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The life experience of leprosy families in maintaining interaction patterns in the family to support healing in leprosy patients in Indonesian society. A phenomenological qualitative study
Family involvement in overcoming the severity of leprosy is very important in the life of leprosy sufferers in communities who experience the clinical and, psychological, social and behavioral consequences of the disease. However, this need, psychosocial, is felt to be not optimal. This study is to...
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Published in: | PLoS neglected tropical diseases 2022-04, Vol.16 (4), p.e0010264-e0010264 |
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description | Family involvement in overcoming the severity of leprosy is very important in the life of leprosy sufferers in communities who experience the clinical and, psychological, social and behavioral consequences of the disease. However, this need, psychosocial, is felt to be not optimal. This study is to identify how the experiences of family members as caregivers provide assistance to lepers in improving healing and maintaining patterns of interaction in the family.
The design uses qualitative research with in-depth, face-to-face interviews with family members in a semi-structured manner with the hope of obtaining complete data. Using purposive sampling with Participatory Interpretative Phenomenology analysis, there are 12 families with 15 family members consisting of 4 men and 11 women.
This study produced a family theme that tried to follow what would happen to lepers, with four sub-categories: 1) Using various coping alternatives to recognize the disease, 2) Family members in the shadow of leprosy, 3) Trying to empathize with other family members. sick, 4) Caring for the emotional response of the family and seeking support.
This analysis shows that deficiency in cognitive aspects can be closed by maintaining a lifestyle in the family through efforts to understand, support, establish communication, increase maximum involvement in restoring self-confidence, especially in lepers with psychosocial problems in the family. The results of this study can be used as psychosocial support in maintaining communication between family members to support treatment programs and accelerate the recovery of leprosy. |
doi_str_mv | 10.1371/journal.pntd.0010264 |
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The design uses qualitative research with in-depth, face-to-face interviews with family members in a semi-structured manner with the hope of obtaining complete data. Using purposive sampling with Participatory Interpretative Phenomenology analysis, there are 12 families with 15 family members consisting of 4 men and 11 women.
This study produced a family theme that tried to follow what would happen to lepers, with four sub-categories: 1) Using various coping alternatives to recognize the disease, 2) Family members in the shadow of leprosy, 3) Trying to empathize with other family members. sick, 4) Caring for the emotional response of the family and seeking support.
This analysis shows that deficiency in cognitive aspects can be closed by maintaining a lifestyle in the family through efforts to understand, support, establish communication, increase maximum involvement in restoring self-confidence, especially in lepers with psychosocial problems in the family. The results of this study can be used as psychosocial support in maintaining communication between family members to support treatment programs and accelerate the recovery of leprosy.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0010264</identifier><identifier>PMID: 35394998</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Biology and Life Sciences ; Care and treatment ; Caregivers - psychology ; Cognitive ability ; Communication ; Data collection ; Diagnosis ; Disease transmission ; Domestic relations ; Families & family life ; Family - psychology ; Female ; Healing ; Health aspects ; Humans ; Indonesia ; Interviews ; Leprosy ; Leprosy - psychology ; Life Change Events ; Male ; Medicine and Health Sciences ; Men ; Methods ; Nursing ; People and Places ; Phenomenology ; Prevention ; Psychological aspects ; Qualitative Research ; Research and Analysis Methods ; Researchers ; Risk factors ; Social networks ; Social Sciences ; Stigma ; Tropical diseases ; Women</subject><ispartof>PLoS neglected tropical diseases, 2022-04, Vol.16 (4), p.e0010264-e0010264</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Nasir et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Nasir et al 2022 Nasir et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c624t-281fcc2c849037874cdde5ff30da0b3b900c1a5abe507d1cc9b01dca9b006d103</citedby><cites>FETCH-LOGICAL-c624t-281fcc2c849037874cdde5ff30da0b3b900c1a5abe507d1cc9b01dca9b006d103</cites><orcidid>0000-0002-6669-0767 ; 0000-0003-2086-2735</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2665135938/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2665135938?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35394998$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Penna, Gerson Oliveira</contributor><creatorcontrib>Nasir, Abd</creatorcontrib><creatorcontrib>Yusuf, Ah</creatorcontrib><creatorcontrib>Listiawan, Muhammad Yulianto</creatorcontrib><creatorcontrib>Makhfudli, Makhfudli</creatorcontrib><title>The life experience of leprosy families in maintaining interaction patterns in the family to support healing in leprosy patients in Indonesian society. A phenomenological qualitative study</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Family involvement in overcoming the severity of leprosy is very important in the life of leprosy sufferers in communities who experience the clinical and, psychological, social and behavioral consequences of the disease. However, this need, psychosocial, is felt to be not optimal. This study is to identify how the experiences of family members as caregivers provide assistance to lepers in improving healing and maintaining patterns of interaction in the family.
