of some importance. The study's findings have implications for the management of people with epilepsy and suggest that ratings of subjective experience could be usefully incorporated into future research on social and psychological aspects of seizure disorders and other disabilities. |
doi_str_mv | 10.1016/0277-9536(90)90058-Z |
format | Article |
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A questionnaire method was used and the sample of 392 people with epilepsy was drawn from urban and rural epilepsy support groups in several regions of Great Britain and Ireland, and a hospital out-patients' population. The findings revealed that people's perceptions of themselves and of their epilepsy were the variables most strongly related to overall well-being, and that seizure frequency, time since diagnosis, a diagnosis of absence seizures and being employed full-time also seemed of some importance. The study's findings have implications for the management of people with epilepsy and suggest that ratings of subjective experience could be usefully incorporated into future research on social and psychological aspects of seizure disorders and other disabilities.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Data Collection</subject><subject>Epilepsy</subject><subject>Epilepsy - epidemiology</subject><subject>Epilepsy - psychology</subject><subject>epilepsy well-being psychosocial quality of life</subject><subject>Female</subject><subject>Great Britain</subject><subject>Humans</subject><subject>Ireland</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>psychosocial</subject><subject>Psychosocial Factors</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Quality of Life</subject><subject>Self Concept</subject><subject>Self image</subject><subject>Sociodemographic Factors</subject><subject>United Kingdom</subject><subject>Well Being</subject><issn>0277-9536</issn><issn>1873-5347</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>X2L</sourceid><sourceid>BHHNA</sourceid><recordid>eNqFkb1vFDEQxS1EFI5AnQakCEUoFEtm_LlukKIoJEGRaEiTxvJ5Z4Ojvd2NfZfo_nu83HEFBRRjS57fe5p5ZuwdwmcE1KfAjamsEvrEwicLoOrq7gWbYW1EpYQ0L9lsh7xir3N-AACEWuyzfS5qi4rP2OHFGDsa8_rI983RM3VdNafY379he63vMr3d3gfs9uvFj_Or6ub75fX52U0VFOKy0lI1c95YULydWx6MAEMYENFYCdz7OrQBW4MKW0_cI5dKg9QEurUmeHHAPm58xzQ8rigv3SLmUMbwPQ2r7Iy1yhhp_gtq5NpKbQv44S_wYVilvizhuACppBWTm9xAIQ05J2rdmOLCp7VDcFO6borOTdE5C-53uu6uyL5tZIlGCjsNEeUhLKhxT054geVYl0JbpMLHUrzUOD1p5dCA-7lcFLP320FX80n7x237N6V_vO37HHzXJt-HmHeY1KgEiIJ92WBUvukpUnI5ROoDNTFRWLpmiP9e6hdt4qsJ</recordid><startdate>1990</startdate><enddate>1990</enddate><creator>Collings, John A.</creator><general>Elsevier Ltd</general><general>Elsevier</general><general>Pergamon Press Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>DKI</scope><scope>X2L</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U3</scope><scope>7U4</scope><scope>8BJ</scope><scope>BHHNA</scope><scope>DWI</scope><scope>FQK</scope><scope>JBE</scope><scope>K9.</scope><scope>WZK</scope><scope>7X8</scope></search><sort><creationdate>1990</creationdate><title>Epilepsy and well-being</title><author>Collings, John A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-645db2d9052fb92c7307e1c11179402aa8cfc1f7151fae2a12456046e06f97ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Data Collection</topic><topic>Epilepsy</topic><topic>Epilepsy - epidemiology</topic><topic>Epilepsy - psychology</topic><topic>epilepsy well-being psychosocial quality of life</topic><topic>Female</topic><topic>Great Britain</topic><topic>Humans</topic><topic>Ireland</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>psychosocial</topic><topic>Psychosocial Factors</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Quality of Life</topic><topic>Self Concept</topic><topic>Self image</topic><topic>Sociodemographic Factors</topic><topic>United Kingdom</topic><topic>Well Being</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Collings, John A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>RePEc IDEAS</collection><collection>RePEc</collection><collection>CrossRef</collection><collection>Social Services Abstracts</collection><collection>Sociological Abstracts (pre-2017)</collection><collection>International Bibliography of the Social Sciences (IBSS)</collection><collection>Sociological Abstracts</collection><collection>Sociological Abstracts</collection><collection>International Bibliography of the Social Sciences</collection><collection>International Bibliography of the Social Sciences</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Sociological Abstracts (Ovid)</collection><collection>MEDLINE - Academic</collection><jtitle>Social science & medicine (1982)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Collings, John A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epilepsy and well-being</atitle><jtitle>Social science & medicine (1982)</jtitle><addtitle>Soc Sci Med</addtitle><date>1990</date><risdate>1990</risdate><volume>31</volume><issue>2</issue><spage>165</spage><epage>170</epage><pages>165-170</pages><issn>0277-9536</issn><eissn>1873-5347</eissn><coden>SSMDEP</coden><abstract>This study examined the association between social, psychological and physical well-being and a range of epilepsy-related and socio-demographic variables in a sample of people with epilepsy. A questionnaire method was used and the sample of 392 people with epilepsy was drawn from urban and rural epilepsy support groups in several regions of Great Britain and Ireland, and a hospital out-patients' population. The findings revealed that people's perceptions of themselves and of their epilepsy were the variables most strongly related to overall well-being, and that seizure frequency, time since diagnosis, a diagnosis of absence seizures and being employed full-time also seemed of some importance. The study's findings have implications for the management of people with epilepsy and suggest that ratings of subjective experience could be usefully incorporated into future research on social and psychological aspects of seizure disorders and other disabilities.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>2389152</pmid><doi>10.1016/0277-9536(90)90058-Z</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Data Collection Epilepsy Epilepsy - epidemiology Epilepsy - psychology epilepsy well-being psychosocial quality of life Female Great Britain Humans Ireland Male Medical research Medical sciences Middle Aged psychosocial Psychosocial Factors Public health. Hygiene Public health. Hygiene-occupational medicine Quality of Life Self Concept Self image Sociodemographic Factors United Kingdom Well Being |
title | Epilepsy and well-being |
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