All Stories

  1. Understanding the importance of therapeutic alliance during physiotherapy treatment for musculoskeletal pain in children: a scoping review
  2. Children with cerebral palsy avoid stepping in potholes with mediolateral changes in foot placement that cause laterally instability
  3. Narrative Accounts of Youth and their Mothers with Chronic Headache
  4. Definition and Assessment of Paediatric Breakthrough Pain: A Qualitative Interview Study
  5. The Concept of Child-Centred Care in Healthcare: A Scoping Review
  6. Being Participatory Through Animation
  7. A rapid systematic review of breakthrough pain definitions and descriptions
  8. Parental sleep‐related practices and sleep in children aged 1–3 years: a systematic review
  9. A cross-sectional survey of healthcare professionals supporting children and young people with epilepsy and their parents/carers: which topics are raised in clinical consultations and can healthcare professionals provide the support needed?
  10. The Concept of Child-Centered Care in Healthcare: A Scoping Review
  11. “A hard-won capability”: the experiences of parents managing their babies' medicines after discharge from a neonatal unit
  12. How real-time images of the eardrum help parents and children make better decisions about care
  13. Designing a novel protocol to investigate mechanisms of falls in children with cerebral palsy, informed by lived experiences
  14. “I’d go slow and hope I don’t fall” Exploring lived experiences of children with cerebral palsy walking in challenging environments
  15. The economic burden experienced by carers of children who had a critical deterioration at a tertiary children’s hospital in the United Kingdom (the DETECT study): an online survey
  16. Developing rights-based standards for children having tests, treatments, examinations and interventions: using a collaborative, multi-phased, multi-method and multi-stakeholder approach to build consensus
  17. A shared love: reciprocity and hopefulness in romantic relationships of young adults with chronic pain
  18. Health literacy among children living with a long-term condition: ‘What I know and who I tell’
  19. Communication during children's X-ray procedures and children's experiences of the procedure: A scoping review
  20. Feeling stretched: Parents’ narratives about challenges to resilience when their child has a tracheostomy
  21. ‘ZOOMing’ in on Consulting with Children and Parents Remotely to Co-Create Health Information Resources
  22. Changing Agendas on Sleep, Treatment and Learning in Epilepsy (CASTLE) Sleep-E: a protocol for a randomised controlled trial comparing an online behavioural sleep intervention with standard care in children with Rolandic epilepsy
  23. A cross sectional study investigating dynamic balance when stepping to targets in children with cerebral palsy compared to typically developing children
  24. Dietary Therapy to Improve Nutrition and Gut Health in Paediatric Crohn’s Disease; A Feasibility Study
  25. OP029 [Emerging Sciences / Technology » Innovations]: THE CLINICAL EFFECTIVENESS OF DYNAMIC ELECTRONIC TRACKING AND ESCALATION TO REDUCE CRITICAL CARE TRANSFERS (THE DETECT STUDY)
  26. Unsettling the fluidity of practice and dealing with threat: the experiences of paediatric pharmacists in response to the admission of adult COVID-19 patients requiring intensive care in a paediatric tertiary hospital
  27. Parents supporting parents to reduce the risk of bronchiolitis (a respiratory virus)
  28. Clinical utility and acceptability of a whole-hospital, pro-active electronic paediatric early warning system (the DETECT study): A prospective e-survey of parents and health professionals
  29. Parents’/caregivers’ fears and concerns about their child’s epilepsy: A scoping review
  30. Navigating uncertain illness trajectories for young children with serious infectious illness: a modified grounded theory study
  31. Parents’ experiences and perceptions of the acceptability of a whole-hospital, pro-active electronic pediatric early warning system (the DETECT study): A qualitative interview study
  32. Health professionals’ initial experiences and perceptions of the acceptability of a whole-hospital, pro-active electronic paediatric early warning system (the DETECT study): a qualitative interview study
  33. ‘I feel like my house was taken away from me’ : Parents' experiences of having home adaptations for their medically complex, technology‐dependent child
  34. Changing Agendas on Sleep, Treatment and Learning in Epilepsy (CASTLE) Sleep-E: A protocol for a randomised controlled trial comparing an online behavioural sleep intervention with standard care in children with Rolandic epilepsy
  35. Multicentre, randomised controlled feasibility study to compare a 10-week physiotherapy programme using an interactive exercise training device to improve walking and balance, to usual care of children with cerebral palsy aged 4–18 years: the ACCEPT st...
