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Caregivers' experiences of patients with moderate‐stage Alzheimer's disease: a qualitative study

Background Caregivers experience challenges in the longest stage of Alzheimer disease, the moderate stage, due to all day demanded caregiving, added with neuropsychiatric symptoms, and communication difficulties. Supporting challenges of caregiving is more effective when specific needs are assessed...

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Published in:Psychogeriatrics 2021-09, Vol.21 (5), p.763-772
Main Authors: Ozcan, Munevver, Akyar, İmatullah
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Language:English
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description Background Caregivers experience challenges in the longest stage of Alzheimer disease, the moderate stage, due to all day demanded caregiving, added with neuropsychiatric symptoms, and communication difficulties. Supporting challenges of caregiving is more effective when specific needs are assessed and real‐life experiences are appreciated. This study sought to explore caregivers' experiences and support needs for moderate‐stage Alzheimer's disease patients. Methods This study had a qualitative phenomenological design. In‐depth, semi‐structured interviews were conducted with 46 caregivers via face‐to‐face interviews. Following transcription, an analysis was done with Colaizzi's steps by coding and defining the main themes and subthemes. Results Caregivers stated they faced difficulties in the care activities of patients and needed support. Three themes were identified: (i) changes related to Alzheimer's disease; (ii) change in caregivers' life; and (iii) support needs and coping strategies about the care process. Conclusions Current study confirmed that caregivers of moderate‐stage Alzheimer's disease patients need proper support to cope with daily care activities and systems that help them overcome life challenges. The development of a system based on the stage‐specific caregivers' need to decrease daily care challenges and overwhelming economic and emotional stress can be recommended.
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Supporting challenges of caregiving is more effective when specific needs are assessed and real‐life experiences are appreciated. This study sought to explore caregivers' experiences and support needs for moderate‐stage Alzheimer's disease patients. Methods This study had a qualitative phenomenological design. In‐depth, semi‐structured interviews were conducted with 46 caregivers via face‐to‐face interviews. Following transcription, an analysis was done with Colaizzi's steps by coding and defining the main themes and subthemes. Results Caregivers stated they faced difficulties in the care activities of patients and needed support. Three themes were identified: (i) changes related to Alzheimer's disease; (ii) change in caregivers' life; and (iii) support needs and coping strategies about the care process. Conclusions Current study confirmed that caregivers of moderate‐stage Alzheimer's disease patients need proper support to cope with daily care activities and systems that help them overcome life challenges. The development of a system based on the stage‐specific caregivers' need to decrease daily care challenges and overwhelming economic and emotional stress can be recommended.</description><identifier>ISSN: 1346-3500</identifier><identifier>EISSN: 1479-8301</identifier><identifier>DOI: 10.1111/psyg.12736</identifier><language>eng</language><publisher>Melbourne: John Wiley &amp; Sons Australia, Ltd</publisher><subject>Alzheimer's disease ; care experience ; Caregivers ; Neural coding ; Neurodegenerative diseases ; Qualitative research ; supportive care ; Transcription</subject><ispartof>Psychogeriatrics, 2021-09, Vol.21 (5), p.763-772</ispartof><rights>2021 Japanese Psychogeriatric Society.</rights><rights>Psychogeriatrics © 2021 Japanese Psychogeriatric Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3586-f66c1049818efb125091585860c9513fd316fdc24ceab93cfd1fa7f011e4f3463</citedby><cites>FETCH-LOGICAL-c3586-f66c1049818efb125091585860c9513fd316fdc24ceab93cfd1fa7f011e4f3463</cites><orcidid>0000-0003-3551-8099</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Ozcan, Munevver</creatorcontrib><creatorcontrib>Akyar, İmatullah</creatorcontrib><title>Caregivers' experiences of patients with moderate‐stage Alzheimer's disease: a qualitative study</title><title>Psychogeriatrics</title><description>Background Caregivers experience challenges in the longest stage of Alzheimer disease, the moderate stage, due to all day demanded caregiving, added with neuropsychiatric symptoms, and communication difficulties. Supporting challenges of caregiving is more effective when specific needs are