Literature DB >> 16273992

Subjective appraisal of Alzheimer's disease caregiving: the role of self-efficacy and depressive symptoms in the experience of burden.

Judith G Gonyea1, Maureen O'Connor, Anastasia Carruth, Patricia A Boyle.   

Abstract

Most studies investigating correlates of Alzheimer's disease (AD) caregiver burden have focused on the role of objective factors as opposed to subjective factors. Although objective variables (e.g., caregiver age, patient dementia severity, functional status) have been shown to be significantly associated with burden, the correlations generally are modest and explain relatively little of the variability in caregiver outcomes. Moreover, many of these objective variables are not modifiable and are of limited use in the development of caregiver interventions. Thus, there continues to be a need to identify powerful and modifiable determinants of caregiver burden. This study examined the role of two subjective factors-self-efficacy and depressive symptoms-as predictors of AD caregiver burden. Based on a sample of 80 AD caregivers, hierarchical regression analyses revealed that self-efficacy and depressive symptoms each had a significant independent effect on the experience of burden even after accounting for objective factors. These findings suggest that caregiver interventions aimed to reduce burden may benefit from the incorporation of specific strategies to increase self-efficacy and decrease depressive symptoms.

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Year:  2005        PMID: 16273992     DOI: 10.1177/153331750502000505

Source DB:  PubMed          Journal:  Am J Alzheimers Dis Other Demen        ISSN: 1533-3175            Impact factor:   2.035


  15 in total

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4.  Unmet needs of caregivers of individuals referred to a dementia care program.

Authors:  Lee A Jennings; David B Reuben; Leslie Chang Evertson; Katherine S Serrano; Linda Ercoli; Joshua Grill; Joshua Chodosh; Zaldy Tan; Neil S Wenger
Journal:  J Am Geriatr Soc       Date:  2015-02       Impact factor: 5.562

5.  Gender differences in caregiving among family - caregivers of people with mental illnesses.

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Journal:  World J Psychiatry       Date:  2016-03-22

6.  Theory-guided selection of discrimination measures for racial/ ethnic health disparities research among older adults.

Authors:  Angela D Thrasher; Olivio J Clay; Chandra L Ford; Anita L Stewart
Journal:  J Aging Health       Date:  2012-03-26

7.  CareHeroes Web and Android™ Apps for Dementia Caregivers: A Feasibility Study.

Authors:  Ellen Leslie Brown; Nicole Ruggiano; Timothy F Page; Lisa Roberts; Vagelis Hristidis; Karen L Whiteman; Joana Castro
Journal:  Res Gerontol Nurs       Date:  2016-03-04       Impact factor: 1.571

8.  How much striving is too much? John Henryism active coping predicts worse daily cortisol responses for African American but not white female dementia family caregivers.

Authors:  Marcellus M Merritt; T J McCallum; Thomas Fritsch
Journal:  Am J Geriatr Psychiatry       Date:  2011-05       Impact factor: 4.105

9.  Perceived stress and depressive symptoms not neuropsychiatric symptoms predict caregiver burden in Alzheimer's disease: a cross-sectional study.

Authors:  Manee Pinyopornpanish; Kanokporn Pinyopornpanish; Atiwat Soontornpun; Surat Tanprawate; Angkana Nadsasarn; Nahathai Wongpakaran; Tinakon Wongpakaran
Journal:  BMC Geriatr       Date:  2021-03-12       Impact factor: 3.921

10.  Association of the Commitments and Responsibilities of the Caregiver Within the Family to the Disease Activity in Patients With Rheumatoid Arthritis: A Report From Turkey.

Authors:  Emel Sabaz Karakeci; Derya Çetintaş; Arzu Kaya
Journal:  Arch Rheumatol       Date:  2017-11-02       Impact factor: 1.472

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