Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups. - Wikidata - awgldk - TriplyDB

Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups.

Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups.

http://www.wikidata.org/entity/Q30837465

about

Interventions for promoting participation in shared decision-making for children with cancer Current understanding of decision-making in adolescents with cancer: A narrative systematic review Furthering patient adherence: a position paper of the international expert forum on patient adherence based on an internet forum discussion.Online focus groups as a tool to collect data in hard-to-include populations: examples from paediatric oncology."I just forget to take it": asthma self-management needs and preferences in adolescents.Mixed feelings of children and adolescents with unilateral congenital below elbow deficiency: an online focus group study.Advantages of asynchronous online focus groups and face-to-face focus groups as perceived by child, adolescent and adult participants: a survey study.Opinions of youngsters with congenital below-elbow deficiency, and those of their parents and professionals concerning prosthetic use and rehabilitation treatment.Why parents refuse childhood vaccination: a qualitative study using online focus groups.Who decides? Decision making and fertility preservation in teens with cancer: a review of the literature.A good resource for parents, but will clinicians use it?: Evaluation of a resource for paediatric end-of-life decision making What Do Children with Chronic Diseases and Their Parents Think About Pediatricians? A Qualitative Interview Study.What is known about parents' treatment decisions? A narrative review of pediatric decision making.Adherence to medication: A nation-wide study from the Children's Cancer Hospital, Egypt.A Qualitative Study of Decision-Making on Phase III Randomized Clinical Trial Participation in Pediatric Oncology: Adolescents' and Parents' Perspectives and Preferences.Connecting with healthcare providers at diagnosis: adolescent/young adult cancer survivors' perspectives.Identifying a conceptual shift in child and adolescent-reported treatment decision making: "Having a say, as I need at this time".Parental trust in health care--a prospective study from the Children's Cancer Hospital in Egypt.Hypothesis generation for childhood cancer communication research: results of a secondary analysis.Communicating with child patients in pediatric oncology consultations: a vignette study on child patients', parents', and survivors' communication preferences.Parents' and Adolescents' Preferences for Intensified or Reduced Treatment in Randomized Lymphoblastic Leukemia Trials.Information-sharing between healthcare professionals, parents and children with cancer: more than a matter of information exchange.Parents' Challenges and Physicians' Tasks in Disclosing Cancer to Children. A Qualitative Interview Study and Reflections on Professional Duties in Pediatric Oncology.Do pediatric hematology/oncology (PHO) fellows receive communication training?Exploring young patients’ perspectives on rehabilitation care: methods and challenges of organizing focus groups for children and adolescents.Communication in pediatric oncology: State of the field and research agenda.Adolescent patient involvement in discussions about relapsed or refractory cancer with oncology clinicians.Reporting health-related quality of life scores to physicians during routine follow-up visits of pediatric oncology patients: is it effective?Parents' and Physicians' Perceptions of Children's Participation in Decision-making in Paediatric Oncology: A Quantitative Study.Improving Communication in Adolescent Cancer Care: A Multiperspective Study.Factors facilitating dementia case management: Results of online focus groups.Adolescent cancer patients' perceived quality of cancer care: The roles of patient engagement and supporting independence.Cancer, adolescence, and their peers: "they'll give you a story".'Just in case': the fertility information needs of teenagers and young adults with cancer.

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P2860

Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups.

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Jozien M Bensing

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P2860

Collecting behavioural data using the world wide web: considerations for researchers.

Partnerships with children.

Children as consumers.

Doctor-parent-child communication. A (re)view of the literature.

Essential elements of communication in medical encounters: the Kalamazoo consensus statement.

Managing communication with young people who have a potentially life threatening chronic illness: qualitative study of patients and parents.

Pediatric adherence as a multidimensional and dynamic construct, involving a triadic partnership.

Good communication in pediatric cancer care: a culturally-informed research agenda.

Supportive care needs of parents of children with cancer: transition from diagnosis to treatment.

Parental treatment decision making in pediatric oncology.

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