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Online information and support needs of young people with cancer: a participatory action research study
PURPOSE: The Internet is a fully integrated part of young people’s life and it is pivotal that online resources are developed to maximize the potential of the Internet to support those living with and beyond cancer. We sought to understand how young people with a cancer diagnosis use the Internet an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167089/ https://www.ncbi.nlm.nih.gov/pubmed/30310338 http://dx.doi.org/10.2147/AHMT.S173115 |
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author | Lea, Sarah Martins, Ana Morgan, Sue Cargill, Jamie Taylor, Rachel M Fern, Lorna A |
author_facet | Lea, Sarah Martins, Ana Morgan, Sue Cargill, Jamie Taylor, Rachel M Fern, Lorna A |
author_sort | Lea, Sarah |
collection | PubMed |
description | PURPOSE: The Internet is a fully integrated part of young people’s life and it is pivotal that online resources are developed to maximize the potential of the Internet to support those living with and beyond cancer. We sought to understand how young people with a cancer diagnosis use the Internet and to what extent information and support needs are met by existing online resources. PATIENTS AND METHODS: This was a participatory action research study involving 21 young people participating in workshops and individual interviews. Participants aged 13–24 years were diagnosed with a range of cancers. Young people were on treatment or had completed treatment; some had experienced relapse. Workshops consisted of participatory methods including focus group discussions, interactive activities, and individual thought, encompassing online resources used; when, how and what they were searching for, whether resources were helpful and how they could be improved. RESULTS: Young people reported using communication platforms, entertainment sites, social media, medical websites, charity websites, and search engines to find information and support. Different online use and needs were described throughout their cancer timeline and online use was generally driven by negative emotions. Seven factors influenced access and engagement: 1) where young people were on their cancer timeline; 2) external influencing factors, such as family and environments; 3) emotional drivers; 4) what young people search for online; 5) resources, websites, and digital platforms used by young people; 6) availability, accessibility, and assessment of online information and resources; 7) emotional responses to using online resources. CONCLUSION: The way young people access and engage with online resources is complex with multiple influencing factors including powerful emotional drivers and responses to Internet searching. There is a need to develop resources that support the holistic needs of young people and this should be done in collaboration with young people. |
format | Online Article Text |
id | pubmed-6167089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61670892018-10-11 Online information and support needs of young people with cancer: a participatory action research study Lea, Sarah Martins, Ana Morgan, Sue Cargill, Jamie Taylor, Rachel M Fern, Lorna A Adolesc Health Med Ther Original Research PURPOSE: The Internet is a fully integrated part of young people’s life and it is pivotal that online resources are developed to maximize the potential of the Internet to support those living with and beyond cancer. We sought to understand how young people with a cancer diagnosis use the Internet and to what extent information and support needs are met by existing online resources. PATIENTS AND METHODS: This was a participatory action research study involving 21 young people participating in workshops and individual interviews. Participants aged 13–24 years were diagnosed with a range of cancers. Young people were on treatment or had completed treatment; some had experienced relapse. Workshops consisted of participatory methods including focus group discussions, interactive activities, and individual thought, encompassing online resources used; when, how and what they were searching for, whether resources were helpful and how they could be improved. RESULTS: Young people reported using communication platforms, entertainment sites, social media, medical websites, charity websites, and search engines to find information and support. Different online use and needs were described throughout their cancer timeline and online use was generally driven by negative emotions. Seven factors influenced access and engagement: 1) where young people were on their cancer timeline; 2) external influencing factors, such as family and environments; 3) emotional drivers; 4) what young people search for online; 5) resources, websites, and digital platforms used by young people; 6) availability, accessibility, and assessment of online information and resources; 7) emotional responses to using online resources. CONCLUSION: The way young people access and engage with online resources is complex with multiple influencing factors including powerful emotional drivers and responses to Internet searching. There is a need to develop resources that support the holistic needs of young people and this should be done in collaboration with young people. Dove Medical Press 2018-09-17 /pmc/articles/PMC6167089/ /pubmed/30310338 http://dx.doi.org/10.2147/AHMT.S173115 Text en © 2018 Lea et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Lea, Sarah Martins, Ana Morgan, Sue Cargill, Jamie Taylor, Rachel M Fern, Lorna A Online information and support needs of young people with cancer: a participatory action research study |
title | Online information and support needs of young people with cancer: a participatory action research study |
title_full | Online information and support needs of young people with cancer: a participatory action research study |
title_fullStr | Online information and support needs of young people with cancer: a participatory action research study |
title_full_unstemmed | Online information and support needs of young people with cancer: a participatory action research study |
title_short | Online information and support needs of young people with cancer: a participatory action research study |
title_sort | online information and support needs of young people with cancer: a participatory action research study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167089/ https://www.ncbi.nlm.nih.gov/pubmed/30310338 http://dx.doi.org/10.2147/AHMT.S173115 |
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