All Stories

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