Integrating Caregiver Support into Multiple Sclerosis Care
With loss of mobility in Multiple Sclerosis (MS) comes increase in caregiver assistance, burden, stress, and depression. This 6-month feasibility study used a pre-post design to test integration of a validated, behavioral, caregiving intervention into an ongoing MS clinic. Because the program focuse...
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doaj-7f6abc945f044f20864e22acf193cebc2020-11-25T02:11:23ZengHindawi LimitedMultiple Sclerosis International2090-26542090-26622020-01-01202010.1155/2020/34367263436726Integrating Caregiver Support into Multiple Sclerosis CareJennifer Martindale-Adams0Jeffrey Zuber1Michael Levin2Robert Burns3Marshall Graney4Linda O. Nichols5Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USADepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USADepartment of Neurology, University of Tennessee Health Science Center, Memphis, TN, USAGeriatric Group of Memphis, Memphis, TN, USADepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USACaregiver Center, Veterans Affairs Medical Center, Departments of Preventive and Internal Medicine, University of Tennessee Health Science Center, Memphis, TN, USAWith loss of mobility in Multiple Sclerosis (MS) comes increase in caregiver assistance, burden, stress, and depression. This 6-month feasibility study used a pre-post design to test integration of a validated, behavioral, caregiving intervention into an ongoing MS clinic. Because the program focused on caregivers, there were no additional services provided to the persons living with MS other than usual medical care. Twenty-five MS caregivers received REACH VA (Resources for Enhancing All Caregivers’ Health in the VA), a six-session behavior-focused intervention during two to three months designed to increase caregiver skills in managing their own stress and burden and MS related issues and concerns, with a focus on mobility. Caregivers were assessed at baseline, three, and six months. Caregivers’ expectations of the program were to receive education on MS, caregiving and stress management skills, and support. The major benefits caregivers reported were understanding their loved one’s condition and how to better provide care. At six months, caregivers reported statistically and clinically significant improvements in depressive symptoms and bother with challenging MS behaviors. Persons with MS reported benefit for their caregivers and for themselves; 71% reported that their caregivers had helped them with mobility and function. Study results suggest that the addition of the brief REACH caregiver intervention into an MS clinic would benefit both caregivers and persons with MS. Although the intervention was six sessions over three months, benefit persisted at six months, suggesting durability of effects. This trial is registered with ClinicalTrials.gov NCT02835677.http://dx.doi.org/10.1155/2020/3436726 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jennifer Martindale-Adams Jeffrey Zuber Michael Levin Robert Burns Marshall Graney Linda O. Nichols |
spellingShingle |
Jennifer Martindale-Adams Jeffrey Zuber Michael Levin Robert Burns Marshall Graney Linda O. Nichols Integrating Caregiver Support into Multiple Sclerosis Care Multiple Sclerosis International |
author_facet |
Jennifer Martindale-Adams Jeffrey Zuber Michael Levin Robert Burns Marshall Graney Linda O. Nichols |
author_sort |
Jennifer Martindale-Adams |
title |
Integrating Caregiver Support into Multiple Sclerosis Care |
title_short |
Integrating Caregiver Support into Multiple Sclerosis Care |
title_full |
Integrating Caregiver Support into Multiple Sclerosis Care |
title_fullStr |
Integrating Caregiver Support into Multiple Sclerosis Care |
title_full_unstemmed |
Integrating Caregiver Support into Multiple Sclerosis Care |
title_sort |
integrating caregiver support into multiple sclerosis care |
publisher |
Hindawi Limited |
series |
Multiple Sclerosis International |
issn |
2090-2654 2090-2662 |
publishDate |
2020-01-01 |
description |
With loss of mobility in Multiple Sclerosis (MS) comes increase in caregiver assistance, burden, stress, and depression. This 6-month feasibility study used a pre-post design to test integration of a validated, behavioral, caregiving intervention into an ongoing MS clinic. Because the program focused on caregivers, there were no additional services provided to the persons living with MS other than usual medical care. Twenty-five MS caregivers received REACH VA (Resources for Enhancing All Caregivers’ Health in the VA), a six-session behavior-focused intervention during two to three months designed to increase caregiver skills in managing their own stress and burden and MS related issues and concerns, with a focus on mobility. Caregivers were assessed at baseline, three, and six months. Caregivers’ expectations of the program were to receive education on MS, caregiving and stress management skills, and support. The major benefits caregivers reported were understanding their loved one’s condition and how to better provide care. At six months, caregivers reported statistically and clinically significant improvements in depressive symptoms and bother with challenging MS behaviors. Persons with MS reported benefit for their caregivers and for themselves; 71% reported that their caregivers had helped them with mobility and function. Study results suggest that the addition of the brief REACH caregiver intervention into an MS clinic would benefit both caregivers and persons with MS. Although the intervention was six sessions over three months, benefit persisted at six months, suggesting durability of effects. This trial is registered with ClinicalTrials.gov NCT02835677. |
url |
http://dx.doi.org/10.1155/2020/3436726 |
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