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Positive and negative experiences of caregivers helping power wheelchair users: a mixed-method study.
Labbé, Delphine; Yao, Daryl G; Miller, William C; Routhier, François; Rushton, Paula W; Demers, Louise; Mortenson, W Ben.
Afiliação
  • Labbé D; Department of Occupational Science and Occupational Therapy, University of British Columbia, Vancouver, British Columbia, Canada.
  • Yao DG; Rehabilitation Research Lab, Vancouver, British Columbia, Canada.
  • Miller WC; Department of Disability and Human Development, University of Illinois at Chicago, Chicago, Illinois, USA.
  • Routhier F; Department of Occupational Science and Occupational Therapy, University of British Columbia, Vancouver, British Columbia, Canada.
  • Rushton PW; Rehabilitation Research Lab, Vancouver, British Columbia, Canada.
  • Demers L; ICORD Research Center, Vancouver, British Columbia, Canada.
  • Mortenson WB; Department of Rehabilitation, Université Laval, Québec, Québec, Canada.
Disabil Rehabil Assist Technol ; : 1-12, 2024 Feb 11.
Article em En | MEDLINE | ID: mdl-38341650
ABSTRACT

PURPOSE:

This study aimed to better understand how the powered wheelchair (PWC) impacts the experiences of family caregivers of PWC users, and explore the strategies and resources used by caregivers to cope with their role. MATERIALS AND

METHODS:

This mixed-methods study was part of a larger cross-sectional research study conducted in four Canadian cities. Twenty-three family caregivers of PWC users, who provided at least 2 h of support per week, completed the Power Mobility Caregiver Assistive Technology Outcome (PM-CATOM), an 18-item measure assessing PWC-related and overall burden experienced by family caregivers. We also conducted semi-structured interviews and analysed them using inductive content analysis.

RESULTS:

From the quantitative PM-CATOM results, the caregivers perceived low level of burden for the wheelchair-related items, (Median4.5; Range 3 to 5). Most perceived burden when physically helping the wheelchair user and when providing verbal hints. In terms of overall help, the caregivers experienced some level of burden (Median 3.5 Range 3 to 5). Most caregivers identified burden associated with the limitation to their recreational and/or leisure activities (52.2%) and feeling that they have more to do than they can handle. We identified 3 themes in the interviews the burden experiences of caring for PWC users, the positive experiences of caregiving, and the coping strategies and resources used by caregivers of PWC users.

CONCLUSION:

Our study showed that understanding the experiences of caregivers of AT users is central as they are directly and indirectly impacted by the PWC in their lives and caregiving roles.
The caregivers experienced some burden related to wheelchair-related help, especially around the driving of the powered wheelchair (PWC).However, the PWC provide independence not only to the user but also to the family caregivers, allowing them to share quality time and helping each otherThe PWC impact the interaction with the social and physical environment of the caregivers.Caregiver-oriented interventions should build on the strengths of the caregivers and contribute to their well-being.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Qualitative_research Idioma: En Revista: Disabil Rehabil Assist Technol Assunto da revista: REABILITACAO Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Qualitative_research Idioma: En Revista: Disabil Rehabil Assist Technol Assunto da revista: REABILITACAO Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá