TY - JOUR
T1 - Understanding the health impact of caregiving
T2 - A qualitative study of immigrant parents and single parents of children with cancer
AU - Klassen, Anne F.
AU - Gulati, Sonia
AU - Granek, Leeat
AU - Rosenberg-Yunger, Zahava R.S.
AU - Watt, Lisa
AU - Sung, Lillian
AU - Klaassen, Robert
AU - Dix, David
AU - Shaw, Nicola T.
N1 - Funding Information:
Acknowledgments This research was conducted with support from C17 and funded by Childhood Cancer Canada Foundation and the Canadian Cancer Society (grant #18043 and grant #020398). Anne Klassen is a recipient of a CIHR career award.
PY - 2012/11/1
Y1 - 2012/11/1
N2 - Purpose Research looking at the health of parents of children with cancer typically uses outcome measures focused on symptoms of anxiety, depression, or posttraumatic stress. Our team builds on this literature to provide a more comprehensive understanding of the health impact of caregiving. Methods Interviews were conducted with 79 Canadian parents of children with cancer at least 6 months postdiagnosis. Line-by-line coding was used to establish categories and themes. Constant comparison was used to examine relationships within and across codes and categories. Interviewing continued until no new themes emerged. Results Parents described health concerns as including sleep disturbance, daytime fatigue, anxiety, depression, social isolation, and changes in social roles. Parents described the positive impacts of caregiving as including gaining a greater appreciation for child and family and developing compassion, empathy, patience, inner strength, and new perspectives on life. Conclusion Parents of children with cancer can experience a range of health problems due to the emotional impact of a cancer diagnosis and the intensive and often prolonged nature of treatment and aftercare. Given the central role parents play as caregivers, it is crucial to understand the health impact of caregiving so that supportive interventions can be implemented as necessary.
AB - Purpose Research looking at the health of parents of children with cancer typically uses outcome measures focused on symptoms of anxiety, depression, or posttraumatic stress. Our team builds on this literature to provide a more comprehensive understanding of the health impact of caregiving. Methods Interviews were conducted with 79 Canadian parents of children with cancer at least 6 months postdiagnosis. Line-by-line coding was used to establish categories and themes. Constant comparison was used to examine relationships within and across codes and categories. Interviewing continued until no new themes emerged. Results Parents described health concerns as including sleep disturbance, daytime fatigue, anxiety, depression, social isolation, and changes in social roles. Parents described the positive impacts of caregiving as including gaining a greater appreciation for child and family and developing compassion, empathy, patience, inner strength, and new perspectives on life. Conclusion Parents of children with cancer can experience a range of health problems due to the emotional impact of a cancer diagnosis and the intensive and often prolonged nature of treatment and aftercare. Given the central role parents play as caregivers, it is crucial to understand the health impact of caregiving so that supportive interventions can be implemented as necessary.
KW - Caregivers
KW - Neoplasms
KW - Parents
KW - Qualitative research
KW - Quality of life
UR - http://www.scopus.com/inward/record.url?scp=84867985173&partnerID=8YFLogxK
U2 - 10.1007/s11136-011-0072-8
DO - 10.1007/s11136-011-0072-8
M3 - Article
AN - SCOPUS:84867985173
SN - 0962-9343
VL - 21
SP - 1595
EP - 1605
JO - Quality of Life Research
JF - Quality of Life Research
IS - 9
ER -