  36. ‘It’s my back…’; developing the coming to spinal clinic resource to improve the health literacy of young people with adolescent idiopathic scoliosis and their parents
  37. ‘It doesn't feel like our house anymore’: The impact of medical technology upon life at home for families with a medically complex, technology-dependent child
  38. Defining usual physiotherapy care in ambulant children with cerebral palsy in the United Kingdom: A mixed methods consensus study
  39. “Communicating Lily’s Pain”: A reflective narrative commentary about co‐creating a resource to provoke thinking and change about assessing and managing the pain of children with profound cognitive impairment
  40. Healthcare Professionals’ Experiences of the Barriers and Facilitators to Pediatric Pain Management in the Community at End-of-Life: A Qualitative Interview Study
  41. Using an animation to enhance parents and professionals’ communication and assessment of pain in children with profound cognitive impairment
  42. Seeing lockdown through the eyes of children from around the world: Reflecting on a children's artwork project
  43. “Pain talk”: A triadic collaboration in which nurses promote opportunities for engaging children and their parents about managing children’s pain
  44. Using methods across generations: researcher reflections from a research project involving young people and their parents
  45. Ataxia and mobility in children following surgical resection of posterior fossa tumour: A longitudinal cohort study
  46. Navigating uncertain illness trajectories for young children with serious infectious illness: a mixed-methods modified grounded theory study
  47. Children and young people’s contributions to public involvement and engagement activities in health-related research: A scoping review
  48. Children’s pictures of COVID-19 and measures to mitigate its spread: An international qualitative study
  49. Is paediatric endotracheal suctioning by nurses' evidence based? An International Survey
  50. Paediatric Outpatient Parenteral Antimicrobial Therapy (OPAT): An e-survey of the experiences of parents and clinicians
  51. “People play it down and tell me it can’t kill people, but I know people are dying each day”. Children’s health literacy relating to a global pandemic (COVID-19); an international cross sectional study
  52. Two‐Stage Revision Hip Arthroplasty with or without the Use of an Interim Spacer for Managing Late Prosthetic Infection: A Systematic Review of the Literature
  53. The impact of digital educational interventions to support parents caring for acutely ill children at home and factors that affect their use: systematic review protocol (Preprint)
  54. Impact of Digital Educational Interventions to Support Parents Caring for Acutely Ill Children at Home and Factors That Affect Their Use: Protocol for a Systematic Review (Preprint)
  55. How nurses use reassurance to support the management of acute and chronic pain in children and young people: An exploratory, interpretative qualitative study
  56. Romantic Relationships in Young People with Long-Term Health Conditions: A Scoping Review
  57. Developing a Framework to Support the Delivery of Effective Pain Management for Children: An Exploratory Qualitative Study
  58. Crohn's and colitis: New research offers insights into caring for young people
  59. Depression, anxiety, and loneliness among adolescents and young adults with IBD in the UK: the role of disease severity, age of onset, and embarrassment of the condition
  60. Sustaining, Forming, and Letting Go of Friendships for Young People with Inflammatory Bowel Disease (IBD): A Qualitative Interview-Based Study
  61. Communication styles between family carers and children with leukaemia in occupied Palestinian territory
  62. A systematic review of the organizational, environmental, professional and child and family factors influencing the timing of admission to hospital for children with serious infectious illness
  63. Physical restraint of children and adolescents in mental health inpatient services: A systematic review and narrative synthesis
  64. Holding Their Own and Being Resilient: Narratives of Parents over the First 12 Months of Their Child Having Tracheostomy
  65. “I Don’t Like to Make a Big Thing out of It”: A Qualitative Interview-Based Study Exploring Factors Affecting Whether Young People Tell or Do Not Tell Their Friends about Their IBD
  66. Not a nurse but more than a mother: the everyday geographies of mothering children with complex heath care needs
  67. Experiencing place identity and place belongingness at a children’s hospice: Parents’ perspectives
  68. Stories as findings in collaborative research: making meaning through fictional writing with disadvantaged young people
  69. Communicating Pain: The Challenge of Pain Assessment in Children with Profound Cognitive Impairment
  70. Working back to the future: strengthening radical social work with children and young people, and their perspectives on resilience, capabilities and overcoming adversity
  71. Using participatory drama workshops to explore children’s beliefs, understandings and experiences of coming to hospital for clinical procedures
  72. Home-based treatment for a serious bacterial infection
  73. Exercise and Physical Therapy Interventions for Children with Ataxia: A Systematic Review
  74. “It’s a lifeline”: Generating a sense of social connectedness through befriending parents of disabled children or children with additional need
  75. Coming ‘Home’: Place bonding for parents accessing or considering hospice based respite
  76. Core Health Outcomes in Childhood Epilepsy (CHOICE): Development of a core outcome set using systematic review methods and a Delphi survey consensus
