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Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan
We constructed a concise multidimensional care burden scale that reflects circumstances unique to Japan, with a focus on intractable neurological diseases. We surveyed 646 family caregivers of patients with intractable neurological diseases or stroke using 28 preliminary care burden scale items obta...
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Published in: | Health and quality of life outcomes 2006-08, Vol.4 (1), p.52-52, Article 52 |
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creator | Miyashita, Mitsunori Yamaguchi, Aki Kayama, Mami Narita, Yugo Kawada, Norikazu Akiyama, Miki Hagiwara, Akiko Suzukamo, Yoshimi Fukuhara, Shunichi |
description | We constructed a concise multidimensional care burden scale that reflects circumstances unique to Japan, with a focus on intractable neurological diseases. We surveyed 646 family caregivers of patients with intractable neurological diseases or stroke using 28 preliminary care burden scale items obtained from qualitative research. The results were used to finalize the feeling of care burden scale (BIC: burden index of caregivers), and verify its reliability and validity.
The survey was conducted among caregivers providing home health care to patients with intractable neurological diseases (PD [Parkinson's disease], SCD [spinocerebellar degeneration], MSA [multiple system atrophy], and ALS [amyotrophic lateral sclerosis]) or CVA (cerebrovascular accident) using a mailed, self-administered questionnaire between November, 2003 and May, 2004.
Response rates for neurological and CVA caregivers were 50% and 67%, respectively, or 646 in total (PD, 279; SCD, 78; MSA, 39; ALS, 30; and CVA, 220). Item and exploratory factor analyses led to a reduction to 11 items, comprising 10 items from the 5 domains of time-dependent burden, emotional burden, existential burden, physical burden, and service-related burden; and 1 item on total burden. Examination of validity showed a moderate correlation between each domain of the BIC and the SF-8 (Health related quality of life scale, Short Form-8), while the correlation coefficient of the overall BIC and CES-D was 0.62. Correlation between the BIC and ZBI, a preexisting care burden scale, was high (r = 0.84), while that with the time spent on providing care was 0.47. The ICC (Intraclass correlation coefficient) by test-retest reliability was 0.83, and 0.68 to 0.80 by individual domain.
These results show that the BIC, a new care burden scale comprising 11 items, is highly reliable and valid. |
doi_str_mv | 10.1186/1477-7525-4-52 |
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The survey was conducted among caregivers providing home health care to patients with intractable neurological diseases (PD [Parkinson's disease], SCD [spinocerebellar degeneration], MSA [multiple system atrophy], and ALS [amyotrophic lateral sclerosis]) or CVA (cerebrovascular accident) using a mailed, self-administered questionnaire between November, 2003 and May, 2004.
Response rates for neurological and CVA caregivers were 50% and 67%, respectively, or 646 in total (PD, 279; SCD, 78; MSA, 39; ALS, 30; and CVA, 220). Item and exploratory factor analyses led to a reduction to 11 items, comprising 10 items from the 5 domains of time-dependent burden, emotional burden, existential burden, physical burden, and service-related burden; and 1 item on total burden. Examination of validity showed a moderate correlation between each domain of the BIC and the SF-8 (Health related quality of life scale, Short Form-8), while the correlation coefficient of the overall BIC and CES-D was 0.62. Correlation between the BIC and ZBI, a preexisting care burden scale, was high (r = 0.84), while that with the time spent on providing care was 0.47. The ICC (Intraclass correlation coefficient) by test-retest reliability was 0.83, and 0.68 to 0.80 by individual domain.
