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The Social and Cultural Context of Coping with Sickle Cell Disease

III. Stress, Coping Tasks, Family Functioning, and Children's Adjustment

Datos Bibliográficos

ID2344073
AutoresO A Barbarin (0000-0003-3075-2986, University of Michigan), Charles F Whitten (Wayne State University Medical School), Sandy Bond (Comprehensive Sickle Cell Clinic, Children’s Hospital of Michigan), Rhonda Conner-Warren (Comprehensive Sickle Cell Clinic, Children’s Hospital of Michigan), Rhonda Conner‐warren (Children's Hospital of Michigan)
Año1999
Volumen25
Número3
Páginas356-377
Fecha de publicación1999-08-01
Open AccessSí
TipoARTICLE
RevistaJournal of Black Psychology (JOURNAL)
Identificadores de la revistaISSN: 0095-7984 • E-ISSN: 1552-4558
EditorialSAGE Publications Inc (PUBLISHER)
DOI10.1177/0095798499025003006
OpenAlexW2106049152
IdiomaEN
Citas recibidas4
Referencias citadas18

Conceptions of individual and family coping with sickle cell disease (SCD) must incorporate several disease and sociocultural factors. This article proposes an integrative model and tests the relative contribution of model parameters to the prediction of social, academic, and psychological adjustment of children with SCD. The individual coping and family functioning variables most highly predictive of the child's psychological outcomes (anxiety, depression, and positive mood) include parental psychological functioning, maturity demands made of the ill child, and the quality of relations with parents and siblings. Academic adjustment was significantly predicted by parental academic expectations and by the child's rejection of a restrictive sick role. Competent social functioning also was predicted by the extent to which the ill child rejected the role of being sick

Anxiety · Coping (psychology · Developmental psychology · Disease · Mood · Psychiatry · Social environment · Social support · Clinical Psychology · Hemoglobinopathies and Related Disorders · Medicine · Psychology · Religion, Society, and Development · Religion, Spirituality, and Psychology · Social Psychology

  • The Lived Experiences of Caregivers of Children with Sickle Cell Disease

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    Open Access•Elizabeth Davenport Pollock, Josh B Kazman et al.•Journal of Black Psychology•2015

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    Open Access•H J Eysenck•Behaviour Research and Therapy•1985

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    Open Access•O A Barbarin•Journal of Community Psychology•1983

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  • Do Parental Coping, Involvement, Religiosity, and Racial Identity Mediate Children's Psychological Adjustment to Sickle Cell Disease

    Open Access•O A Barbarin•Journal of Black Psychology•1999

  • The Social and Cultural Context of Coping with Sickle Cell Disease

    Open Access•O A Barbarin, Charles F Whitten et al.•Journal of Black Psychology•1999

Citas por año0,21
Intervalo de citas2007 - 2022 (16)
Altamente citadoNo
Abrir DOISci-HubOpen Access
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