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Faculty of Graduate Studies and Research, University of Regina

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

Abstract

dc:description.abstract

Cystic 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.

Degree

thesis:*
Name thesis:degree_name
Master of Arts (MA)
Level thesis:degree_level
Master's
Discipline thesis:degree_discipline
Clinical Psychology
Grantor dc:publisher
Faculty of Graduate Studies and Research, University of Regina
Year dc:date.issued
2020

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Shivak, Shelby Marie
Advisor dc:contributor.advisor
  • Wright, Kristi
Committee members dc:contributor.committeemember
  • Gordon, Jennifer
  • Loucks, Jeff
  • Genoe, Rebecca

Rights

Language dc:language.iso
en

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:uregina.scholaris.ca:10294/9332

Chain of custody

source
Harvested from
University of Regina
Base URL
uregina.scholaris.ca/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Shivak, Shelby Marie. A Qualitative Exploration of the Information and Service Needs of Youth Siblings of Individuals with Cystic Fibrosis. Master's thesis, Faculty of Graduate Studies and Research, University of Regina, 2020. https://hdl.handle.net/10294/9332