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Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea
Objective: Caregivers may experience positive or negative feelings about their role. The study investigated the determinants of the burden and positivity of family caregivers of Korean terminal cancer patients. Methods: A multicenter cross‐sectional survey was conducted with 139 family caregivers. D...
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Published in: | Psycho-oncology (Chichester, England) England), 2012-03, Vol.21 (3), p.282-290 |
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creator | Park, Chang-Hae Shin, Dong Wook Choi, Jin Young Kang, Jina Baek, Young Ji Mo, Ha Na Lee, Mee-Sook Park, Seon-Ju Park, Sang Min Park, Sohee |
description | Objective: Caregivers may experience positive or negative feelings about their role. The study investigated the determinants of the burden and positivity of family caregivers of Korean terminal cancer patients.
Methods: A multicenter cross‐sectional survey was conducted with 139 family caregivers. Determinants of caregiver's burden and positivity were assessed by the Caregiver Reaction Assessment Scale and by three questions based on a previous study, respectively. Two separate hierarchical multiple regression models were used.
Results: Each domain of the caregiver's burden and positivity was explained by different factors, with the total explained variance ranging between 14.4–33.6% and 2.6–18.3%, respectively. Caregivers who were unmarried, less educated, and/or had low incomes were more likely to be negatively affected, while those who shared caregiving responsibilities were less prone to negative consequences. Caregivers who were male, religious practitioners, and who perceived a higher burden of schedule disruptions were more likely to have a positive perception of their role, while those who perceived a lack of family support were less likely.
Conclusions: Our results highlight the importance of sharing the caregiving burden with the other family members. Organizing a family meeting can provide an opportunity for other family members to acknowledge the feelings and reactions of the primary caregivers, and can prompt the sharing of caregiving responsibilities. Copyright © 2010 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/pon.1893 |
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Methods: A multicenter cross‐sectional survey was conducted with 139 family caregivers. Determinants of caregiver's burden and positivity were assessed by the Caregiver Reaction Assessment Scale and by three questions based on a previous study, respectively. Two separate hierarchical multiple regression models were used.
Results: Each domain of the caregiver's burden and positivity was explained by different factors, with the total explained variance ranging between 14.4–33.6% and 2.6–18.3%, respectively. Caregivers who were unmarried, less educated, and/or had low incomes were more likely to be negatively affected, while those who shared caregiving responsibilities were less prone to negative consequences. Caregivers who were male, religious practitioners, and who perceived a higher burden of schedule disruptions were more likely to have a positive perception of their role, while those who perceived a lack of family support were less likely.
Conclusions: Our results highlight the importance of sharing the caregiving burden with the other family members. Organizing a family meeting can provide an opportunity for other family members to acknowledge the feelings and reactions of the primary caregivers, and can prompt the sharing of caregiving responsibilities. Copyright © 2010 John Wiley & Sons, Ltd.</description><identifier>ISSN: 1057-9249</identifier><identifier>EISSN: 1099-1611</identifier><identifier>DOI: 10.1002/pon.1893</identifier><identifier>PMID: 22383270</identifier><identifier>CODEN: POJCEE</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Adult ; Aged ; Burden ; cancer ; caregiver ; Caregivers ; Caregivers - psychology ; Carers ; Caretaker syndrome ; Cost of Illness ; Emotions ; Families & family life ; Family - psychology ; Female ; Humans ; Male ; Middle Aged ; Oncology ; Polls & surveys ; Positive affect ; positivity ; Relatives ; Republic of Korea ; Responsibilities ; Role ; Self Concept ; Terminal illnesses ; Terminally Ill ; Terminally ill people</subject><ispartof>Psycho-oncology (Chichester, England), 2012-03, Vol.21 (3), p.282-290</ispartof><rights>Copyright © 2010 John Wiley & Sons, Ltd.</rights><rights>Copyright John Wiley and Sons, Limited Mar 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5173-fa7b0e8d652afa60b0b71ca3b804c14a6321bf090c50df4030f4a16b2b4385a23</citedby><cites>FETCH-LOGICAL-c5173-fa7b0e8d652afa60b0b71ca3b804c14a6321bf090c50df4030f4a16b2b4385a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,30999,31000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22383270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Chang-Hae</creatorcontrib><creatorcontrib>Shin, Dong Wook</creatorcontrib><creatorcontrib>Choi, Jin Young</creatorcontrib><creatorcontrib>Kang, Jina</creatorcontrib><creatorcontrib>Baek, Young Ji</creatorcontrib><creatorcontrib>Mo, Ha Na</creatorcontrib><creatorcontrib>Lee, Mee-Sook</creatorcontrib><creatorcontrib>Park, Seon-Ju</creatorcontrib><creatorcontrib>Park, Sang Min</creatorcontrib><creatorcontrib>Park, Sohee</creatorcontrib><title>Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea</title><title>Psycho-oncology (Chichester, England)</title><addtitle>Psycho-Oncology</addtitle><description>Objective: Caregivers may experience positive or negative feelings about their role. The study investigated the determinants of the burden and positivity of family caregivers of Korean terminal cancer patients.