  77. The absent-present researcher: data analysis of pre-recorded parent-driven campaign videos
  78. Parent’s experiences of their child’s withdrawal syndrome: a driver for reciprocal nurse-parent partnership in withdrawal assessment
  79. Child Centred Care: Challenging Assumptions and Repositioning Children and Young People
  80. Can children be treated safely with parenteral antimicrobial therapy for serious bacterial infection
  81. Toward developing consensus on family-centred care: An international descriptive study and discussion
  82. New steps of change
  83. ‘Place bonding’ in children’s hospice care: a qualitative study
  84. International commentary on Phiri et al. ‘Registered nurses’ experiences pertaining to family involvement in the care of hospitalised children at a tertiary government hospital in Malawi’
  85. A review of literature about disfigurement, the body and clothing and accessories
  86. A qualitative study of health professionals’ views on the holding of children for clinical procedures: Constructing a balanced approach
  87. The practice of writing
  88. Evaluating a telehealth intervention for urinalysis monitoring in children with neurogenic bladder
  89. The concept of child-centered care in healthcare
  90. Inequality and poverty
  91. Holding children for procedures: An international survey of health professionals
  92. Being Participatory: Researching with Children and Young People
  93. Getting poetic with data: Using poetry to disseminate the first-person voices of parents of children with a disability
  94. A systematic evidence synthesis of interventions to engage children and young people in consultations about their long-term conditions
  95. Participatory Research: Does It Genuinely Extend the Sphere of Children’s and Young People’s Participation?
  96. Participatory Research in the Past, Present and Future
  97. Core Health Outcomes In Childhood Epilepsy (CHOICE): protocol for the selection of a core outcome set
  98. A sense of belonging: The importance of fostering student nurses’ affective bonds
  99. Parenting a Child With Complex Health Care Needs: A Stressful and Imposed “Clinical Career”
  100. Young children's experiences of growing up with a chronic illness
  101. Consulting with children, parents and a teacher to shape a qualitative study
  102. Using videos made by parent as part of a campaign to raise awareness
  103. Peer review: A good but flawed system?
  104. Parent-to-parent peer support for parents of children with a disability: A mixed method study
  105. Looking towards the horizon: changing landscapes and a shift to a more equitable future for children, young people and their families
  106. Getting published: Only one step in disseminating your findings
  107. Nursing judgement and decision-making using the Sedation Withdrawal Score (SWS) in children
  108. Creating authentic video scenarios for use in prehospital research
  109. Accuracy and Efficiency of Recording Pediatric Early Warning Scores Using an Electronic Physiological Surveillance System Compared With Traditional Paper-Based Documentation
  110. Developing a web-based resource for parents of young children undergoing day surgery
  111. Misleading information, exaggeration and the need to act
  112. Auto-driven Photo Elicitation Interviews in Research with Children: Ethical and Practical Considerations
  113. Optimizing Numeric Pain Rating Scale administration for children: The effects of verbal anchor phrases
  114. Developing a Sense of Knowing and Acquiring the Skills to Manage Pain in Children with Profound Cognitive Impairments: Mothers’ Perspectives
  115. Language, disfigurement, stigma and clothing
  116. In pursuit of an optimal model of undergraduate nurse clinical education: An integrative review
  117. Perseverance and parents of children with complex health care needs
  118. Parallel-Serial Memoing
  119. Pain experience, expression and coping in boys and young men with Duchenne Muscular Dystrophy – A pilot study using mixed methods
  120. Personal qualities necessary to care for people with dementia
  121. Is undernutrition prognostic of infection complications in children undergoing surgery? A systematic review
  122. “Knowing the Places of Care”: How Nurses Facilitate Transition of Children with Complex Health Care Needs from Hospital to Home
  123. The Impact of Immersive Outdoor Activities in Local Woodlands on Young Carers Emotional Literacy and Well-Being
  124. Navigating Uncertainty: Health Professionals’ Knowledge, Skill, and Confidence in Assessing and Managing Pain in Children with Profound Cognitive Impairment
  125. Social relationships, loneliness and adolescence
  126. Holding Children for Clinical Procedures: Perseverance in Spite of or Persevering to be Child-Centered
  127. The context, influences and challenges for undergraduate nurse clinical education: Continuing the dialogue
  128. Transition
  129. Generic training will not prepare nurses of right calibre to care for children and families
  130. Support for Children’s Protagonism
  131. ‘If you see something, say something’
  132. Bladder augmentation in children and young adults: a review of published literature
  133. Motivational Interviewing Post-Stroke
  134. Young women with a disorder of sex development: learning to share information with health professionals, friends and intimate partners about bodily differences and infertility
  135. Parents’ and children’s beliefs and concerns about taking medicines
  136. Identifying Continence OptioNs after Stroke (ICONS): an evidence synthesis, case study and exploratory cluster randomised controlled trial of the introduction of a systematic voiding programme for patients with urinary incontinence after stroke in seco...
