Psychosocial assessment as a standard of care in pediatric cancer

Kazak, Anne E., Abrams, Annah N., Banks, Jaime, Christofferson, Jennifer, DiDonato, Stephen, Grootenhuis, Martha A., Kabour, Marianne, Madan‐Swain, Avi +3 more·2015·Pediatric Blood & Cancer

Cited by (262)

Items 101–200 of 262

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  4. Quality of life and family functioning 12 months after diagnosis of childhood brain tumour: A longitudinal cohort study
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  5. Delivering Care Consistent With the Psychosocial Standards—Provider Report: Implementing the Standards Together—Engaging Parents and Providers in Psychosocial Care (iSTEPPP) Study
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    Annelienke M. van Hulst, Emma J. Verwaaijen, Marta F. Fiocco, Saskia M.F. Pluijm, Martha Alexandra Grootenhuis, Rob Pieters, Erica L T van den Akker, Marry M. van den Heuvel‐Eibrink · 2021 · BMC Pediatrics
  7. Psychosocial needs of pediatric cancer patients and their caregivers at end of treatment: Why psychosocial screening remains important
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  8. Health-related quality of life and its determinants during and after treatment for paediatric acute lymphoblastic leukaemia: a national, prospective, longitudinal study in the Netherlands
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  9. Predicting Quality of Life in Caregivers of Children with Cancer Within One Year Post-Diagnosis
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  10. Parent Perspectives after the PRISM-P Randomized Trial: A Mixed-Methods Analysis
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  11. Psychologists as Pivotal Members of the Pediatric Palliative Care Team
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  13. Checking IN : Development, Acceptability, and Feasibility of a Pediatric Electronic Distress Screener
    Lori S. Wiener, Sima Zadeh Bedoya, Mallorie L. Gordon, Abigail Fry, Robert Casey, Amii C. Steele, Kathy Ruble, Devon Ciampa, Maryland Pao · 2022 · Clinical Practice in Pediatric Psychology
  14. Poor Mental Health Among Survivors of Childhood Cancer—Risk Factors and a Call for Intervention
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  15. Risk factors for steroid‐induced affective disorder in children with leukemia
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  16. “Taking back control together”: Definition of a new intervention designed to support parents confronted with childhood cancer
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  17. The development of fatigue after treatment for pediatric brain tumors does not differ between tumor locations
    Elin Irestorm, Antoinette Y. N. Schouten‐van Meeteren, Marloes van Gorp, Jos W. R. Twisk, Hanneke Margo van Santen, Marita Partanen, Martha Alexandra Grootenhuis, Raphaële R. L. van Litsenburg · 2024 · Pediatric Blood & Cancer
  18. Patterns of family relationships in pediatric oncology: implications for children’s adjustment upon treatment completion
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  19. Psychosocial functioning of caregivers of pediatric brain tumor survivors
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  20. Developing the Evidence Base in Pediatric Oncology Nursing Practice for Promoting Health-Related Quality of Life in Pediatric Oncology Patients
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  21. Psychosocial Risk Profiles Among American and Dutch Families Affected by Pediatric Cancer
    Christina M. Sharkey, Sasja A. Schepers, Sarah Drake, Ahna L. H. Pai, Larry L. Mullins, Martha Alexandra Grootenhuis · 2020 · Journal of Pediatric Psychology
  22. Psychosocial services for pediatric oncology patients in low‐ and middle‐income countries from health care providers' perspectives: A survey‐based report from the SIOP Global Health Network Psychosocial Working Group
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  23. Barriers to Care and Perceived Need for Mental Health Services Among Adolescent and Emerging Adult Survivors of Pediatric Brain Tumors
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  24. Quality-of-Life Assessment in Pediatric Advanced Cancer: Development of the Patient-Reported Outcome Measure Advance QoL
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  25. Match of psychosocial risk and psychosocial care in families of a child with cancer
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  26. Conducting Psychosocial Intervention Research among Adolescents and Young Adults with Cancer: Lessons from the PRISM Randomized Clinical Trial
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  27. Hospitalization and mortality outcomes in the first 5 years after a childhood cancer diagnosis: a population-based study
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  29. Exploring Barriers and Inequalities in Access to Comprehensive Care for Pediatric Oncology Patients: A Systematic Review
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  30. Effects of childhood cancer on family functioning: A mixed-methods study from parental perspective
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  31. Benchmarking the pediatric quality of life (PedsQL) cancer module in a large Dutch national cohort of childhood cancer patients
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  33. Quality of life and family functioning soon after paediatric brain tumour diagnosis: A cross-sectional observational study
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  34. A Structured Template for Social Work Psychosocial Assessments and Formulations in Healthcare
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  35. Using formative evaluation to plan for electronic psychosocial screening in pediatric oncology
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  36. Early trajectory of psychosocial risk in families of children and adolescents newly diagnosed with cancer
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  37. Understanding the multilevel factors influencing the implementation of digital health interventions for supportive care in Adolescents and Young Adult (AYA) cancer survivorship: determinants of adopting mindfulness-based mobile applications
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  38. Implementing a Psychosocial Screener in Pediatric Oncology: Perspectives of Multidisciplinary Clinicians
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  42. Quality of self-report coping measures for children and adolescents with cancer: A systematic review.
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