跳至主要内容
临床试验/NCT06229535
NCT06229535招募中不适用

The Right to be Forgotten in the AYA Population: Patients' Experience and Perspectives (Diritto All'Oblio)

Centro di Riferimento Oncologico - Aviano9 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年11月16日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
9
主要终点
Frequency of participants citing words attributable to the thematic area that delineate the architecture of the text about meaning and subjective perception of the right to be forgotten.

研究概览

简要总结

Cancer survivors experience a form of social discrimination that is described in numerous areas such as private life, educational and work paths and the achievement of personal goals. Starting from this scenario, more and more national legislative initiatives are emerging to reconcognize the right to be forgotten, defined as the right not to have to report one's, resolved, oncological disease in contact with institutions such as insurance companies, banks or others. The issue of the right to be forgotten is current and new, primarily in the AYA (adolescents and young adults) population. The purpose of this study is to explore and describe the experience of adolescents and young adults affected by previous oncological disease with respect to the issue of the right to be forgotten. In particular, focusing on:

  • awareness (knowledge of the issue);
  • significance attributed and subjective perception;
  • implications/fallouts perceived or experienced on one's present and future history.

详细描述

Cancer survivors experience a form of social discrimination that is described in numerous areas such as private life, educational and work paths and the achievement of personal goals. Starting from this scenario, more and more national legislative initiatives are emerging to reconcognize the right to be forgotten, defined as the right not to have to report one's, resolved, oncological disease in contact with institutions such as insurance companies, banks or others. The issue of the right to be forgotten is current and new, primarily in the AYA (adolescents and young adults) population. The purpose of this study is to explore and describe the experience of adolescents and young adults affected by previous oncological disease with respect to the issue of the right to be forgotten. In particular, focusing on:

  • awareness (knowledge of the issue);
  • significance attributed and subjective perception;
  • implications/fallouts perceived or experienced on one's present and future history.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age at diagnosis between (or equal to) 15 and 39 years;
  • patients not in active phase of treatment;
  • at least 5 years elapsed since diagnosis;
  • comprehension and written expressive ability of the Italian language.
  • subscription informed consent to the study.

排除标准

  • 未提供

结局指标

主要结局

Frequency of participants citing words attributable to the thematic area that delineate the architecture of the text about meaning and subjective perception of the right to be forgotten.

时间窗: up to 1 year

Frequency of participants citing words attributable to the thematic area that delineate the architecture of the text about meaning and subjective perception of the right to be forgotten.

Frequency of participants citing words attributable to the topic of awareness in the text with the aim to explore the experience of adolescents and young adults with prior cancer with respect to the issue of the right to be forgotten.

时间窗: up to 1 year

Frequency with which words attributable to the topic of awareness are expressed in the text

Frequency of participants citing words attributable to implications/implications perceived or experienced on one's present and future history with respect to the issue of the right to be forgotten.

时间窗: up to 1 year

Frequency of participants citing words attributable to implications/implications perceived or experienced on one's present and future history with respect to the issue of the right to be forgotten.

次要结局

  • Frequency of patients with information that can lead to the recognition of the right to be forgotten primarily in the AYA population(up to 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (9)

Loading locations...

相似试验