  137. A Qualitative Study of Communication between Young Women with Disorders of Sex Development and Health Professionals
  138. ‘We don't have recipes; we just have loads of ingredients’: explanations of evidence and clinical decision making by speech and language therapists
  139. Technology adoption in health care
  140. Identifying continence options after stroke (ICONS): a cluster randomised controlled feasibility trial
  141. Misunderstood as mothers: women's stories of being hospitalized for illness in the postpartum period
  142. Advancing health and well-being through children’s rights
  143. Service user involvement in practitioner education: Movement politics and transformative change
  144. Holding and restraining children for clinical procedures within an acute care setting: an ethical consideration of the evidence
  145. Parenting a sick child
  146. Be my guest! Challenges and practical solutions of undertaking interviews with children in the home setting
  147. How arts-based approaches can put the fun into child-focused research
  148. Development and validation of the Liverpool infant bronchiolitis severity score: a research protocol
  149. Child poverty
  150. ‘Just kids playing sport (in a chair)’: experiences of children, families and stakeholders attending a wheelchair sports club
  151. ‘Being a presence’
  152. The assessment and management of children's pain
  153. The restrictions to the use of codeine and dilemmas about safe alternatives
  154. Paediatric intensive care nurses' and doctors' perceptions on nurse-led protocol-directed ventilation weaning and extubation
  155. Parents’ experiences and views of caring for a child with a tracheostomy: A literature review
  156. Looking for an ordinary life
  157. Modernising health visiting practice whilst keeping compassion in care
  158. Stigma, health and incarceration
  159. ‘I am closer to this place’—Space, place and notions of home in lived experiences of hospice day care
  160. ‘Do I, don’t I ask for help?’
  161. Researching children's health experiences: The place for participatory, child-centered, arts-based approaches
  162. Editorial
  163. Editorial
  164. Editorial
  165. A UK and Irish survey of enteral nutrition practices in paediatric intensive care units
  166. Parents need to protect: influences, risks and tensions for parents of prepubertal children born with ambiguous genitalia
  167. Children’s well-being: Priorities and considerations
  168. Reflections on the ethics of Internet newsgroup research
  169. Developing and Implementing an Appreciative ‘Quality of Care’ Approach to Child Neglect Practice
  170. The Identification of Acute Stroke: An Analysis of Emergency Calls
  171. Autobiography as genre for qualitative data: A reservoir of experience for nursing research
  172. Home-Based Care for Special Healthcare Needs
  173. Social support for mothers in illness: A multifaceted phenomenon
  174. FUNdamentally important: humour and fun as caring and practice
  175. Deconstructing child and adolescent mental health: questioning the‘taken-for-granted’…
  176. Searching for harmony: parents’ narratives about their child’s genital ambiguity and reconstructive genital surgeries in childhood
  177. Assessment of acute pain in children: development of evidence-based guidelines
  178. Key Working for Families with Young Disabled Children
  179. Editorial: A day at the beach or …
  180. Time-use diaries are acceptable to parents with a disabled preschool child and are helpful in understanding families' daily lives
  181. A structured observation of the interaction between nurses and patients during the administration of medication in an acute mental health unit
  182. Mothering disrupted by illness: a narrative synthesis of qualitative research
  183. Addressing end of life care issues in a tertiary treatment centre: lessons learned from surveying parents’ experiences
  184. Appropriated landscapes: the intrusion of technology and equipment into the homes and lives of families with a child with complex needs
  185. A simple act?
  186. Taking a deep breath . . . or two ... or three?
  187. Living with type 1 diabetes: perceptions of children and their parents
  188. Tick box for child? The ethical positioning of children as vulnerable, researchers as barbarians and reviewers as overly cautious
