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dc.contributor.advisorSusan Sullivan-Bolyai
dc.contributor.authorRaymond, Kathryn Y.
dc.date2022-08-11T08:09:03.000
dc.date.accessioned2022-08-23T16:16:41Z
dc.date.available2022-08-23T16:16:41Z
dc.date.issued2016-01-01
dc.date.submitted2016-04-04
dc.identifier.doi10.13028/scj0-b336
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34387
dc.description<p>Material from this dissertation has been published in: Raymond KY, Willis DG, Sullivan-Bolyai S. Parents Caring For Adult Children With Serious Mental Illness. J Am Psychiatr Nurses Assoc. 2017 Mar/Apr;23(2):119-132. doi: 10.1177/1078390316685404. Epub 2017 Jan 6. PubMed PMID: 28060601.</p>
dc.description.abstractThe purpose of this study was to examine parents’ management styles when caring for adult children with serious mental illness (SMI), as well as parents’ perspectives on what type of community-based mental health interventions would support and/or enhance overall family functioning. This qualitative descriptive study was undergirded by Knafl and Deatrick’s Family Management Style Framework. Thirty parents (N = 30) caring for adult children with SMI over age 18 were recruited as participants. Demographic data included age, gender, ethnicity, educational level, annual income, and National Alliance on Mental Illness membership. Parents were interviewed in their homes or other private setting. Verbal informed consent was obtained. Audio-recorded, individual, semistructured interviews were conducted until redundancy was achieved. Data were analyzed using qualitative content analysis. Four major themes emerged from the data. These themes described prolonged, difficult, and confusing phases that parents and the family undergo in caring for an adult child with SMI. These phases have a progressive nature, moving from parents recognizing that their child has a SMI to redefining family life as a result of caring for an adult child with SMI. Successful management of these phases must include increasing access to mental health information, mental health screening, early interventions, violence prevention, and various treatment options for adult children and their families.
dc.language.isoen_US
dc.relation<p><a href="https://escholarship.umassmed.edu/gsn_pp/56/" target="_blank">Published article based on this dissertation</a></p>
dc.rights© Copyright by Kathryn Y. Raymond 2016. All Rights Reserved.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectadult children
dc.subjectcaregiving
dc.subjectmanagement styles
dc.subjectparents
dc.subjectserious mental illness
dc.subjectMentally Ill Persons
dc.subjectFamily Relations
dc.subjectMental Disorders
dc.subjectParent-Child Relations
dc.subjectCommunity Health and Preventive Medicine
dc.subjectFamily, Life Course, and Society
dc.subjectMental and Social Health
dc.subjectMental Disorders
dc.subjectNursing
dc.titleParents Caring for Adult Children With Serious Mental Illness: A Qualitative Descriptive Study: A Dissertation
dc.typeDoctoral Dissertation
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1050&amp;context=gsn_diss&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsn_diss/40
dc.legacy.embargo2016-01-28T00:00:00-08:00
dc.identifier.contextkey8420950
refterms.dateFOA2022-08-24T03:50:41Z
html.description.abstract<p>The purpose of this study was to examine parents’ management styles when caring for adult children with serious mental illness (SMI), as well as parents’ perspectives on what type of community-based mental health interventions would support and/or enhance overall family functioning. This qualitative descriptive study was undergirded by Knafl and Deatrick’s Family Management Style Framework. Thirty parents (N = 30) caring for adult children with SMI over age 18 were recruited as participants. Demographic data included age, gender, ethnicity, educational level, annual income, and National Alliance on Mental Illness membership. Parents were interviewed in their homes or other private setting. Verbal informed consent was obtained. Audio-recorded, individual, semistructured interviews were conducted until redundancy was achieved. Data were analyzed using qualitative content analysis. Four major themes emerged from the data. These themes described prolonged, difficult, and confusing phases that parents and the family undergo in caring for an adult child with SMI. These phases have a progressive nature, moving from parents recognizing that their child has a SMI to redefining family life as a result of caring for an adult child with SMI. Successful management of these phases must include increasing access to mental health information, mental health screening, early interventions, violence prevention, and various treatment options for adult children and their families.</p>
dc.identifier.submissionpathgsn_diss/40
dc.contributor.departmentGraduate School of Nursing


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© Copyright by Kathryn Y. Raymond 2016. All Rights Reserved.
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