Katherine Knighting

Publications

• Improving end of life care in care homes; an evaluation of the six steps to success programme
• Practitioners as Rule Using Analysts: A Further Development of Process Knowledge in Social Work
• Development of the Carers’ Alert Thermometer for Young Carers (CAT-YC) to Identify and Screen the Support Needs of Young Carers: A Mixed Method Consensus Study
• What does effective end-of-life care at home for children look like? A qualitative interview study exploring the perspectives of bereaved parents
• Sensitive, Challenging, and Difficult Topics: Experiences and Practical Considerations for Qualitative Researchers
• A different way of life: a qualitative study on the experiences of family caregivers of stroke survivors living at home
• Cognitive behavioural approaches for managing dyspnoea in people with chronic obstructive pulmonary disease (COPD)
• Bereavement support and Prolonged Grief Disorder amongst family carers of people with Motor Neuron Disease: views of health and social care professionals from a descriptive survey
• Paramedics and their role in end-of-life care: perceptions and confidence.
• Using a rapid appraisal approach in a nation-wide, multi-site public involvement study in Scotland.
• The engagement of young people in their own advance care planning process: A systematic narrative synthesis
• Continuing Bonds With Children and Bereaved Young People: A Narrative Review
• A Network Approach to Neonatal Palliative Care Education
• The use of digital legacies with people affected by motor neurone disease for continuing bonds: An interpretative phenomenological analysis study
• A qualitative study of health care professionals’ views and experiences of paediatric advance care planning
• Home-based end of life care for children and their families – a systematic scoping review and narrative synthesis
• Nurse-led cognitive behavioural therapy for respiratory patients.
• The Carers’ Alert Thermometer (CAT): supporting family carers of people living with Motor Neurone Disease.
• Views and experiences of young people, their parents/carers and healthcare professionals of the advance care planning process: A summary of the findings from a qualitative study
• A realist evaluation of a home-based end of life care service for children and families: what works, for whom, how, in what circumstances and why?
• Reflexivity and the development of process knowledge in social work: A classification and empirical study
• Comparative hypothesis assessment and quasi triangulation as process knowledge assessment strategies in social work practice
• Practitioners as Rule Using Analysts: A Further Development of Process Knowledge in Social Work
• Patient access to healthcare services and optimisation of self-management for ethnic minority populations living with diabetes: a systematic review.
• Short break and emergency respite care: what options for young people with life-limiting conditions?
• Gaining consensus on family carer needs when caring for someone dying at home to develop the Carers' Alert Thermometer (CAT): a modified Delphi study.
• Development of the Carers' Alert Thermometer (CAT) to identify family carers struggling with caring for someone dying at home: a mixed method consensus study.
• Children's understanding of cancer and views on health-related behaviour: a 'draw and write' study.
• Prioritization of future research topics for children's hospice care by its key stakeholders: a Delphi study.
• Exploring the experiences and perspectives of families using a children's hospice and professionals providing hospice care to identify future research priorities for children's hospice care.
• Engaging patients in health care: an empirical study of the role of engagement on attitudes and action.
• Student nurse non-attendance in relation to academic performance and progression
• Research priorities for respiratory nursing: a UK-wide Delphi study
• Meeting the needs of young adults with life-limiting conditions: A UK survey of current provision and future challenges for hospices
• The specification, acceptability and effectiveness of respite care and short breaks for young adults with complex healthcare needs: protocol for a mixed-methods systematic review
• A study of childhood cancer survivors' engagement with long-term follow-up care: ‘To attend or not to attend, that is the question’
• Respite care and short breaks for young adults aged 18–40 with complex health-care needs: mixed-methods systematic review and conceptual framework development
• Development of the Carers’ Alert Thermometer for Stroke Family Caregivers (CAT-S): A Multiphase Action Research Study
• Meeting the needs of young adults with life‐limiting conditions: A UK survey of current provision and future challenges for hospices
• Using the Carers’ Alert Thermometer tool to identify needs and support family caregivers of people with motor neurone disease: moving beyond needs assessments
• A UK survey on the experience and views of Respiratory Nurses (RNs) on their role in delivering Cognitive Behavioural Therapy (CBT) for patients with Chronic Obstructive Pulmonary Disease
• Development of the Carers' Alert Thermometer (CAT) to identify family carers struggling with caring for someone dying at home: a mixed method consensus study
• Gaining consensus on family carer needs when caring for someone dying at home to develop the Carers’ Alert Thermometer (CAT): A modified Delphi study.
