A Qualitative Exploration of the Information and Service Needs of Youth Siblings of Individuals with Cystic Fibrosis

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dc.contributor.advisorWright, Kristi
dc.contributor.authorShivak, Shelby Marie
dc.contributor.committeememberGordon, Jennifer
dc.contributor.committeememberLoucks, Jeff
dc.contributor.committeememberGenoe, Rebecca
dc.contributor.externalexaminerMatthews, Elise
dc.date.accessioned2020-12-13T16:25:06Z
dc.date.available2020-12-13T16:25:06Z
dc.date.issued2020-06
dc.descriptionA Thesis Submitted to the Faculty of Graduate Studies and Research In Partial Fulfillment of the Requirements for the Degree of Master of Arts in Clinical Psychology, University of Regina. X, 167 p.en_US
dc.description.abstractCystic Fibrosis (CF) is a progressive, fatal inherited disease common amongst Caucasian children and young adults in Canada. In addition to being one of the most difficult chronic health conditions to manage, siblings of children and adolescents with CF have been shown to experience elevated psychological symptoms (e.g., depression and anxiety), negative social adjustment, and internalizing behaviours. While the need to address these concerns by providing appropriate information and services is evident, to date there are no tailored mental health programs designed for siblings of children and adolescents with CF. There were five main objectives for the present research: To explore (1) what challenges healthy siblings of youth with CF face, (2) what information about CF healthy siblings of youth with CF need, (3) what types of mental health services healthy siblings of youth with CF need, (4) the perceived benefits and/or drawbacks of obtaining services via the Internet, and (5) what components should be included in an interactive, Internet-delivered mental health prevention program for healthy siblings of youth with CF. Participants (n = 10) included four youth siblings of pa Mage = 36.67, SD = rent caregivers ( a six nd w Mage = 10.25, SD = 2.77) ith CF ( yout h 3.40) recruited from CF clinics and chapters in Saskatchewan, Canada. Siblings and parent caregivers completed brief demographic questionnaires and participated in individual semi-structured interviews. Thematic content analysis was used to analyze the data collected from each participant group with reference to the main study objectives. Sibling participant responses uncovered four major themes: (1) life balance, (2) emotional challenges, (3) coping, and (4) bridging gaps in sibling care. Parent responses uncovered six major themes: (1) life balance, (2) emotional challenges, (3) coping, (4) developing and maintaining relationships, (5) education, and (6) improving mental health services. The results of the present study highlight the unique challenges experienced by siblings and families of youth with CF and the need for effective family support in coping with CF. Information obtained from the study will be used to inform the development of an evidence-based, Internet-delivered mental health program aimed at improving the overall mental health functioning and quality of life of this population.en_US
dc.description.authorstatusStudenten
dc.description.peerreviewyesen
dc.identifier.tcnumberTC-SRU-9332
dc.identifier.thesisurlhttps://ourspace.uregina.ca/bitstream/handle/10294/9332/Shivak_Shelby_MA_ClinPSYC_Fall2020.pdf
dc.identifier.urihttps://hdl.handle.net/10294/9332
dc.language.isoenen_US
dc.publisherFaculty of Graduate Studies and Research, University of Reginaen_US
dc.titleA Qualitative Exploration of the Information and Service Needs of Youth Siblings of Individuals with Cystic Fibrosisen_US
dc.typeThesisen_US
thesis.degree.departmentDepartment of Psychologyen_US
thesis.degree.disciplineClinical Psychologyen_US
thesis.degree.grantorUniversity of Reginaen
thesis.degree.levelMaster'sen
thesis.degree.nameMaster of Arts (MA)en_US
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