Literature DB >> 3958409

Families of Alzheimer's victims. Family support to the caregivers.

J P Scott, K A Roberto, J T Hutton.   

Abstract

This study examined the instrumental and social-emotional support provided by families to the primary caregivers of Alzheimer's patients. It was anticipated that the more adequate the support provided by the family, the less sense of burden and the better the coping effectiveness of the caregiver. Ratings of instrumental assistance, social-emotional support, adequacy of support, and coping effectiveness were made by trained raters from transcribed interviews with 23 primary caregivers. Also, a second family member who was usually next closest of kin to the caregiver was interviewed in order to provide another perspective of the support the family provided. While the major caregiving tasks were performed by the primary caregiver, the types of assistance from family that seemed most appreciated were visits and having persons stay with the patient so that the caregiver could take a trip, rest, run errands, or get out of the house for social activities. The majority of caregivers felt a high degree of support from their families and reported low levels of emotional upset resulting from family support efforts. The most common family problems reported were lack of visits, disagreement over level of patient's mental and physical functioning, and disagreement over the type of care required. The data confirmed the hypothesis that family support was positively associated with the caregiver's coping effectiveness. In addition, caregivers who did not receive enough support were most burdened; however, the group receiving the greatest amount of support was the next most burdened, a finding which was unanticipated.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1986        PMID: 3958409     DOI: 10.1111/j.1532-5415.1986.tb04317.x

Source DB:  PubMed          Journal:  J Am Geriatr Soc        ISSN: 0002-8614            Impact factor:   5.562


  8 in total

Review 1.  Respite care for the chronically mentally ill: focus for the 1990s.

Authors:  D W Zirul; A A Lieberman; C A Rapp
Journal:  Community Ment Health J       Date:  1989

2.  Implications of caring for an aging parent.

Authors:  M J Yaffe
Journal:  CMAJ       Date:  1988-02-01       Impact factor: 8.262

3.  Caregiving networks-using a network approach to identify missed opportunities.

Authors:  Laura M Koehly; Sato Ashida; Ellen J Schafer; Amanda Ludden
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2014-09-14       Impact factor: 4.077

4.  Family, religion, and depressive symptoms in caregivers of disabled elderly.

Authors:  M V Zunzunegui; F Béland; A Llácer; I Keller
Journal:  J Epidemiol Community Health       Date:  1999-06       Impact factor: 3.710

5.  Audit of support given to lay carers of the demented elderly by a primary care team.

Authors:  I Philp; J Young
Journal:  J R Coll Gen Pract       Date:  1988-04

6.  Needs of caregivers of elderly attending day hospital.

Authors:  J Boxall; G McKercher
Journal:  Can Fam Physician       Date:  1990-01       Impact factor: 3.275

7.  Patterns of Caregiving Among Older Adults With and Without Dementia: A Latent Class Analysis.

Authors:  Talha Ali; Gail J McAvay; Joan K Monin; Thomas M Gill
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2022-05-20       Impact factor: 4.942

8.  Behavior disorders and subjective burden among caregivers of demented patients.

Authors:  Lucena Ferretti Ceres Eloah; Paulo Henrique Ferreira Bertolucci; Thaís Soares Cianciarullo Minett
Journal:  Dement Neuropsychol       Date:  2007 Apr-Jun
  8 in total

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