Literature DB >> 29564712

A systematic review of Indigenous caregiver functioning and interventions.

Lesli Hokanson1, Michael Gerhardt Quinn1, Natalie Schüz1,2, Kristy de Salas1, Jenn Scott3.   

Abstract

PURPOSE: There is a global increase in chronic, degenerative illnesses that require long-term intervention and support as a result of the aging population. The majority of support needs are met by informal family caregivers. While there have been three decades of research focusing on caregivers in general, the extent to which research has focused on Indigenous caregivers is unclear. Worldwide, Indigenous peoples face severe economic and health disadvantages that may make them even more vulnerable to the negative aspects of informal caregiving. The current systematic review aimed to synthesize the extant literature on Indigenous caregiver functioning and the interventions that are efficacious in alleviating Indigenous caregiver distress.
METHODS: Systematic review Inclusion criteria were peer-reviewed quantitative studies examining Indigenous caregiver functioning or evaluating Indigenous caregiver interventions.
RESULTS: 1172 unique records were located in the final search undertaken; only 7 articles, representing 6 unique studies, met the full inclusion criteria. Most studies contained numerous methodological weaknesses that compromised the reliability and validity of findings. Available studies suggest poor health and high burden among Indigenous relative to non-Indigenous caregivers. However, high levels of positive aspects of caregiving were reported in one study. A single intervention study suggests that poor health outcomes among Indigenous caregivers can be alleviated, though the quality and focus of this study was sub-optimal.
CONCLUSIONS: Overall, there is very little quality evidence around Indigenous caregiver functioning. Future research in this area would benefit from greater adherence to the standards of research that contribute to a strong and reliable evidence base.

Entities:  

Keywords:  Caregiving; Coping; Family caregivers; Indigenous; Psychological functioning; Systematic review

Mesh:

Year:  2018        PMID: 29564712     DOI: 10.1007/s11136-018-1836-1

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  31 in total

1.  Toward the conceptualization and measurement of caregiver burden among Pueblo Indian family caregivers.

Authors:  R John; C H Hennessy; T B Dyeson; M D Garrett
Journal:  Gerontologist       Date:  2001-04

Review 2.  Differences between caregivers and noncaregivers in psychological health and physical health: a meta-analysis.

Authors:  Martin Pinquart; Silvia Sörensen
Journal:  Psychol Aging       Date:  2003-06

3.  Improving the reporting quality of nonrandomized evaluations of behavioral and public health interventions: the TREND statement.

Authors:  Don C Des Jarlais; Cynthia Lyles; Nicole Crepaz
Journal:  Am J Public Health       Date:  2004-03       Impact factor: 9.308

4.  Racial inequality in active life among adult Americans.

Authors:  M D Hayward; M Heron
Journal:  Demography       Date:  1999-02

5.  The experience of whanau caring for members disabled from the effects of a cerebro-vascular accident.

Authors:  Andrea Corbett; Karen Francis; Ysanne Chapman
Journal:  Contemp Nurse       Date:  2006-09       Impact factor: 1.787

6.  The role of attitudes and culture in family caregiving for older adults.

Authors:  Linda Anngela-Cole; Jeanne M Hilton
Journal:  Home Health Care Serv Q       Date:  2009

7.  Influence of caregiving on health-related quality of life among American Indians.

Authors:  S Melinda Spencer; R Turner Goins; Jeffrey A Henderson; Yang Wen; Jack Goldberg
Journal:  J Am Geriatr Soc       Date:  2013-09-03       Impact factor: 5.562

8.  A randomized trial of a CAM therapy for stress reduction in American Indian and Alaskan Native family caregivers.

Authors:  Leslie Korn; Rebecca G Logsdon; Nayak L Polissar; Alfredo Gomez-Beloz; Tiffany Waters; Rudolph Rÿser
Journal:  Gerontologist       Date:  2009-04-18

9.  [Burden of care in Aymara caregivers of patients with schizophrenia].

Authors:  Alejandra Caqueo-Urízar; José Gutiérrez-Maldonado; Marta Ferrer-García; Paulina Darrigrande-Molina
Journal:  Rev Psiquiatr Salud Ment       Date:  2011-09-19       Impact factor: 3.318

10.  Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation.

Authors:  Larissa Shamseer; David Moher; Mike Clarke; Davina Ghersi; Alessandro Liberati; Mark Petticrew; Paul Shekelle; Lesley A Stewart
Journal:  BMJ       Date:  2015-01-02
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  3 in total

1.  A comparison of psychometric properties of two common measures of caregiving burden: the family burden interview schedule (FBIS-24) and the Zarit caregiver burden interview (ZBI-22).

Authors:  Yu Yu; Zi-Wei Liu; Tong-Xin Li; Wei Zhou; Shi-Jun Xi; Shui-Yuan Xiao; Jacob Kraemer Tebes
Journal:  Health Qual Life Outcomes       Date:  2020-04-06       Impact factor: 3.186

2.  Understanding Aboriginal Peoples' Cultural and Family Connections Can Help Inform the Development of Culturally Appropriate Cancer Survivorship Models of Care.

Authors:  Eli Ristevski; Sharyn Thompson; Sharon Kingaby; Claire Nightingale; Mahesh Iddawela
Journal:  JCO Glob Oncol       Date:  2020-02

3.  Māori elders' perspectives of end-of-life family care: whānau carers as knowledge holders, weavers, and navigators.

Authors:  Mary Louisa Simpson; Kirstie McAllum; John Oetzel; Kay Berryman; Rangimahora Reddy
Journal:  Palliat Care Soc Pract       Date:  2022-09-08
  3 in total

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