These results show that the BIC, a new care burden scale comprising 11 items, is highly reliable and valid.</description><identifier>ISSN: 1477-7525</identifier><identifier>EISSN: 1477-7525</identifier><identifier>DOI: 10.1186/1477-7525-4-52</identifier><identifier>PMID: 16919162</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Aged ; Caregivers - psychology ; Cost of Illness ; Female ; Home Nursing - psychology ; Humans ; Japan ; Male ; Middle Aged ; Nervous System Diseases - classification ; Nervous System Diseases - nursing ; Psychometrics - instrumentation ; Quality of Life ; Spouses - psychology ; Stress, Psychological - diagnosis ; Stroke - nursing ; Surveys and Questionnaires</subject><ispartof>Health and quality of life outcomes, 2006-08, Vol.4 (1), p.52-52, Article 52</ispartof><rights>Copyright © 2006 Miyashita et al; licensee BioMed Central Ltd. 2006 Miyashita et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b578t-ebbc9653968c0cb4d8d0912c243390df066372aecd8e131e5f45da7315ceca213</citedby><cites>FETCH-LOGICAL-b578t-ebbc9653968c0cb4d8d0912c243390df066372aecd8e131e5f45da7315ceca213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563455/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1563455/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16919162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyashita, Mitsunori</creatorcontrib><creatorcontrib>Yamaguchi, Aki</creatorcontrib><creatorcontrib>Kayama, Mami</creatorcontrib><creatorcontrib>Narita, Yugo</creatorcontrib><creatorcontrib>Kawada, Norikazu</creatorcontrib><creatorcontrib>Akiyama, Miki</creatorcontrib><creatorcontrib>Hagiwara, Akiko</creatorcontrib><creatorcontrib>Suzukamo, Yoshimi</creatorcontrib><creatorcontrib>Fukuhara, Shunichi</creatorcontrib><title>Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan</title><title>Health and quality of life outcomes</title><addtitle>Health Qual Life Outcomes</addtitle><description>We constructed a concise multidimensional care burden scale that reflects circumstances unique to Japan, with a focus on intractable neurological diseases. We surveyed 646 family caregivers of patients with intractable neurological diseases or stroke using 28 preliminary care burden scale items obtained from qualitative research. The results were used to finalize the feeling of care burden scale (BIC: burden index of caregivers), and verify its reliability and validity.
The survey was conducted among caregivers providing home health care to patients with intractable neurological diseases (PD [Parkinson's disease], SCD [spinocerebellar degeneration], MSA [multiple system atrophy], and ALS [amyotrophic lateral sclerosis]) or CVA (cerebrovascular accident) using a mailed, self-administered questionnaire between November, 2003 and May, 2004.
Response rates for neurological and CVA caregivers were 50% and 67%, respectively, or 646 in total (PD, 279; SCD, 78; MSA, 39; ALS, 30; and CVA, 220). Item and exploratory factor analyses led to a reduction to 11 items, comprising 10 items from the 5 domains of time-dependent burden, emotional burden, existential burden, physical burden, and service-related burden; and 1 item on total burden. Examination of validity showed a moderate correlation between each domain of the BIC and the SF-8 (Health related quality of life scale, Short Form-8), while the correlation coefficient of the overall BIC and CES-D was 0.62. Correlation between the BIC and ZBI, a preexisting care burden scale, was high (r = 0.84), while that with the time spent on providing care was 0.47. The ICC (Intraclass correlation coefficient) by test-retest reliability was 0.83, and 0.68 to 0.80 by individual domain.
These results show that the BIC, a new care burden scale comprising 11 items, is highly reliable and valid.</description><subject>Aged</subject><subject>Caregivers - psychology</subject><subject>Cost of Illness</subject><subject>Female</subject><subject>Home Nursing - psychology</subject><subject>Humans</subject><subject>Japan</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nervous System Diseases - classification</subject><subject>Nervous System Diseases - nursing</subject><subject>Psychometrics - instrumentation</subject><subject>Quality of Life</subject><subject>Spouses - psychology</subject><subject>Stress, Psychological - diagnosis</subject><subject>Stroke - nursing</subject><subject>Surveys and Questionnaires</subject><issn>1477-7525</issn><issn>1477-7525</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp1kk1v1DAQhiNERUvhyhH5hKhEir8TX5DaFdCtKnEBrpY_Jruuknixkwr-fROyKl2hnmy9884zM5opijcEnxNSy4-EV1VZCSpKXgr6rDh5EJ4_-h8XL3O-xZgySsWL4phIRRSR9KQIP00bvBlC7FFs0LAFdDkmDz1a9x5-z9rKJNiEO0gZvb9cr84-IIO6sR2CDx30eco0LcrbmAbkJiuyS352pgXUpNiha7Mz_aviqDFthtf797T48eXz99VVefPt63p1cVNaUdVDCdY6JQVTsnbYWe5rjxWhjnLGFPYNlpJV1IDzNRBGQDRceFMxIhw4Qwk7LdYL10dzq3cpdCb90dEE_VeIaaNNGoJrQSvLm4YIjyvHOZbW1kaBlaoRihIv_cT6tLB2o-3AO-iHZNoD6GGkD1u9iXeaCMm4EBPgYgHYEJ8AHEZc7PS8Nj2vTXMt6MR4t28ixV8j5EF3ITtoW9NDHLOWdT01X83FzhejSzHnBM1DHYL1fC3_k98-Hu-ffX8e7B4aG7vt</recordid><startdate>20060818</startdate><enddate>20060818</enddate><creator>Miyashita, Mitsunori</creator><creator>Yamaguchi, Aki</creator><creator>Kayama, Mami</creator><creator>Narita, Yugo</creator><creator>Kawada, Norikazu</creator><creator>Akiyama, Miki</creator><creator>Hagiwara, Akiko</creator><creator>Suzukamo, Yoshimi</creator><creator>Fukuhara, Shunichi</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><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>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20060818</creationdate><title>Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan</title><author>Miyashita, Mitsunori ; Yamaguchi, Aki ; Kayama, Mami ; Narita, Yugo ; Kawada, Norikazu ; Akiyama, Miki ; Hagiwara, Akiko ; Suzukamo, Yoshimi ; Fukuhara, Shunichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b578t-ebbc9653968c0cb4d8d0912c243390df066372aecd8e131e5f45da7315ceca213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Caregivers - psychology</topic><topic>Cost of Illness</topic><topic>Female</topic><topic>Home Nursing - psychology</topic><topic>Humans</topic><topic>Japan</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nervous System Diseases - classification</topic><topic>Nervous System Diseases - nursing</topic><topic>Psychometrics - instrumentation</topic><topic>Quality of Life</topic><topic>Spouses - psychology</topic><topic>Stress, Psychological - diagnosis</topic><topic>Stroke - nursing</topic><topic>Surveys and Questionnaires</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyashita, Mitsunori</creatorcontrib><creatorcontrib>Yamaguchi, Aki</creatorcontrib><creatorcontrib>Kayama, Mami</creatorcontrib><creatorcontrib>Narita, Yugo</creatorcontrib><creatorcontrib>Kawada, Norikazu</creatorcontrib><creatorcontrib>Akiyama, Miki</creatorcontrib><creatorcontrib>Hagiwara, Akiko</creatorcontrib><creatorcontrib>Suzukamo, Yoshimi</creatorcontrib><creatorcontrib>Fukuhara, Shunichi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Health and quality of life outcomes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miyashita, Mitsunori</au><au>Yamaguchi, Aki</au><au>Kayama, Mami</au><au>Narita, Yugo</au><au>Kawada, Norikazu</au><au>Akiyama, Miki</au><au>Hagiwara, Akiko</au><au>Suzukamo, Yoshimi</au><au>Fukuhara, Shunichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan</atitle><jtitle>Health and quality of life outcomes</jtitle><addtitle>Health Qual Life Outcomes</addtitle><date>2006-08-18</date><risdate>2006</risdate><volume>4</volume><issue>1</issue><spage>52</spage><epage>52</epage><pages>52-52</pages><artnum>52</artnum><issn>1477-7525</issn><eissn>1477-7525</eissn><abstract>We constructed a concise multidimensional care burden scale that reflects circumstances unique to Japan, with a focus on intractable neurological diseases. We surveyed 646 family caregivers of patients with intractable neurological diseases or stroke using 28 preliminary care burden scale items obtained from qualitative research. The results were used to finalize the feeling of care burden scale (BIC: burden index of caregivers), and verify its reliability and validity.
The survey was conducted among caregivers providing home health care to patients with intractable neurological diseases (PD [Parkinson's disease], SCD [spinocerebellar degeneration], MSA [multiple system atrophy], and ALS [amyotrophic lateral sclerosis]) or CVA (cerebrovascular accident) using a mailed, self-administered questionnaire between November, 2003 and May, 2004.
Response rates for neurological and CVA caregivers were 50% and 67%, respectively, or 646 in total (PD, 279; SCD, 78; MSA, 39; ALS, 30; and CVA, 220). Item and exploratory factor analyses led to a reduction to 11 items, comprising 10 items from the 5 domains of time-dependent burden, emotional burden, existential burden, physical burden, and service-related burden; and 1 item on total burden. Examination of validity showed a moderate correlation between each domain of the BIC and the SF-8 (Health related quality of life scale, Short Form-8), while the correlation coefficient of the overall BIC and CES-D was 0.62. Correlation between the BIC and ZBI, a preexisting care burden scale, was high (r = 0.84), while that with the time spent on providing care was 0.47. The ICC (Intraclass correlation coefficient) by test-retest reliability was 0.83, and 0.68 to 0.80 by individual domain.
These results show that the BIC, a new care burden scale comprising 11 items, is highly reliable and valid.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>16919162</pmid><doi>10.1186/1477-7525-4-52</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Caregivers - psychology Cost of Illness Female Home Nursing - psychology Humans Japan Male Middle Aged Nervous System Diseases - classification Nervous System Diseases - nursing Psychometrics - instrumentation Quality of Life Spouses - psychology Stress, Psychological - diagnosis Stroke - nursing Surveys and Questionnaires |
title | Validation of the Burden Index of Caregivers (BIC), a multidimensional short care burden scale from Japan |
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