Methods: A multicenter cross‐sectional survey was conducted with 139 family caregivers. Determinants of caregiver's burden and positivity were assessed by the Caregiver Reaction Assessment Scale and by three questions based on a previous study, respectively. Two separate hierarchical multiple regression models were used.
Results: Each domain of the caregiver's burden and positivity was explained by different factors, with the total explained variance ranging between 14.4–33.6% and 2.6–18.3%, respectively. Caregivers who were unmarried, less educated, and/or had low incomes were more likely to be negatively affected, while those who shared caregiving responsibilities were less prone to negative consequences. Caregivers who were male, religious practitioners, and who perceived a higher burden of schedule disruptions were more likely to have a positive perception of their role, while those who perceived a lack of family support were less likely.
Conclusions: Our results highlight the importance of sharing the caregiving burden with the other family members. Organizing a family meeting can provide an opportunity for other family members to acknowledge the feelings and reactions of the primary caregivers, and can prompt the sharing of caregiving responsibilities. Copyright © 2010 John Wiley & Sons, Ltd.</description><subject>Adult</subject><subject>Aged</subject><subject>Burden</subject><subject>cancer</subject><subject>caregiver</subject><subject>Caregivers</subject><subject>Caregivers - psychology</subject><subject>Carers</subject><subject>Caretaker syndrome</subject><subject>Cost of Illness</subject><subject>Emotions</subject><subject>Families & family life</subject><subject>Family - psychology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Polls & surveys</subject><subject>Positive affect</subject><subject>positivity</subject><subject>Relatives</subject><subject>Republic of Korea</subject><subject>Responsibilities</subject><subject>Role</subject><subject>Self Concept</subject><subject>Terminal illnesses</subject><subject>Terminally Ill</subject><subject>Terminally ill people</subject><issn>1057-9249</issn><issn>1099-1611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><recordid>eNqFkU1rFTEUhkNR2loL_gIZ3NTN1HxnspRWr2JpFW0LbkIyc6Kp89Vkpnr_vRnutYKgrnLgfc4TOC9CTwg-JhjTF-PQH5NKsx20T7DWJZGEPFhmoUpNud5Dj1K6wTjDWu6iPUpZxajC-yicwgSxC73tp1QMvpi-QuHm2EBf2L4pxiGFKdyFab2E3nahXRe1jfAl3EHcbGz22xyEts1hX0MsRjsFWJyhL94NEexj9NDbNsHh9j1Al69ffTp5U55drN6evDwra0EUK71VDkPVSEGttxI77BSpLXMV5jXhVjJKnMca1wI3nmOGPbdEOuo4q4Sl7AAdbbxjHG5nSJPpQqqhbW0Pw5yMppIILiTP5PN_koRWGdSakv-jmLJ8Ws4X9Nkf6M0wx3yf5etKc6aU-O2r45BSBG_GGDob19lklkpNrtQslWb06dY3uw6ae_BXhxkoN8D30ML6ryLz_uJ8K9zyIU3w45638ZuRiilhrs9XRn2Qn1erj1dGsZ9r3rjC</recordid><startdate>201203</startdate><enddate>201203</enddate><creator>Park, Chang-Hae</creator><creator>Shin, Dong Wook</creator><creator>Choi, Jin Young</creator><creator>Kang, Jina</creator><creator>Baek, Young Ji</creator><creator>Mo, Ha Na</creator><creator>Lee, Mee-Sook</creator><creator>Park, Seon-Ju</creator><creator>Park, Sang Min</creator><creator>Park, Sohee</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>ASE</scope><scope>FPQ</scope><scope>K6X</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201203</creationdate><title>Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea</title><author>Park, Chang-Hae ; Shin, Dong Wook ; Choi, Jin Young ; Kang, Jina ; Baek, Young Ji ; Mo, Ha Na ; Lee, Mee-Sook ; Park, Seon-Ju ; Park, Sang Min ; Park, Sohee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5173-fa7b0e8d652afa60b0b71ca3b804c14a6321bf090c50df4030f4a16b2b4385a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Burden</topic><topic>cancer</topic><topic>caregiver</topic><topic>Caregivers</topic><topic>Caregivers - psychology</topic><topic>Carers</topic><topic>Caretaker