Skip to content

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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06229535
Enrollment
60
Registered
2024-01-29
Start date
2023-11-16
Completion date
2024-11-16
Last updated
2024-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oncologic Disorders

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Centro di Riferimento Oncologico - Aviano
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum

Inclusion criteria

* 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.

Exclusion criteria

NA

Design outcomes

Primary

MeasureTime frameDescription
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.up to 1 yearFrequency with which words attributable to the topic of awareness are expressed in the text
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.up to 1 yearFrequency 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 implications/implications perceived or experienced on one's present and future history with respect to the issue of the right to be forgotten.up to 1 yearFrequency 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.

Secondary

MeasureTime frameDescription
Frequency of patients with information that can lead to the recognition of the right to be forgotten primarily in the AYA populationup to 1 yearFrequency of patients with information that can lead to the recognition of the right to be forgotten primarily in the AYA population measured through indicators that identify this argumentative junction in the text

Countries

Italy

Contacts

Primary ContactMaurizio Mascarin, MD
mascarin@cro.it0434 659 536

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026