All Stories

  1. Evaluating the efficacy of a mobile epilepsy education package application developed for the parents/caregivers of children with epilepsy in Canada
  2. Social Networks of Adolescents and Young Adults with Cancer: A Cross-Sectional Study
  3. Use of Virtual Reality in the Pediatric Perioperative Setting and for Induction of Anesthesia: Mixed Methods Pilot Feasibility Study
  4. Pediatric Oncology Knowledge Mobilization in Canada: An Environmental Scan Protocol (Preprint)
  5. Pediatric Oncology Knowledge Mobilization in Canada: An Environmental Scan Protocol (Preprint)
  6. Ethical Considerations for Children Undergoing Surgery: Evaluation of Graduate Nursing Students’ Learning
  7. Ophthalmological screening guidelines for individuals with Osteogenesis Imperfecta: a scoping review
  8. Building partnerships for novel and ethical netnographical approaches to monitor online communities in nursing
  9. The Design, Development, and Usability Testing of an eHealth Program for Youths With Osteogenesis Imperfecta: Protocol for a 2-Phase User-Centered Mixed Methods Study
  10. Childhood Worldings of Brittle Bone Disease: A Portrait in 5 Triptych Research Poem
  11. The Design, Development, and Usability Testing of an eHealth Program for Youths With Osteogenesis Imperfecta: Protocol for a 2-Phase User-Centered Mixed Methods Study (Preprint)
  12. Use of Netnography to Understand GoFundMe® Crowdfunding Profiles Posted for Individuals and Families of Children with Osteogenesis Imperfecta
  13. The moral experiences of children with osteogenesis imperfecta
  14. The use of virtual reality during medical procedures in a pediatric orthopedic setting: A mixed‐methods pilot feasibility study
  15. Use of virtual reality in managing paediatric procedural pain and anxiety: An integrative literature review
  16. Developing an mHealth Application to Coordinate Nurse-Provided Respite Care Services for Families Coping With Palliative-Stage Cancer: Protocol for a User-Centered Design Study
  17. Developing an mHealth Application to Coordinate Nurse-Provided Respite Care Services for Families Coping With Palliative-Stage Cancer: Protocol for a User-Centered Design Study (Preprint)
  18. Experiences of Children With Osteogenesis Imperfecta in the Co-design of the Interactive Assessment and Communication Tool Sisom OI: Secondary Analysis of Qualitative Design Sessions
  19. An Ethnographic Study of the Moral Experiences of Children with Cancer in New Delhi, India
  20. Giving Children With Osteogenesis Imperfecta a Voice: Participatory Approach for the Development of the Interactive Assessment and Communication Tool Sisom OI
  21. Experiences of Children With Osteogenesis Imperfecta in the Co-design of the Interactive Assessment and Communication Tool Sisom OI: Secondary Analysis of Qualitative Design Sessions (Preprint)
  22. Cover Images
  23. Bladder and bowel symptoms experienced by children with osteogenesis imperfecta
  24. Bladder and bowel symptoms experienced by children with osteogenesis imperfecta
  25. The day‐to‐day experiences of caring for children with Osteogenesis Imperfecta: A qualitative descriptive study
  26. Clinical manifestations of osteogenesis imperfecta in adulthood: An integrative review of quantitative studies and case reports
  27. Giving Children With Osteogenesis Imperfecta a Voice: Participatory Approach for the Development of the Interactive Assessment and Communication Tool Sisom OI (Preprint)
  28. Exploring the Views of Osteogenesis Imperfecta Caregivers on Internet-Based Technologies: Qualitative Descriptive Study
  29. Exploring the Views of Osteogenesis Imperfecta Caregivers on Internet-Based Technologies: Qualitative Descriptive Study (Preprint)
  30. Development of the Good2Go MyHealth Passport for individuals with Osteogenesis Imperfecta: A knowledge-synthesis study
  31. “Tell it as it is”: How Sisom prompts children and parents to discuss their cancer experience
  32. iCanCope PostOp: User-Centered Design of a Smartphone-Based App for Self-Management of Postoperative Pain in Children and Adolescents
  33. A pilot study to determine out‐of‐pocket expenditures by families of children being treated for cancer at public hospitals in New Delhi, India
  34. Validation of the Adolescent Pediatric Pain Tool for the Multidimensional Measurement of Pain in Children and Adolescents Diagnosed with Osteogenesis Imperfecta
  35. A qualitative study of the costs experienced by caregivers of children being treated for cancer in New Delhi, India
  36. A Best Practice Initiative to Optimize Transfer of Young Adults With Osteogenesis Imperfecta From Child to Adult Healthcare Services
  37. iCanCope PostOp: User-Centered Design of a Smartphone-Based App for Self-Management of Postoperative Pain in Children and Adolescents (Preprint)
  38. Exploring the Student Peer Mentor's Experience in a Nursing Peer Mentorship Program
  39. Usability Testing of an Interactive Communication Tool to Help Children Express Their Cancer Symptoms
  40. Pain and quality of life of children and adolescents with osteogenesis imperfecta over a bisphosphonate treatment cycle
  41. Pain experiences of adults with osteogenesis imperfecta: An integrative review
  42. The Impact of a Childhood Cancer Diagnosis on the Children and Siblings’ School Attendance, Performance, and Activities: A Qualitative Descriptive Study
  43. Distraction Kits for Pain Management of Children Undergoing Painful Procedures in the Emergency Department: A Pilot Study
  44. Exploring Mentees' Perceptions of an Undergraduate Nurse Peer Mentorship Program
  45. Pain Experiences of Children and Adolescents With Osteogenesis Imperfecta
  46. Validation of the scale on Satisfaction of Adolescents with Postoperative pain management-idiopathic Scoliosis (SAP-S)
  47. Linguistic Validation of an Interactive Communication Tool to Help French-Speaking Children Express Their Cancer Symptoms
  48. An Integrative Review of Peer Mentorship Programs for Undergraduate Nursing Students
  49. The psychosocial experience of individuals living with osteogenesis imperfecta: a mixed-methods systematic review
  50. Young Adults’ Perceptions of the Venturing Out Pack Program as a Tangible Cancer Support Service
  51. Quality of life in osteogenesis imperfecta: A mixed‐methods systematic review
  52. Balancing Illness and Parental Demands: 
Coping With Cancer While Raising Minor Children
  53. Usability Testing of a Computerized Communication Tool in a Diverse Urban Pediatric Population
  54. The magnitude and predictors of abandonment of therapy in paediatric acute leukaemia in middle-income countries: A systematic review and meta-analysis
  55. Determining the Costs of Families’ Support Networks Following a Child’s Cancer Diagnosis
  56. A mixed method approach to describe the out‐of‐pocket expenses incurred by families of children with cancer
  57. Abandonment of treatment for childhood cancer: position statement of a SIOP PODC Working Group
  58. A prospective study to determine the costs incurred by families of children newly diagnosed with cancer in Ontario
  59. Tele‐practice guidelines for the symptom management of children undergoing cancer treatment
  60. The cost of childhood cancer from the family's perspective: A critical review
  61. The costs children incur during treatment for cancer: a neglected area in theory and research
  62. Quality of life of children following bone marrow transplantation: critical review of the research literature