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Kate Oulton

Biographic Data

ID168183
NAMEKate Oulton
GIVEN NAMESKate
FAMILY NAMEOulton
SIGNATUREOULTON K
AFFILIATIONSGreat Ormond Street Hospital for Children NHS Foundation Trust
ORCID0000-0002-5778-3849
VERIFIEDYes
TOTAL WORKS7
TOTAL CITATIONS6
WORKS AS AUTHOR7
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2009
LATEST PUBLICATION YEAR2026
H-INDEX1
  • Engaging With Children

    Open Access•Faith Gibson, Jo Wray et al.•ARTICLE•Qualitative Health Research•2026

    This paper examines researchers’ use of visual methods and arts-based activities, when researching with children who have rare diseases, about their experiences of happiness, fulfilment, and resilience. Their perspectives were sought in order that a tailored ‘Bank of Happiness’ intervention be tested to investigate whether this approach could promote children’s wellbeing and resilience in this setting and applied more widely in the future. In thi…

  • The Forgotten Voices

    Open Access•Jo Wray, Jessica Russell et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: The importance of enabling patients to provide feedback on their experience of healthcare is widely accepted but there are few appropriate measures to enable children and young people to directly provide feedback, particularly those with intellectual disability or younger children. Our primary aim was to develop and test patient-reported experience measures for children and young people with intellectual disability who use inpatient h…

  • Online community engagement in response to Covid‐19 pandemic

    Open Access•Logan Manikam, Shereen Allaham et al.•ARTICLE•Health Expectations•2021

    Community participatory research is a method of active engagement between community members to develop interventions that catalyse social change and improve health outcomes.1 Increasingly, particularly in low-middle-income countries (LMICs), participatory research is used to co-develop low-cost community interventions. UK health policy and providers are also placing increasing emphasis on strengthening community services to equitably optimize hea…

  • Studying Children's Experiences in Interactions With Clinicians

    Open Access•Gemma Bryan, Myra Bluebond‐langner et al.•ARTICLE•Qualitative Health Research•2019•Cited by: 6•References: 31

    Increased emphasis on the child's voice and point of view in care and treatment has led to an expansion in the development of methods to access and identify their perspectives. Drawing on our experiences in a study of children with leukemia in hospital, this article explains the challenges and opportunities that arise in the use of five commonly used methods in a study of hospitalized children's experiences with health care professionals, includi…

  • Using participatory and creative research methods to develop and pilot an informative game for preparing children for blood tests

    Kate Oulton, Naomi Oldrieve et al.•ARTICLE•Arts & Health•2017•References: 2

    Background: . We sought to develop and evaluate a prototype “tool” to help prepare children for having their blood taken, a procedure most feared by children. Methods: A user-experience design, using creative arts was utilized. Twenty-three children aged 4–12 with haematological conditions participated. Phase 1 involved children developing a blood preparatory “tool” alongside an illustrator. Phase 2 involved children trialing a paper prototype of…

  • Healthcare professional and interpreter perspectives on working with and caring for non-English speaking families in a tertiary paediatric healthcare setting

    Anna Williams, Kate Oulton et al.•ARTICLE•Ethnicity and Health•2017•References: 3

    Our data show how significant the impact of language barriers can be, and the need to consider not only how communication can be improved, but also how this is situated in the specific context of tertiary paediatric care as well as a wider social context of inequity

  • Devoted protection

    Kate Oulton, Bob Heyman•ARTICLE•Health Risk & Society•2009

    This paper aims to explore the risk perceptions of parents caring for children who have severe learning disabilities and complex medical needs. The paper draws upon a qualitative study involving 20 parents, mostly mothers. The findings document the demanding care requirements which these parents had to meet. Parents viewed their role in terms of devoted vocation rather than meeting a burdensome obligation. This dedication interacted with heighten…

  • Studying Children's Experiences in Interactions With Clinicians

    Open Access•Gemma Bryan, Myra Bluebond‐langner et al.•ARTICLE•Qualitative Health Research•2019•Cited by: 6•References: 31

