Literature DB >> 24784235

Acceptance and valued living as critical appraisal and coping strengths for caregivers dealing with terminal illness and bereavement.

Esther L Davis1, Frank P Deane1, Geoffrey C B Lyons1.   

Abstract

OBJECTIVE: Informal caregivers of palliative care patients play an essential role in the coordination of care for patients during their final phases of life. However, undertaking a caregiving role can have enduring psychological consequences for caregivers and interfere with functioning. Studies have investigated a variety of factors associated with individual differences in caregiver psychosocial outcomes, but little is known about their relative impact, and there is a need for guiding models to support research in this area.
METHOD: A review of the literature was conducted on factors influencing the psychological distress and grief of caregivers. Drawing from acceptance and commitment therapy (ACT) and Stroebe and colleagues' integrative risk factor framework, we developed a process model to describe individual differences in caregiver psychological distress and grief.
RESULTS: The model presents caregiver psychological distress and grief as functions of death attitudes and communication about death and dying, mediated by acceptance and valued living from an ACT perspective. An outline of the empirical and theoretical underpinnings for each component in the model is provided. SIGNIFICANT OF
RESULTS: The presented model is an inherently strengths-based model that is concordant with acceptance- and values- (ACT) based interventions to facilitate coping in caregivers.

Entities:  

Keywords:  Theoretical model

Mesh:

Year:  2014        PMID: 24784235     DOI: 10.1017/S1478951514000431

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  6 in total

1.  Communication of emotion in home hospice cancer care: Implications for spouse caregiver depression into bereavement.

Authors:  Maija Reblin; Brian R W Baucom; Margaret F Clayton; Rebecca Utz; Michael Caserta; Dale Lund; Kathi Mooney; Lee Ellington
Journal:  Psychooncology       Date:  2019-04-05       Impact factor: 3.894

2.  Dehumanization and burden of care among caregivers of terminally ill patients.

Authors:  Ines Testoni; Giulia Sicari; Lucia Ronconi; Gianmarco Biancalani; Chiara Franco; Paolo Cottone; Robert Crupi
Journal:  Health Psychol Res       Date:  2021-10-07

3.  Psychological distress, health, and socio-economic factors in caregivers of terminally ill patients: a nationwide population-based cohort study.

Authors:  Mette Kjaergaard Nielsen; Mette Asbjoern Neergaard; Anders Bonde Jensen; Flemming Bro; Mai-Britt Guldin
Journal:  Support Care Cancer       Date:  2016-02-18       Impact factor: 3.603

4.  Impact of specialist home-based palliative care services in a tertiary oncology set up: a prospective non-randomized observational study.

Authors:  Sunil R Dhiliwal; Maryann Muckaden
Journal:  Indian J Palliat Care       Date:  2015 Jan-Apr

5.  A blended psychosocial support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: protocol of a randomized controlled trial.

Authors:  Jessica de Wit; Anita Beelen; Constance H C Drossaert; Ruud Kolijn; Leonard H van den Berg; Johanna M A Visser-Meily; Carin D Schröder
Journal:  BMC Psychol       Date:  2018-05-02

6.  Overcoming existential loneliness: a cross-cultural study.

Authors:  B P M Chung; J Olofsson; F K Y Wong; M Rämgård
Journal:  BMC Geriatr       Date:  2020-09-14       Impact factor: 3.921

  6 in total

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