跳至主要内容
临床试验/DRKS00029141
DRKS00029141招募中未知

Culture-sensitive communication in pediatric oncology - KuseKiO

Klinik für Kinder-Onkologie, -Hämatologie und klinische Immunologie am Universitätsklinikum Düsseldorf0 个研究点目标入组 80 人开始时间: 2022年6月13日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
0 Years 至 17 Years(—)
性别
All

入选标准

  • Pillar A: Included are underage patients and their families in life-changing conversations who are being treated at the Clinic for Paediatric Oncology, Haematology and Clinical Immunology and who have at least one of the following characteristics. 1:
  • 1. the language predominantly spoken in the family is not German.
  • 2. at least one parent, grandparent or great-grandparent of the child was not born in Germany (4th generation).
  • The selection of cases should be as contrasting as possible in order to obtain a broad picture of different needs (on the part of doctors and families) and culturally conditioned aspects in A-E-P discussions. If possible, 10 families with different migration histories (with/without language barriers, grandchildren of guest workers, children/grandchildren of ethnic German immigrants, children from families who have recently fled, etc.) should be observed and interviewed in order to filter out commonalities and differences in needs and communication challenges in the context of the corresponding conversations.
  • Pillar B: The inclusion criteria for the intervention study are to be formulated on the basis of the results of the status-quo analysis in Pillar A and therefore cannot yet be named.

排除标准

  • Adult patients. For participation in the study, the consent of both the underaged patient and both legal guardians is required. Consent should be available for adolescents aged 14 years and older. A missing consent of one of the described participants is an exclusion criterion for the participation in the study.
  • For the underage patients aged 8-13 years, consent is also sought, but it must be checked to what extent they can assess the significance and scope of the study. This must be decided on a case-by-case basis. For patients under 8 years of age, written consent is not required, but age-appropriate information and consent should be provided.
  • In addition, the responsible physicians will have to decide on a case-by-case basis whether organizational, personal or situational factors stand in the way of accompanying the consultation.

研究者

发起方
Klinik für Kinder-Onkologie, -Hämatologie und klinische Immunologie am Universitätsklinikum Düsseldorf

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