    Increased emphasis on the child's voice and point of view in care and treatment has led to an expansion in the development of methods to access and identify their perspectives. Drawing on our experiences in a study of children with leukemia in hospital, this article explains the challenges and opportunities that arise in the use of five commonly used methods in a study of hospitalized children's experiences with health care professionals, includi…

  • Devoted protection

    Kate Oulton, Bob Heyman•ARTICLE•Health Risk & Society•2009

    This paper aims to explore the risk perceptions of parents caring for children who have severe learning disabilities and complex medical needs. The paper draws upon a qualitative study involving 20 parents, mostly mothers. The findings document the demanding care requirements which these parents had to meet. Parents viewed their role in terms of devoted vocation rather than meeting a burdensome obligation. This dedication interacted with heighten…

  • Using participatory and creative research methods to develop and pilot an informative game for preparing children for blood tests

    Kate Oulton, Naomi Oldrieve et al.•ARTICLE•Arts & Health•2017•References: 2

    Background: . We sought to develop and evaluate a prototype “tool” to help prepare children for having their blood taken, a procedure most feared by children. Methods: A user-experience design, using creative arts was utilized. Twenty-three children aged 4–12 with haematological conditions participated. Phase 1 involved children developing a blood preparatory “tool” alongside an illustrator. Phase 2 involved children trialing a paper prototype of…

  • Healthcare professional and interpreter perspectives on working with and caring for non-English speaking families in a tertiary paediatric healthcare setting

    Anna Williams, Kate Oulton et al.•ARTICLE•Ethnicity and Health•2017•References: 3

    Our data show how significant the impact of language barriers can be, and the need to consider not only how communication can be improved, but also how this is situated in the specific context of tertiary paediatric care as well as a wider social context of inequity

  • Studying Children's Experiences in Interactions With Clinicians

    Open Access•Gemma Bryan, Myra Bluebond‐langner et al.•ARTICLE•Qualitative Health Research•2019•Cited by: 6•References: 31

    Increased emphasis on the child's voice and point of view in care and treatment has led to an expansion in the development of methods to access and identify their perspectives. Drawing on our experiences in a study of children with leukemia in hospital, this article explains the challenges and opportunities that arise in the use of five commonly used methods in a study of hospitalized children's experiences with health care professionals, includi…

  • Online community engagement in response to Covid‐19 pandemic

    Open Access•Logan Manikam, Shereen Allaham et al.•ARTICLE•Health Expectations•2021

    Community participatory research is a method of active engagement between community members to develop interventions that catalyse social change and improve health outcomes.1 Increasingly, particularly in low-middle-income countries (LMICs), participatory research is used to co-develop low-cost community interventions. UK health policy and providers are also placing increasing emphasis on strengthening community services to equitably optimize hea…

  • The Forgotten Voices

    Open Access•Jo Wray, Jessica Russell et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: The importance of enabling patients to provide feedback on their experience of healthcare is widely accepted but there are few appropriate measures to enable children and young people to directly provide feedback, particularly those with intellectual disability or younger children. Our primary aim was to develop and test patient-reported experience measures for children and young people with intellectual disability who use inpatient h…

  • Engaging With Children

    Open Access•Faith Gibson, Jo Wray et al.•ARTICLE•Qualitative Health Research•2026

    This paper examines researchers’ use of visual methods and arts-based activities, when researching with children who have rare diseases, about their experiences of happiness, fulfilment, and resilience. Their perspectives were sought in order that a tailored ‘Bank of Happiness’ intervention be tested to investigate whether this approach could promote children’s wellbeing and resilience in this setting and applied more widely in the future. In thi…

Medicine (5 works) · Psychology (5 works) · Medical education (4 works) · Sociology (4 works) · Nursing (3 works) · Political science (3 works) · Children's Rights and Participation (2 works) · Citizen journalism (2 works) · Developmental psychology (2 works) · Family medicine (2 works)

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