The design uses qualitative research with in-depth, face-to-face interviews with family members in a semi-structured manner with the hope of obtaining complete data. Using purposive sampling with Participatory Interpretative Phenomenology analysis, there are 12 families with 15 family members consisting of 4 men and 11 women.
This study produced a family theme that tried to follow what would happen to lepers, with four sub-categories: 1) Using various coping alternatives to recognize the disease, 2) Family members in the shadow of leprosy, 3) Trying to empathize with other family members. sick, 4) Caring for the emotional response of the family and seeking support.
This analysis shows that deficiency in cognitive aspects can be closed by maintaining a lifestyle in the family through efforts to understand, support, establish communication, increase maximum involvement in restoring self-confidence, especially in lepers with psychosocial problems in the family. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nasir, Abd</au><au>Yusuf, Ah</au><au>Listiawan, Muhammad Yulianto</au><au>Makhfudli, Makhfudli</au><au>Penna, Gerson Oliveira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The life experience of leprosy families in maintaining interaction patterns in the family to support healing in leprosy patients in Indonesian society. A phenomenological qualitative study</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>16</volume><issue>4</issue><spage>e0010264</spage><epage>e0010264</epage><pages>e0010264-e0010264</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>Family involvement in overcoming the severity of leprosy is very important in the life of leprosy sufferers in communities who experience the clinical and, psychological, social and behavioral consequences of the disease. However, this need, psychosocial, is felt to be not optimal. This study is to identify how the experiences of family members as caregivers provide assistance to lepers in improving healing and maintaining patterns of interaction in the family.
The design uses qualitative research with in-depth, face-to-face interviews with family members in a semi-structured manner with the hope of obtaining complete data. Using purposive sampling with Participatory Interpretative Phenomenology analysis, there are 12 families with 15 family members consisting of 4 men and 11 women.
This study produced a family theme that tried to follow what would happen to lepers, with four sub-categories: 1) Using various coping alternatives to recognize the disease, 2) Family members in the shadow of leprosy, 3) Trying to empathize with other family members. sick, 4) Caring for the emotional response of the family and seeking support.
This analysis shows that deficiency in cognitive aspects can be closed by maintaining a lifestyle in the family through efforts to understand, support, establish communication, increase maximum involvement in restoring self-confidence, especially in lepers with psychosocial problems in the family. The results of this study can be used as psychosocial support in maintaining communication between family members to support treatment programs and accelerate the recovery of leprosy.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>35394998</pmid><doi>10.1371/journal.pntd.0010264</doi><orcidid>https://orcid.org/0000-0002-6669-0767</orcidid><orcidid>https://orcid.org/0000-0003-2086-2735</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biology and Life Sciences Care and treatment Caregivers - psychology Cognitive ability Communication Data collection Diagnosis Disease transmission Domestic relations Families & family life Family - psychology Female Healing Health aspects Humans Indonesia Interviews Leprosy Leprosy - psychology Life Change Events Male Medicine and Health Sciences Men Methods Nursing People and Places Phenomenology Prevention Psychological aspects Qualitative Research Research and Analysis Methods Researchers Risk factors Social networks Social Sciences Stigma Tropical diseases Women |
title | The life experience of leprosy families in maintaining interaction patterns in the family to support healing in leprosy patients in Indonesian society. A phenomenological qualitative study |
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