{"id":{"repo_id":"uoit","oai_identifier":"oai:ontariotechu.scholaris.ca:10155/1628"},"canonical_url":"https://search.dev.ndltd.org/etd/uoit/oai:ontariotechu.scholaris.ca:10155/1628","repository":{"repo_id":"uoit","name":"Ontario Institute of Technology","base_url":"https://ontariotechu.scholaris.ca/server/oai/request"},"display":{"title":"The psychosocial impact of surviving childhood cancer and reassimilating back into society in young adults","abstract":"Approximately 82% of children with childhood cancer survive at least 5 years after their diagnosis. Survivors are faced with a new reality and are faced with having to navigate that reality based on their own perspectives. While many facets encompassing survivorship have been explored in the literature, holistic approaches that evaluate the psychosocial impacts of surviving childhood cancer and how these impacts interact collectively are relatively few. The purpose of this study is to explore the psychosocial impact of surviving childhood cancer and reassimilation back into society in young adult survivors of childhood cancer utilizing qualitative methodology. A total of 4 participants participated in this study and shared their experience with childhood cancer, with 2 participants participating in the focus group discussion. The implication of this study makes an important contribution for survivors, healthcare providers, policymakers, and educators involved in survivorship and long-term care for survivors.","abstract_html":"Approximately 82% of children with childhood cancer survive at least 5 years after their diagnosis. Survivors are faced with a new reality and are faced with having to navigate that reality based on their own perspectives. While many facets encompassing survivorship have been explored in the literature, holistic approaches that evaluate the psychosocial impacts of surviving childhood cancer and how these impacts interact collectively are relatively few. The purpose of this study is to explore the psychosocial impact of surviving childhood cancer and reassimilation back into society in young adult survivors of childhood cancer utilizing qualitative methodology. A total of 4 participants participated in this study and shared their experience with childhood cancer, with 2 participants participating in the focus group discussion. The implication of this study makes an important contribution for survivors, healthcare providers, policymakers, and educators involved in survivorship and long-term care for survivors.","abstract_has_math":false,"creators":["Racine, Shanelle"],"institution":"University of Ontario Institute of Technology","degree_name":"Master of Health Sciences (MHSc)","degree_level":null,"degree_discipline":"Computer Science","degree_department":null,"school":null,"contributors":[],"advisors":["Sanchez, Otto"],"committee_chairs":[],"committee_members":[],"year":2023,"date_issued":"2023-05-01","date_published":"2023-05-01","updated_at":"2026-07-24T05:35:16Z","subjects":["Childhood cancer","Survivorship","Reassimilating","Psychosocial impact","Young adult"],"languages":["en"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/10155/1628","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Sanchez, Otto"]},{"key":"dc:creator","label":"Author","values":["Racine, Shanelle"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2023-05-09T20:16:21Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2023-05-09T20:16:21Z"]},{"key":"dc:date.issued","label":"Date","values":["2023-05-01"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Computer Science"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Health Sciences (MHSc)"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Ontario Institute of Technology"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Childhood cancer","Survivorship","Reassimilating","Psychosocial impact","Young adult"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://hdl.handle.net/10155/1628"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Approximately 82% of children with childhood cancer survive at least 5 years after their diagnosis. Survivors are faced with a new reality and are faced with having to navigate that reality based on their own perspectives. While many facets encompassing survivorship have been explored in the literature, holistic approaches that evaluate the psychosocial impacts of surviving childhood cancer and how these impacts interact collectively are relatively few. The purpose of this study is to explore the psychosocial impact of surviving childhood cancer and reassimilation back into society in young adult survivors of childhood cancer utilizing qualitative methodology. A total of 4 participants participated in this study and shared their experience with childhood cancer, with 2 participants participating in the focus group discussion. The implication of this study makes an important contribution for survivors, healthcare providers, policymakers, and educators involved in survivorship and long-term care for survivors."]},{"key":"dc:title","label":"Title","values":["The psychosocial impact of surviving childhood cancer and reassimilating back into society in young adults"]}]}],"canonical_facts":{"dc:contributor.advisor":["Sanchez, Otto"],"dc:creator":["Racine, Shanelle"],"dc:date.accessioned":["2023-05-09T20:16:21Z"],"dc:date.available":["2023-05-09T20:16:21Z"],"dc:date.issued":["2023-05-01"],"dc:description.abstract":["Approximately 82% of children with childhood cancer survive at least 5 years after their diagnosis. Survivors are faced with a new reality and are faced with having to navigate that reality based on their own perspectives. While many facets encompassing survivorship have been explored in the literature, holistic approaches that evaluate the psychosocial impacts of surviving childhood cancer and how these impacts interact collectively are relatively few. The purpose of this study is to explore the psychosocial impact of surviving childhood cancer and reassimilation back into society in young adult survivors of childhood cancer utilizing qualitative methodology. A total of 4 participants participated in this study and shared their experience with childhood cancer, with 2 participants participating in the focus group discussion. The implication of this study makes an important contribution for survivors, healthcare providers, policymakers, and educators involved in survivorship and long-term care for survivors."],"dc:identifier.uri":["https://hdl.handle.net/10155/1628"],"dc:language.iso":["en"],"dc:subject":["Childhood cancer","Survivorship","Reassimilating","Psychosocial impact","Young adult"],"dc:title":["The psychosocial impact of surviving childhood cancer and reassimilating back into society in young adults"],"dc:type":["Thesis"],"thesis:degree_discipline":["Computer Science"],"thesis:degree_name":["Master of Health Sciences (MHSc)"],"thesis:institution_name":["University of Ontario Institute of Technology"]},"updated_at":"2026-07-24T05:35:16Z"}