Caregiver burden, time spent caring and health status in the first 12 months following stroke.

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Title: Caregiver burden, time spent caring and health status in the first 12 months following stroke.
Authors: Tooth, L. (AUTHOR), Mckenna, K. (AUTHOR), Barnett, A. (AUTHOR), Prescott, C. (AUTHOR), Murphy, S. (AUTHOR)
Source: Brain Injury. Nov2005, Vol. 19 Issue 12, p963-974. 12p. 1 Diagram, 7 Charts.
Subjects: Caregivers, Mental health, Cerebrovascular disease, Medical rehabilitation, Cognition, Motor ability
Abstract: Objective : To quantify time caring, burden and health status in carers of stroke patients after discharge from rehabilitation; to identify the potentially modifiable sociodemographic and clinical characteristics associated with these outcomes. Methods : Patients and carers prospectively interviewed 6 ( n   =  71) and 12 ( n   =  57) months after discharge. Relationships of carer and patient variables with burden, health status and time analysed by Gaussian and Poisson regression. Results : Carers showed considerable burden at 6 and 12 months. Carers spent 4.6 and 3.6 hours per day assisting patients with daily activities at 6 and 12 months, respectively. Improved patient motor and cognitive function were associated with reductions of up to 20 minutes per day in time spent in daily activities. Better patient mental health and cognitive function were associated with better carer mental health. Conclusions : Potentially modifiable factors such as these may be able to be targeted by caregiver training, support and education programmes and outpatient therapy for patients. [ABSTRACT FROM AUTHOR]
Copyright of Brain Injury is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Psychology and Behavioral Sciences Collection
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  Data: Caregiver burden, time spent caring and health status in the first 12 months following stroke.
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  Data: <searchLink fieldCode="AR" term="%22Tooth%2C+L%2E%22">Tooth, L.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mckenna%2C+K%2E%22">Mckenna, K.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Barnett%2C+A%2E%22">Barnett, A.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Prescott%2C+C%2E%22">Prescott, C.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Murphy%2C+S%2E%22">Murphy, S.</searchLink> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Brain+Injury%22">Brain Injury</searchLink>. Nov2005, Vol. 19 Issue 12, p963-974. 12p. 1 Diagram, 7 Charts.
– Name: Subject
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  Data: <searchLink fieldCode="DE" term="%22Caregivers%22">Caregivers</searchLink><br /><searchLink fieldCode="DE" term="%22Mental+health%22">Mental health</searchLink><br /><searchLink fieldCode="DE" term="%22Cerebrovascular+disease%22">Cerebrovascular disease</searchLink><br /><searchLink fieldCode="DE" term="%22Medical+rehabilitation%22">Medical rehabilitation</searchLink><br /><searchLink fieldCode="DE" term="%22Cognition%22">Cognition</searchLink><br /><searchLink fieldCode="DE" term="%22Motor+ability%22">Motor ability</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Objective : To quantify time caring, burden and health status in carers of stroke patients after discharge from rehabilitation; to identify the potentially modifiable sociodemographic and clinical characteristics associated with these outcomes. Methods : Patients and carers prospectively interviewed 6 ( n   =  71) and 12 ( n   =  57) months after discharge. Relationships of carer and patient variables with burden, health status and time analysed by Gaussian and Poisson regression. Results : Carers showed considerable burden at 6 and 12 months. Carers spent 4.6 and 3.6 hours per day assisting patients with daily activities at 6 and 12 months, respectively. Improved patient motor and cognitive function were associated with reductions of up to 20 minutes per day in time spent in daily activities. Better patient mental health and cognitive function were associated with better carer mental health. Conclusions : Potentially modifiable factors such as these may be able to be targeted by caregiver training, support and education programmes and outpatient therapy for patients. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Brain Injury is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – Type: doi
        Value: 10.1080/02699050500110785
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      – Code: eng
        Text: English
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        PageCount: 12
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      – SubjectFull: Caregivers
        Type: general
      – SubjectFull: Mental health
        Type: general
      – SubjectFull: Cerebrovascular disease
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      – SubjectFull: Medical rehabilitation
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      – SubjectFull: Cognition
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      – SubjectFull: Motor ability
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              M: 11
              Text: Nov2005
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              Y: 2005
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