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Quality in services for disabled children and their families

What Can Theory, Policy and Research on Children's and Parents' Views Tell Us

Datos Bibliográficos

ID5810491
AutoresWendy Mitchell (0000-0003-0862-7935, University of York), Patricia Sloper (University of York)
Año2001
Volumen15
Número4
Páginas237-252
Fecha de publicación2001-09-01
Peer ReviewedSí
Open AccessSí
TipoARTICLE
RevistaChildren & Society (JOURNAL)
Identificadores de la revistaISSN: 0951-0605 • E-ISSN: 1099-0860
EditorialWiley (PUBLISHER • GB)
DOI10.1002/chi.658
OpenAlexW2102430687
IdiomaEN
Citas recibidas17
Referencias citadas10

Many discourses surround the concept of 'service quality', however, it continues to remain partial and ambiguous. This paper seeks to unpack 'quality' in services for disabled children and their families. Theoretical models are initially reviewed and then considered in relation to key policy guidelines, empirical data drawing upon parents' and children's experiences of 'quality' in services are presented. This paper demonstrates the many different levels within the concept of 'quality' and highlights the importance of recognising and respecting that children and parents frequently value different aspects of 'quality'. Copyright (c) 2001 John Wiley & Sons, Ltd

Empirical research · Value (mathematics · Family and Disability Support Research · Geriatric Care and Nursing Homes · Healthcare innovation and challenges

  • Quality Indicators

    Wendy Mitchell•The British Journal of Social Work•2003

  • Approaches that Address Social Inclusion for Children with Disabilities

    Open Access•Donna Koller, Kevin P Stoddart et al.•Child & Youth Care Forum•2021

  • Access and achievement or social exclusion?’ are the government's policies working for disabled children and their families

    Open Access•Philippa Russell•Children & Society•2003

  • Tactics and Strategies of Family Adaptation among Parents Caring for Children and Youth with Developmental Disabilities

    Open Access•Elise J Matthews, Vivian Puplampu et al.•Global Qualitative Nursing Research•2021

  • Short Break and Respite Services for Disabled Children in England

    Open Access•Vicki Welch, Michelle Collins et al.•Children & Society•2014

  • Doing research with children and young people who do not use speech for communication

    Open Access•Parvaneh Rabiee, Patricia Sloper et al.•Children & Society•2005

  • The Quality‐Defining Process in Early Years Services

    Open Access•Emily C Tanner, Emily Tanner et al.•Children & Society•2006

  • Participation of disabled children in individual decisions about their lives and in public decisions about service development

    Open Access•Judith Cavet, Patricia Sloper•Children & Society•2004

  • Human dignity at stake – how parents of disabled children experience the welfare system

    Open Access•Tonje Gundersen•Scandinavian Journal of…•2011

  • Participation and partnerships in research

    S J Lister, Steve Lister et al.•International Journal of Social…•2003

  • I Value What You have to Say'. Seeking the Perspective of Children with a Disability, Not Just their Parents

    Belinda Garth, Rosalie Aroni•Disability & Society•2003

  • Desired outcomes for children and young people with complex health care needs, and children who do not use speech for communication

    Open Access•Parvaneh Rabiee, Patricia Sloper et al.•Health & Social Care in the…•2005

  • Social exclusion and access toleisure in Northern Ireland communities

    Ruth Jeanes, John Magee•Loisir et Société / Society and…•2010

  • Making choices in my life

    Open Access•Wendy Mitchell, Patricia Sloper•Children and Youth Services Review•2011

  • Parents' Emotional and Social Experiences of Caring for a Child Through Cleft Treatment

    Open Access•Pauline A Nelson, Pauline Nelson et al.•Qualitative Health Research•2012

  • Interacting With Providers

    Open Access•A Green, Penelope Abbott et al.•Qualitative Health Research•2018

  • Vulnerability in Inclusive Research

    Open Access•Rosemarie Van Den Breemer, Grete Arnesdatter Steigen et al.•International Journal of…•2024

  • The Quality of Care

    Avedis Donabedian•JAMA•1988

  • The Ethics of Social Research with Children

    Open Access•Virginia Morrow, Martin B Richards et al.•Children & Society•1996

  • Participatory Evaluation of Development Assistance

    Open Access•Claus C Rebien•Evaluation•1996

  • Parental Participation in Issues Concerning their Sons and Daughters with Learning Disabilities

    Danuta Orlowska•Disability & Society•1995

  • Quality of Life and Quality of Service Relationships

    Ruth Marquis, Robert L Jackson et al.•Disability & Society•2000

  • On the Edge

    Open Access•Ian Leedham•Health & Social Care in the…•2000

Obras citantes distintas17
Citas por año0,74
Intervalo de citas2003 - 2024 (22)
Velocidad de citaciónrecent
Altamente citadoNo
Tipos de citaNeutras: 17
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