Abstract
Background: Review-based research is required to understand the spousal experiences and role transitions needed when care giving for patients with multiple sclerosis. The aim of the current study was to meet this need by undertaking a synthesis of qualitative research from the experiences of patients with MS.
Methods: A qualitative thematic synthesis was undertaken in 3 stages: (1) systematic search for literature, (2) critical appraisal of included studies and (3) synthesis of data using an a-priori framework.
Findings: A total of 10 studies with 120 spousal caregivers were included. Three major themes were identified: (1) motivation for care, (2) role transition and (3) relationship changes.
Conclusions: The findings present a variety of motivations amongst spousal caregivers, and report both positive and negative experiences of transition and relationship change. These findings have important implications for healthcare professionals, who work closely with caregivers in practice.
Methods: A qualitative thematic synthesis was undertaken in 3 stages: (1) systematic search for literature, (2) critical appraisal of included studies and (3) synthesis of data using an a-priori framework.
Findings: A total of 10 studies with 120 spousal caregivers were included. Three major themes were identified: (1) motivation for care, (2) role transition and (3) relationship changes.
Conclusions: The findings present a variety of motivations amongst spousal caregivers, and report both positive and negative experiences of transition and relationship change. These findings have important implications for healthcare professionals, who work closely with caregivers in practice.
| Original language | English |
|---|---|
| Pages (from-to) | 405-413 |
| Journal | International Journal of Therapy and Rehabilitation |
| Volume | 25 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 10 Aug 2018 |
Keywords
- Multiple Sclerosis
- caregiver
- Review
- Qualitative