Informing the Development of an Internet-delivered Mental Health Program for Youth with Cystic Fibrosis: A Qualitative Study

dc.contributor.advisorWright, Kristi
dc.contributor.authorPower, Hilary Ann
dc.contributor.committeememberKlest, Bridget
dc.contributor.committeememberLoucks, Jeff
dc.contributor.committeememberGenoe, Rebecca
dc.contributor.externalexaminerUrban, Ann-Marie
dc.date.accessioned2020-08-29T00:19:56Z
dc.date.available2020-08-29T00:19:56Z
dc.date.issued2019-09
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. xiii, 247 p.en_US
dc.description.abstractYouth with cystic fibrosis (CF) and their parent caregivers have been shown to experience elevated psychological symptoms. The need to address these issues through providing appropriate information and services to this population is evident. At present, there is no specific mental health program designed for youth with CF in Canada. The current study qualitatively examined the information and service needs of youth with CF. Participants (n = 16) included five youth with CF (Mage = 9.40, SD = 1.01), seven parent caregivers (Mage = 36.43, SD = 3.46), and four CF health care professionals (Mage = 44.00, SD = 10.46) recruited from CF clinics and chapters in Saskatchewan, Canada. Participants completed a brief demographic questionnaire. Semi-structured individual interviews were conducted with all participants. Thematic content analysis was used to analyze the data collected for each participant group. Four major themes were uncovered from youth participant responses: (1) challenges living with CF, (2) building independence, (3) coping, (4) bridging gaps in services. Six major themes were uncovered from parent participant responses: (1) emotional challenges (2) social challenges, (3) demanding treatments, (4) coping, (5) encouraging independence, and (6) improving services. Six major themes were uncovered from health care professional participant responses: (1) emotional challenges, (2) social challenges, (3) lifestyle restrictions, (4) developing independence, (5) barriers to care and managing CF, and (6) focusing on future mental health care. The findings highlight the many challenges experienced by youth with CF and their families. The results also draw attention to the importance of providing effective support in managing and coping with CF. Information gathered in the present study will be later used, in combination with the empirical literature, to inform the development of an evidence-based, Internet-delivered mental health program for this population.Keywords: Cystic fibrosis, psychopathology, children, adolescents, Internet intervention, mental health, qualitative designen_US
dc.description.authorstatusStudenten
dc.description.peerreviewyesen
dc.identifier.tcnumberTC-SRU-9227
dc.identifier.thesisurlhttps://ourspace.uregina.ca/bitstream/handle/10294/9227/Power_Hilary_MA_CP_Spring2020.pdf
dc.identifier.urihttps://hdl.handle.net/10294/9227
dc.language.isoenen_US
dc.publisherFaculty of Graduate Studies and Research, University of Reginaen_US
dc.titleInforming the Development of an Internet-delivered Mental Health Program for Youth with Cystic Fibrosis: A Qualitative Studyen_US
dc.typeThesisen
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
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Power_Hilary_MA_CP_Spring2020.pdf
Size:
5.31 MB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
2.22 KB
Format:
Item-specific license agreed upon to submission
Description:
Collections