  189. Re-visioning the doctoral research degree in nursing in the United Kingdom
  190. Examining the British PhD viva: Opening new doors or scarring for life?
  191. Fear, failure, outrage and grief: the dissonance between public outrage and individual action?
  192. Editorial: Nursing amidst stories (and knowing what to do with them)
  193. Parents’ narratives about their experiences of their child's reconstructive genital surgeries for ambiguous genitalia
  194. Global health: time for a safer, fairer world
  195. What pain assessment guidelines tell us and what they may miss
  196. Commentary on Shields L, Pratt J & Hunter J (2006) Family centred care: a review of qualitative studies. Journal of Clinical Nursing 5, 1317-23
  197. Analgesia Review
  198. Pain Assessment
  199. Medical Procedures
  200. Postoperative pain
  201. Background
  202. Quick reference summary of recommendations and good practice points
  203. ‘Good’ and ‘bad’ stories: decisive moments, ‘shock and awe’ and being moral
  204. The influence of culture on diabetes self-management: perspectives of Gujarati Muslim men who reside in northwest England
  205. Guidance, Guidance Everywhere, but One you Need to Read: 0-18 years: guidance for all doctors
  206. Bunny hops and creative thinking about getting youngsters active
  207. Percutaneous Endoscopic Gastrostomy Feeding in Nursing Homes
  208. Parenting: a glut of information
  209. An exploration of best practice in multi-agency working and the experiences of families of children with complex health needs. What works well and what needs to be done to improve practice for the future?
  210. Children in handcuffs and detained behind bars. Where in the world?
  211. Kicking Eeyore into touch: ‘Living-strong’, ‘nursing-strong’ and being appreciative and solution-focused
  212. Chronic pain in children and adolescents
  213. Far away and close to home... stones, stories and health care
  214. Weight monitoring of breastfed babies in the United Kingdom - interpreting, explaining and intervening
  215. APPRECIATING WHAT WORKS: DISCOVERING AND DREAMING ALONGSIDE PEOPLE DEVELOPING RESILIENT SERVICES FOR YOUNG PEOPLE REQUIRING MENTAL HEALTH SERVICES
  216. ‘One expertise among many’— working appreciatively to make miracles instead of finding problems
  217. Thingamijigs, wotsits and the naming of things
  218. A letter to myself - stay angry, keep caring...
  219. From Peter, Jane and Tiptoes to literacy as freedom
  220. Weight monitoring of breastfed babies in the UK - centile charts, scales and weighing frequency
  221. “They’ve got to be as good as mum and dad”: Children with complex health care needs and their siblings’ perceptions of a Diana community nursing service
  222. A spoonful of sugar helps the medicine go down...
  223. Evaluating Student Paediatric Advanced Nurse Practitioners’ Experiences of a Paediatric Pharmacology Module: In the Context of Reflective Learning
  224. If I have to Say it One more Time, I Swear I’m Gonna Kill Someone
  225. Touching the Void – Taking Decisions and Finding Solutions
  226. Pain narratives and narrative practitioners: a way of working ’in-relation’ with children experiencing pain
  227. ‘Bloods Taken, CXR Later, No Change’
  228. Ducks Might Quack... Children and Domestic Violence in Rural Areas
  229. Bernie,... do you know what?
  230. Methodological issues and complementary therapies: researching intangibles?
  231. If you've `Gone Busted' - A Nurse will Fix you
  232. Think Child, Not Refugee
  233. It’s Dead …it Doesn’t Work Anymore, but will it Get Better?
  234. A pain workshop: an approach to eliciting the views of young people with chronic pain
  235. Clients' experiences of frozen shoulder and its treatment with Bowen technique
  236. The transition of adolescents with diabetes from the children's health care service into the adult health care service: a review of the literature
  237. Big Elephants Fighting Whilst Children’s Policy Misses Out?
  238. Adaptation and negotiation as an approach to care in paediatric diabetes specialist nursing practice: a critical review
  239. Dealing with uncertainty: parental assessment of pain in their children with profound special needs
  240. On ’Irafs and Other Amazing Things …
  241. Health Inequalities: A Blight on Children’s Lives and Futures
  242. An evaluation of a children's drug therapy service
  243. Chronic Pain in Childhood and the Medical Encounter: Professional Ventriloquism and Hidden Voices
  244. A pilot study to evaluate the effectiveness of Bowen Technique in the management of clients with frozen shoulder
  245. Ways of working: CCNs and chronic illness
  246. Reflections of a cynical optimist
  247. So-knit 1, purl 1… clone1?
  248. Childhood Chronic Illness: a continuing challenge
  249. Children - silent consumers of health care
  250. Public health for children: the Green Paper
  251. Children's health care: a new era or more rhetoric?
  252. Children's nursing-a cause for celebration
  253. Children's nurses as critical thinkers
  254. An asthmatic in‘Wonderland’: a patient's perspective of Accident and Emergency
  255. Complementary therapies and management of chronic pain
  256. Nursing Care and Management of Children's Perioperative Pain