Literature DB >> 9783879

Spousal caregivers' activity restriction and depression: a model for changes over time.

A P Nieboer1, R Schulz, K A Matthews, M F Scheier, J Ormel, S M Lindenberg.   

Abstract

In this paper we examine the effects of increasing as well as decreasing caregiving demands on depressive symptomatology. In addition, we focus on spousal caregivers' activity restriction as an explanatory mechanism for changes in depressive symptomatology in the caregiving context. Two databases are used to answer our research questions. An increase of caregiving demands is assessed in study 1, which includes prospective data on 127 spousal caregivers of stroke, hip fracture, congestive heart failure and myocardial infarction patients. A decrease of caregiving demands is examined in study 2, which includes prospective data on 110 spousal caregivers of bypass operation patients. The results generally support the hypothesis that an increase in caregiving demands results in increased depressive symptomatology, while a decrease in caregiving demands reduces depressive symptomatology. The results also support the notion of activity restriction as a critical mediator of changes in depressive symptoms. Cross-sectionally it mediates the association between caregiving and depressive symptomatology, and longitudinally it contributes to changes in depressive symptomatology in both samples.

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Year:  1998        PMID: 9783879     DOI: 10.1016/s0277-9536(98)00214-7

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  28 in total

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2.  Activity Restriction and Depressive Symptoms in Older Couples.

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Journal:  J Aging Health       Date:  2016-07-19

Review 3.  Physical and mental health effects of family caregiving.

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4.  Depression and quality of informal care: a longitudinal investigation of caregiving stressors.

Authors:  G Rush Smith; Gail M Williamson; L Stephen Miller; Richard Schulz
Journal:  Psychol Aging       Date:  2011-09

5.  Activity restriction and depression in medical patients and their caregivers: a meta-analysis.

Authors:  Brent T Mausbach; Elizabeth A Chattillion; Raeanne C Moore; Susan K Roepke; Colin A Depp; Scott Roesch
Journal:  Clin Psychol Rev       Date:  2011-04-28

6.  How is an informal caregiver's psychological distress associated with prolonged caregiving? Evidence from a six-wave panel survey in Japan.

Authors:  Takashi Oshio
Journal:  Qual Life Res       Date:  2015-06-07       Impact factor: 4.147

7.  Effects of home, outside leisure, social, and peer activity on psychological health among Japanese family caregivers.

Authors:  Tomoko Wakui; Tami Saito; Emily M Agree; Ichiro Kai
Journal:  Aging Ment Health       Date:  2012-02-24       Impact factor: 3.658

8.  Predictors and consequences of perceived lack of choice in becoming an informal caregiver.

Authors:  Richard Schulz; Scott R Beach; Thomas B Cook; Lynn M Martire; Jennifer M Tomlinson; Joan K Monin
Journal:  Aging Ment Health       Date:  2012-02-24       Impact factor: 3.658

9.  A dyadic model of living with epilepsy based on the perspectives of adults with epilepsy and their support persons.

Authors:  Elizabeth Reisinger Walker; Christina Barmon; Robin E McGee; George Engelhard; Claire E Sterk; Colleen DiIorio; Nancy J Thompson
Journal:  Epilepsy Behav       Date:  2015-10-24       Impact factor: 2.937

10.  Widowhood and depression among older Europeans--the role of gender, caregiving, marital quality, and regional context.

Authors:  Barbara Schaan
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2013-05       Impact factor: 4.077

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