Literature DB >> 23335153

Reducing the psychological distress of family caregivers of home-based palliative care patients: short-term effects from a randomised controlled trial.

Peter Hudson1, Tom Trauer, Brian Kelly, Moira O'Connor, Kristina Thomas, Michael Summers, Rachel Zordan, Vicki White.   

Abstract

BACKGROUND: Palliative care is expected to incorporate comprehensive support for family caregivers given that many caregivers suffer psychological morbidity. However, systematically implemented evidence-based psychological support initiatives are lacking. AIM: The objective of this study was to prepare caregivers for the role of supporting a patient with advanced cancer receiving home-based palliative care by offering a one-to-one psycho-educational intervention. We hypothesised that primary family caregivers who participated in the intervention would report decreased psychological distress (primary outcome), fewer unmet needs and increased levels of perceived preparedness, competence and positive emotions.
METHODS: A three-arm randomised controlled trial was conducted comparing two versions of the intervention (one face-to-face visit versus two visits) plus standard care to a control group (standard care) across four sites in Australia.
RESULTS: A total of 298 participants were recruited; 148 were in the Control condition, 57 in Intervention 1 (one visit) and 93 in Intervention 2 (two visits). Relative to participants in the control group; the psychological well-being of participants in the intervention condition was improved by a small amount but non-significantly. No significant reduction in unmet needs or improvements in positive aspects of caregiving amongst the intervention group were identified. However, the intervention demonstrated significant improvements in participants' levels of preparedness and competence for Intervention 2. CONCLUSION/IMPLICATIONS: This research adds to accumulating body of evidence demonstrating that relatively short psycho-educational interventions can enable family caregivers to feel more prepared and competent in the role of supporting a dying relative. Further investigation is required to determine the longer term outcomes of such interventions.
Copyright © 2013 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2013        PMID: 23335153     DOI: 10.1002/pon.3242

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  25 in total

1.  Interventions to help support caregivers of people with a brain or spinal cord tumour.

Authors:  Florien W Boele; Alasdair G Rooney; Helen Bulbeck; Paula Sherwood
Journal:  Cochrane Database Syst Rev       Date:  2019-07-02

2.  Improving information to caregivers of cancer patients: the Herlev Hospital Empowerment of Relatives through More and Earlier information Supply (HERMES) randomized controlled trial.

Authors:  Line Lund; Lone Ross; Morten Aagaard Petersen; Lisa Sengelov; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2019-06-08       Impact factor: 3.603

3.  Informal caregiver quality of life in a palliative oncology population.

Authors:  Adele Duimering; Jill Turner; Karen Chu; Fleur Huang; Diane Severin; Sunita Ghosh; Don Yee; Ericka Wiebe; Nawaid Usmani; Zsolt Gabos; Samir Patel; Brita Danielson; John Amanie; Wilson Roa; Alysa Fairchild
Journal:  Support Care Cancer       Date:  2019-07-10       Impact factor: 3.603

4.  Specialized home palliative care for adults and children: differences and similarities.

Authors:  Gesa Groh; Berend Feddersen; Monika Führer; Gian Domenico Borasio
Journal:  J Palliat Med       Date:  2014-06-13       Impact factor: 2.947

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Journal:  Epidemiol Rev       Date:  2017-01-01       Impact factor: 6.222

Review 6.  [Cancer and family: tasks and stress of relatives].

Authors:  V Popek; K Hönig
Journal:  Nervenarzt       Date:  2015-03       Impact factor: 1.214

7.  Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care.

Authors:  Heide Götze; Elmar Brähler; Lutz Gansera; Nina Polze; Norbert Köhler
Journal:  Support Care Cancer       Date:  2014-05-09       Impact factor: 3.603

8.  Predicting distress among people who care for patients living longer with high-grade malignant glioma.

Authors:  B Russell; A Collins; A Dowling; M Dally; M Gold; M Murphy; J Burchell; J Philip
Journal:  Support Care Cancer       Date:  2015-04-25       Impact factor: 3.603

9.  Effectiveness of an interdisciplinary palliative care intervention for family caregivers in lung cancer.

Authors:  Virginia Sun; Marcia Grant; Marianna Koczywas; Bonnie Freeman; Finly Zachariah; Rebecca Fujinami; Catherine Del Ferraro; Gwen Uman; Betty Ferrell
Journal:  Cancer       Date:  2015-07-06       Impact factor: 6.860

10.  A systematic review of interventions for family caregivers who care for patients with advanced cancer at home.

Authors:  Soojung Ahn; Rafael D Romo; Cathy L Campbell
Journal:  Patient Educ Couns       Date:  2020-03-12
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