Literature DB >> 16410438

The meaning of family caregiving in Japan and the United States: a qualitative comparative study.

Margaret I Wallhagen1, Noriko Yamamoto-Mitani.   

Abstract

This study explores how cultural values affect the meaning and experiences of daughter (or daughter-in-law) caregivers of elderly persons with dementia by comparing caregivers in the United States and Japan. Nine American and seven Japanese caregivers were interviewed twice at 6-month intervals. Interviews were audiotaped and analyzed using constant-comparative techniques. Data suggest that moral obligation to care and intense loss are two universal themes of caregiving. However the experiences and perceptions of the role of caregivers from these two cultures differed in select ways that were captured within three categories: reasons for caregiving, caregiving as a career, and caregiving as a life phase or detour. Findings suggest that American caregivers may need greater anticipatory socialization regarding the caregiving role, whereas Japanese caregivers may benefit from assistance in accepting needed services.

Entities:  

Mesh:

Year:  2006        PMID: 16410438     DOI: 10.1177/1043659605281979

Source DB:  PubMed          Journal:  J Transcult Nurs        ISSN: 1043-6596            Impact factor:   1.959


  9 in total

1.  Evaluative and Experienced Well-being of Caregivers of Parents and Caregivers of Children.

Authors:  Anna M Hammersmith; I-Fen Lin
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2019-01-10       Impact factor: 4.077

2.  Guardians of health: the dimensions of elder caregiving among women in a Mexico City neighborhood.

Authors:  Carolyn A Mendez-Luck; David P Kennedy; Steven P Wallace
Journal:  Soc Sci Med       Date:  2008-11-24       Impact factor: 4.634

3.  Caregiving experiences of family members of persons with dementia in south India.

Authors:  Suzanne M Narayan; Mathew Varghese; Kenneth Hepburn; Marsha Lewis; Isabel Paul; Rozina Bhimani
Journal:  Am J Alzheimers Dis Other Demen       Date:  2015-03-03       Impact factor: 2.632

4.  Sharing in the life of the person with disability: A Ghanaian perspective.

Authors:  Frances E Owusu-Ansah
Journal:  Afr J Disabil       Date:  2015-09-29

5.  Experiences of end of life amongst family carers of people with advanced dementia: longitudinal cohort study with mixed methods.

Authors:  Kirsten J Moore; Sarah Davis; Anna Gola; Jane Harrington; Nuriye Kupeli; Victoria Vickerstaff; Michael King; Gerard Leavey; Irwin Nazareth; Louise Jones; Elizabeth L Sampson
Journal:  BMC Geriatr       Date:  2017-07-03       Impact factor: 3.921

6.  Motivations for being informal carers of people living with dementia: a systematic review of qualitative literature.

Authors:  Nan Greenwood; Raymond Smith
Journal:  BMC Geriatr       Date:  2019-06-17       Impact factor: 3.921

7.  What We Talk about When We Talk about Caregiving: The Distribution of Roles in Cancer Patient Caregiving in a Family-Oriented Culture.

Authors:  Ansuk Jeong; Dongwook Shin; Jong Hyock Park; Keeho Park
Journal:  Cancer Res Treat       Date:  2018-03-21       Impact factor: 4.679

Review 8.  How Culture Shapes Informal Caregiver Motivations: A Meta-Ethnographic Review.

Authors:  Mikołaj Zarzycki; Diane Seddon; Eva Bei; Rachel Dekel; Val Morrison
Journal:  Qual Health Res       Date:  2022-06-23

9.  Pre-decision regret before transition of dependents with severe dementia to long-term care.

Authors:  Ingrid Hanssen; Flora M Mkhonto; Hilde Øieren; Malmsey Lm Sengane; Anne Lene Sørensen; Phuong Thai Minh Tran
Journal:  Nurs Ethics       Date:  2021-09-28       Impact factor: 2.874

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.