Breadcrumb

Publications

Abrahao R et al., A qualitative study of barriers and facilitators to adolescents and young adults' participation in cancer clinical trials: Oncologist and patient perspectives.

Atwiine B et al.,  "Money was the problem": Caregivers' self-reported reasons for abandoning their children's cancer treatment in southwest Uganda.

Bates C et al., Psychosocial functioning of caregivers of pediatric brain tumor survivors.

Bisogno G et al., Role of centers with different patient volumes in the management of rhabdomyosarcoma. An analysis by the Italian Pediatric Soft Tissue Sarcoma Committee.

Bouchard E et al., Social media use and patient-provider relationships: Lessons for patients, caregivers, and healthcare providers.

Brosnan P et al., Psychosocial care providers' perspectives: Barriers to implementing services for siblings of children with cancer.

Canter K et al., A community-based trial of a psychosocial eHealth intervention for parents of children with cancer.

Cowfer B et al., Effect of time on quality of parent-child communication in pediatric cancer.

De Abreu Lourenco R et al., Understanding decisions to participate in genomic medicine in children's cancer care: A comparison of what influences parents, health care providers, and the general community.

Dunn T et al., Associations of job demands and patient safety event involvement on burnout among a multidisciplinary group of pediatric hematology/oncology clinicians.

Eche I et al., A systematic review and meta-analytic evaluation of psychosocial interventions in parents of children with cancer with an exploratory focus on minority outcomes.

Etkin-Spigelman L et al.,  Sharing psychosocial risk screening information with pediatric oncology healthcare providers: Service utilization and related factors.                     

Fardell J et al.,  Long-term health-related quality of life in young childhood cancer survivors and their parents.

Fleming C et al.,  Poor diet quality and adverse eating behaviors in young survivors of childhood cancer.

Greenzang K et al.,  Thinking ahead: Parents' worries about late effects of childhood cancer treatment.

Hancock K et al.,  A qualitative examination of the benefits and challenges of a psychosocial screening intervention in pediatric oncology: "Support comes to us".

Hjelmstedt S et al.,  Facilitators and barriers to return to work and meet financial needs in parents of children with cancer.

Iveus K et al.,  Family bonding as a result of the family talk intervention in pediatric oncology: Siblings' experiences.

Laronne A et al.,  "Some things are even worse than telling a child he is going to die": Pediatric oncology healthcare professionals perspectives on communicating with children about cancer and end of life.

Levitch C et al., Comparison of neuropsychological functioning in pediatric posterior fossa tumor survivors: Medulloblastoma, low-grade astrocytoma, and healthy controls.

McCarthy M et al., Parental adjustment following their child's completion of acute lymphoblastic leukemia treatment

Meryk A et al., Implementation of daily patient-reported outcome measurements to support children with cancer.

Moola F et al., Contemplating art and identity during a research study: Reflections on working with a youth with cancer.

Moscato E et al., Family functioning and adaptation following pediatric brain tumor: A systematic review.

Mueller E et al., The practical matters of including patient-reported outcomes in pediatric oncology clinical care.

Peterson R et al., Changes in executive function in pediatric brain tumor survivors.

Phillips C et al., Implementation science in pediatric oncology: A narrative review and future directions.

Posa S et al.,  Exploring illness identity among children and youth living with cancer: A narrative review.

Schaefer M et al.,  "Giving the gift of life twice": Understanding the lived experiences of parent donors and nondonors in pediatric haploidentical hematopoietic cell transplantation.

Schulte F et al.,  Social adjustment in survivors of acute lymphoblastic leukemia without cranial radiation therapy.

Sisk B et al., Interdependent functions of communication with adolescents and young adults in oncology

Szilagyi C et al.,  Interprofessional spiritual care education in pediatric hematology-oncology: A pilot study.

Warner E et al., Cancer content and social media platform influence young adult cancer caregivers' social support on social media

Winning A et al.,  Impact of central nervous system-directed treatment on competence and adjustment among children in early cancer survivorship.

Youn S et al.,  Neurocognitive and psychological functioning of pediatric brain tumor patients undergoing proton beam therapy for three different tumor types.

Zheng D et al.,  Disparities in pediatric psychosocial oncology utilization.

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