• A scoping exercise to explore the current perceptions and attitudes of UK paramedics towards their role in the management of End of Life Care patients, in the pre-hospital setting
• Empowering Care Home Staff to Deliver Quality End of Life Care: The Impact of the Six Steps to Success Programme on End of Life Care in Care Homes in North West England
• Investigating the use of digital legacies with people affected by Motor Neurone Disease (Poster Presentation- Second Place Prize)
• Paramedics and their role in end-of-life care: perceptions and confidence
• Continuing Bonds with Children and Bereaved Young People: A Narrative Review
• The Carers’ Alert Thermometer (CAT): identifying the support needs of family carers of people living with Motor Neurone Disease
• The Carers’ Alert Thermometer (CAT): Identifying The Support Needs Of Family Carers Of People Living With MND (plwMND)
• Clarity through the Kaleidoscope: Gaining Consensus on the Main Causes of Carer Burden from Professional and Carer Perspectives
• Six Steps to Success Programme: Improving End of Life Care for Care Home Residents
• Bereavement support needs of family carers of people with Motor Nerone Disease (MND)
• Exploring experience and awareness of bereavement support in family carers of people with MND.
• "Support is too fragmented": the bereavement needs of carers and the presence of Prolonged Grief Disorder.
• Exploring the experience of pre and post-bereavement support in carers of those living with terminal illness: a small-scale, mixed-methods study.
• The Carers' Alert Thermometer (CAT): an instrument to identify the family carers' needs whilst providing end of life care in the home
• Bereavement support for family carers of people living with Motor Neurone Disease
• Emergency Care Impact Assessment (ECIA) Project: Exploring the impact of children’s hospice services upon hospice users and stakeholders.
• Predicting extreme grief response: Can health and social care professionals be helped to identify family carers of people with Motor Neurone Disease at risk of Prolonged Grief Disorder?
• "No other choice” when children’s hospice care is unavailable: An Emergency Care Impact Assessment for Claire House Children’s Hospice
• CP1- Investigating the use of digital legacies with people affected by MND (Poster Presentation)
• Meeting the needs of young adults with life-limiting conditions: A UK survey of current provision and future challenges for hospices.
• Research priorities for respiratory nursing
• Digital legacies with people affected by motor neurone disease: The views, experiences and perceptions of healthcare professionals, specialists and experts for use with bereaved young people.
• A Study of Childhood Cancer Survivors’ Engagement with Long-Term Follow-Up Care: ‘To attend or not to attend, that is the question’.
• The lived experiences of aunts and uncles supporting parents of children and young adults with Autism Spectrum Disorder (ASD): An interpretative phenomenological analysis study (Symposium Poster)
• Development of the Carers’ Alert Thermometer for Young Carers (CAT‑YC) to Identify and Screen the Support Needs of Young Carers: A Mixed Method Consensus Study
• Caring for Carers: Identifying the needs of family carer and improving support across Lancashire and South Cumbria with the Carers' Alert Thermometer for Stroke (CAT-S)
• Using a rapid appraisal approach in a nation-wide, multi-site public involvement study in Scotland.
• Who cares? A prospective study to develop an alert system for informal carers
• Children’s understanding of cancer and views on health related behaviour: a “draw and write” study.
• Prioritisation of future research topics for children’s hospice care by its key stakeholders: a Delphi study.
• Engaging patients in health care: An empirical study of the role of engagement on attitudes and action.
• Exploring the experiences and perspectives of families using a children’s hospice and professionals providing hospice care to identify future research priorities for children’s hospice care.
• Patient access to healthcare services and optimisation of self-management for ethnic minority populations living with diabetes: a systematic review
• Comparative Hypothesis Assessment and Quasi Triangulation as Process Knowledge Assessment Strategies in Social Work Practice
• Reflexivity and the development of process knowledge in social work: a classification and empirical study