assessed and real‐life experiences are appreciated. This study sought to explore caregivers' experiences and support needs for moderate‐stage Alzheimer's disease patients. Methods This study had a qualitative phenomenological design. In‐depth, semi‐structured interviews were conducted with 46 caregivers via face‐to‐face interviews. Following transcription, an analysis was done with Colaizzi's steps by coding and defining the main themes and subthemes. Results Caregivers stated they faced difficulties in the care activities of patients and needed support. Three themes were identified: (i) changes related to Alzheimer's disease; (ii) change in caregivers' life; and (iii) support needs and coping strategies about the care process. Conclusions Current study confirmed that caregivers of moderate‐stage Alzheimer's disease patients need proper support to cope with daily care activities and systems that help them overcome life challenges. The development of a system based on the stage‐specific caregivers' need to decrease daily care challenges and overwhelming economic and emotional stress can be recommended.</description><subject>Alzheimer's disease</subject><subject>care experience</subject><subject>Caregivers</subject><subject>Neural coding</subject><subject>Neurodegenerative diseases</subject><subject>Qualitative research</subject><subject>supportive care</subject><subject>Transcription</subject><issn>1346-3500</issn><issn>1479-8301</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KxEAMx4souH5cfIIBD4pQnXTa2dabLH7BgoJ68FRmp5l1lnZbJ61aTz6Cz-iTOGs9eTCXJOT3D8k_CPaAH4OPk4b6-TFEYyHXghHE4yxMBYd1X4tYhiLhfDPYIlpwHsWJEKNgNlEO5_YFHR0wfGvQWVxqJFYb1qjWNy2xV9s-saou0KkWvz4-qVVzZGfl-xPaCt0BscISKsJTpthzp0rbeukLMmq7ot8JNowqCXd_83bwcHF-P7kKpzeX15OzaahFksrQSKmBx1kKKZoZRAnPIEn9hOssAWEKAdIUOoo1qlkmtCnAqLHhABgb_53YDg6HvY2rnzukNq8saSxLtcS6ozxKYik5TwA8uv8HXdSdW_rrPCVTkQkJqaeOBkq7msihyRtnK-X6HHi-sjtf2Z3_2O1hGOBXW2L_D5nf3j1eDppvXFOD0w</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Ozcan, Munevver</creator><creator>Akyar, İmatullah</creator><general>John Wiley &amp; Sons Australia, Ltd</general><general>Blackwell Publishing Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3551-8099</orcidid></search><sort><creationdate>202109</creationdate><title>Caregivers' experiences of patients with moderate‐stage Alzheimer's disease: a qualitative study</title><author>Ozcan, Munevver ; Akyar, İmatullah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3586-f66c1049818efb125091585860c9513fd316fdc24ceab93cfd1fa7f011e4f3463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alzheimer's disease</topic><topic>care experience</topic><topic>Caregivers</topic><topic>Neural coding</topic><topic>Neurodegenerative diseases</topic><topic>Qualitative research</topic><topic>supportive care</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ozcan, Munevver</creatorcontrib><creatorcontrib>Akyar, İmatullah</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Psychogeriatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ozcan, Munevver</au><au>Akyar, İmatullah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caregivers' experiences of patients with moderate‐stage Alzheimer's disease: a qualitative study</atitle><jtitle>Psychogeriatrics</jtitle><date>2021-09</date><risdate>2021</risdate><volume>21</volume><issue>5</issue><spage>763</spage><epage>772</epage><pages>763-772</pages><issn>1346-3500</issn><eissn>1479-8301</eissn><abstract>Background Caregivers experience challenges in the longest stage of Alzheimer disease, the moderate stage, due to all day demanded caregiving, added with neuropsychiatric symptoms, and communication difficulties. Supporting challenges of caregiving is more effective when specific needs are assessed and real‐life experiences are appreciated. This study sought to explore caregivers' experiences and support needs for moderate‐stage Alzheimer's disease patients. Methods This study had a qualitative phenomenological design. In‐depth, semi‐structured interviews were conducted with 46 caregivers via face‐to‐face interviews. Following transcription, an analysis was done with Colaizzi's steps by coding and defining the main themes and subthemes. Results Caregivers stated they faced difficulties in the care activities of patients and needed support. Three themes were identified: (i) changes related to Alzheimer's disease; (ii) change in caregivers' life; and (iii) support needs and coping strategies about the care process. 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subjects Alzheimer's disease
care experience
Caregivers
Neural coding
Neurodegenerative diseases
Qualitative research
supportive care
Transcription
title Caregivers' experiences of patients with moderate‐stage Alzheimer's disease: a qualitative study
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