{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/81548"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/81548","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Information and the Management of Treatment in Chronic Illness: A Qualitative Study of People Living With HIV -Disease","abstract":"Transcripts from the in-depth interviews were coded to identify patterns relevant to the project research questions, and other artifacts collected or generated during fieldwork were used as supplementary evidence. Analysis revealed that participants rely extensively on health care providers and other individuals living with illness as sources of information and conduits for learning about their treatment regimens. Other information sources and activities tied closely to the individual and their surrounding personal environment, including past experience and bodily sensations, trial and error work, and the creation and maintenance of routines are also important, particularly when searching for ways to meaningfully integrate a new or altered treatment regimen into daily life. Finally, beyond gathering and using treatment-related information, participants also described making dedicated efforts to control the access that other people have to information regarding their treatment of HIV/AIDS. The implications of these findings for existing conceptualizations of health information, information seeking and use, and models of chronic illness management are examined.","abstract_html":"Transcripts from the in-depth interviews were coded to identify patterns relevant to the project research questions, and other artifacts collected or generated during fieldwork were used as supplementary evidence. Analysis revealed that participants rely extensively on health care providers and other individuals living with illness as sources of information and conduits for learning about their treatment regimens. Other information sources and activities tied closely to the individual and their surrounding personal environment, including past experience and bodily sensations, trial and error work, and the creation and maintenance of routines are also important, particularly when searching for ways to meaningfully integrate a new or altered treatment regimen into daily life. Finally, beyond gathering and using treatment-related information, participants also described making dedicated efforts to control the access that other people have to information regarding their treatment of HIV/AIDS. The implications of these findings for existing conceptualizations of health information, information seeking and use, and models of chronic illness management are examined.","abstract_has_math":false,"creators":["Hogan, Timothy P."],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Library and Information Science","degree_department":null,"school":null,"contributors":["Palmer, Carole L."],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-09-25T20:17:12Z","date_published":"2015-09-25T20:17:12Z","updated_at":"2026-07-22T22:26:16Z","subjects":["Health Sciences, General"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(MiAaPQ)AAI3290247"],"render_values":[{"text":"(MiAaPQ)AAI3290247","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/81548","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Palmer, Carole L."]},{"key":"dc:creator","label":"Author","values":["Hogan, Timothy P."]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2015-09-25T20:17:12Z","10000-01-01","2007"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Library and Information Science"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Health Sciences, General"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/81548","(MiAaPQ)AAI3290247"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Transcripts from the in-depth interviews were coded to identify patterns relevant to the project research questions, and other artifacts collected or generated during fieldwork were used as supplementary evidence. Analysis revealed that participants rely extensively on health care providers and other individuals living with illness as sources of information and conduits for learning about their treatment regimens. Other information sources and activities tied closely to the individual and their surrounding personal environment, including past experience and bodily sensations, trial and error work, and the creation and maintenance of routines are also important, particularly when searching for ways to meaningfully integrate a new or altered treatment regimen into daily life. Finally, beyond gathering and using treatment-related information, participants also described making dedicated efforts to control the access that other people have to information regarding their treatment of HIV/AIDS. The implications of these findings for existing conceptualizations of health information, information seeking and use, and models of chronic illness management are examined.","Made available in DSpace on 2015-09-25T20:17:12Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 3290247.pdf: 9344883 bytes, checksum: 46ab5f5dafdc3bb54cae91dfa53a37a0 (MD5) Previous issue date: 2007","Embargo set by: Seth Robbins for item 82829 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","348 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2007."]},{"key":"dc:title","label":"Title","values":["Information and the Management of Treatment in Chronic Illness: A Qualitative Study of People Living With HIV -Disease"]}]}],"canonical_facts":{"dc:contributor":["Palmer, Carole L."],"dc:creator":["Hogan, Timothy P."],"dc:date":["2015-09-25T20:17:12Z","10000-01-01","2007"],"dc:description":["Transcripts from the in-depth interviews were coded to identify patterns relevant to the project research questions, and other artifacts collected or generated during fieldwork were used as supplementary evidence. Analysis revealed that participants rely extensively on health care providers and other individuals living with illness as sources of information and conduits for learning about their treatment regimens. Other information sources and activities tied closely to the individual and their surrounding personal environment, including past experience and bodily sensations, trial and error work, and the creation and maintenance of routines are also important, particularly when searching for ways to meaningfully integrate a new or altered treatment regimen into daily life. Finally, beyond gathering and using treatment-related information, participants also described making dedicated efforts to control the access that other people have to information regarding their treatment of HIV/AIDS. The implications of these findings for existing conceptualizations of health information, information seeking and use, and models of chronic illness management are examined.","Made available in DSpace on 2015-09-25T20:17:12Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 3290247.pdf: 9344883 bytes, checksum: 46ab5f5dafdc3bb54cae91dfa53a37a0 (MD5) Previous issue date: 2007","Embargo set by: Seth Robbins for item 82829 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","348 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2007."],"dc:identifier":["http://hdl.handle.net/2142/81548","(MiAaPQ)AAI3290247"],"dc:language":["eng"],"dc:subject":["Health Sciences, General"],"dc:title":["Information and the Management of Treatment in Chronic Illness: A Qualitative Study of People Living With HIV -Disease"],"dc:type":["text"],"thesis:degree_discipline":["Library and Information Science"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:26:16Z"}