syndrome</topic><topic>Cost of Illness</topic><topic>Emotions</topic><topic>Families & family life</topic><topic>Family - psychology</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Polls & surveys</topic><topic>Positive affect</topic><topic>positivity</topic><topic>Relatives</topic><topic>Republic of Korea</topic><topic>Responsibilities</topic><topic>Role</topic><topic>Self Concept</topic><topic>Terminal illnesses</topic><topic>Terminally Ill</topic><topic>Terminally ill people</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Chang-Hae</creatorcontrib><creatorcontrib>Shin, Dong Wook</creatorcontrib><creatorcontrib>Choi, Jin Young</creatorcontrib><creatorcontrib>Kang, Jina</creatorcontrib><creatorcontrib>Baek, Young Ji</creatorcontrib><creatorcontrib>Mo, Ha Na</creatorcontrib><creatorcontrib>Lee, Mee-Sook</creatorcontrib><creatorcontrib>Park, Seon-Ju</creatorcontrib><creatorcontrib>Park, Sang Min</creatorcontrib><creatorcontrib>Park, Sohee</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Psycho-oncology (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Chang-Hae</au><au>Shin, Dong Wook</au><au>Choi, Jin Young</au><au>Kang, Jina</au><au>Baek, Young Ji</au><au>Mo, Ha Na</au><au>Lee, Mee-Sook</au><au>Park, Seon-Ju</au><au>Park, Sang Min</au><au>Park, Sohee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea</atitle><jtitle>Psycho-oncology (Chichester, England)</jtitle><addtitle>Psycho-Oncology</addtitle><date>2012-03</date><risdate>2012</risdate><volume>21</volume><issue>3</issue><spage>282</spage><epage>290</epage><pages>282-290</pages><issn>1057-9249</issn><eissn>1099-1611</eissn><coden>POJCEE</coden><abstract>Objective: Caregivers may experience positive or negative feelings about their role. The study investigated the determinants of the burden and positivity of family caregivers of Korean terminal cancer patients.
Methods: A multicenter cross‐sectional survey was conducted with 139 family caregivers. Determinants of caregiver's burden and positivity were assessed by the Caregiver Reaction Assessment Scale and by three questions based on a previous study, respectively. Two separate hierarchical multiple regression models were used.
Results: Each domain of the caregiver's burden and positivity was explained by different factors, with the total explained variance ranging between 14.4–33.6% and 2.6–18.3%, respectively. Caregivers who were unmarried, less educated, and/or had low incomes were more likely to be negatively affected, while those who shared caregiving responsibilities were less prone to negative consequences. Caregivers who were male, religious practitioners, and who perceived a higher burden of schedule disruptions were more likely to have a positive perception of their role, while those who perceived a lack of family support were less likely.
Conclusions: Our results highlight the importance of sharing the caregiving burden with the other family members. Organizing a family meeting can provide an opportunity for other family members to acknowledge the feelings and reactions of the primary caregivers, and can prompt the sharing of caregiving responsibilities. Copyright © 2010 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>22383270</pmid><doi>10.1002/pon.1893</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Burden cancer caregiver Caregivers Caregivers - psychology Carers Caretaker syndrome Cost of Illness Emotions Families & family life Family - psychology Female Humans Male Middle Aged Oncology Polls & surveys Positive affect positivity Relatives Republic of Korea Responsibilities Role Self Concept Terminal illnesses Terminally Ill Terminally ill people |
title | Determinants of the burden and positivity of family caregivers of terminally ill cancer patients in Korea |
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