A Qualitative Study of Caregiving for Adolescents and Young Adults With Spinal Cord Injuries: Lessons From Lived Experiences

被引:5
作者
Haywood, Carol [1 ]
Pyatak, Elizabeth [2 ]
Leland, Natalie [3 ]
Henwood, Benjamin [4 ]
Lawlor, Mary C. [2 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, 633 N St Clair St,20th Floor, Chicago, IL 60611 USA
[2] Univ Southern Calif, Mrs TH Chan Div Occupat Sci & Occupat Therapy, Los Angeles, CA 90007 USA
[3] Univ Pittsburgh, Dept Occupat Therapy, Sch Hlth & Rehabil Sci, Pittsburgh, PA USA
[4] Univ Southern Calif, Suzanne Dworak Peck Sch Social Work, Los Angeles, CA 90007 USA
关键词
adolescence; caregiving; qualitative; spinal cord injury; young adulthood; FAMILY CAREGIVERS; HEALTH; CHILDREN; CHALLENGES; YOUTH; NEEDS; MODEL; RISK; CARE;
D O I
10.1310/sci2504-281
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective: To examine characteristics of caregiving from the perspectives of adolescents and young adults (AYAs) with spinal cord injuries (SCIs) and their informal caregivers to address outstanding gaps in knowledge relating to definitions of caregiving and its associated practices for this population. Methods: A multiphase qualitative design was applied, using phenomenological and narrative methods to capture data in participants' homes and communities. Participants were recruited from rehabilitation hospitals and community organizations throughout Los Angeles County, California. Inclusion criteria for AYAs included being 15-22 years old, having acquired an SCI within the previous 5 years, and using a wheelchair for mobility. The AYAs nominated persons they identified as primary caregivers to also participate. Data were collected through individual and group interviews as well as activity observations. Results: Data from the 17 participants (9 AYAs and 8 informal, primary caregivers) revealed ways in which the meaning of caregiving varied among dyads. Caregiving practices extended beyond physical assistance to include support for a range of day-to-day activities spanning from practical needs to facilitating developmental trajectories. Although AYAs expressed ideas about preferred caregiver characteristics, care partnerships appeared to be guided more by availability than preference. Conclusion: Phenomenological analysis revealed that the meaning of "caregiving" and its associated practices are highly individualized for AYAs with SCIs. Caregiving is rooted in personal needs related to effects of SCI and developmental goals. Everyday practices are shaped by individual relationships and the beliefs of AYAs and their caregivers. Addressing influences of caregiving on long-term health and function may require attention to developmental processes, caregiver "fit," and ways care is, or can be, distributed throughout broader networks according to personal needs and preferences.
引用
收藏
页码:281 / 289
页数:9
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