Literature DB >> 24345081

Understanding social support burden among family caregivers.

Elaine Wittenberg-Lyles1, Karla Washington, George Demiris, Debra Parker Oliver, Sara Shaunfield.   

Abstract

Despite the abundance of research on social support, both as a variable in larger studies and as a central focus of examination, there is little consensus about the relationship between social support and health outcomes. Current social support measures typically account only for frequency and size of network, and a paucity of research exists that has explained social support burden, defined as the burden associated with accessing and receiving support from others. We analyzed audio-recorded discussions by hospice family caregivers about their caregiving problems and potential solutions to examine social relationships within networks and identify the processes that influence social support seeking and receiving. Using qualitative thematic analysis, we found that caregivers providing hospice care experience social support burden resulting from perceived relational barriers between friends and family, the inclination to remain in control, recognition of the loss of the patient as a source of social support and guidance in decision making, family dynamics, and decreased availability of emotional support. Social support researchers should consider how the quality of communication and relationships within social networks impacts the provision and subsequent outcomes of social support in varying contexts. Findings from this study suggest that hospice social support resources should be tailored to the caregiver's support needs and include assessment on the type of support to be offered.

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Year:  2013        PMID: 24345081      PMCID: PMC4029862          DOI: 10.1080/10410236.2013.815111

Source DB:  PubMed          Journal:  Health Commun        ISSN: 1041-0236


  23 in total

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  9 in total

1.  Exploring the Challenges that Family Caregivers Faced When Caring for Hospice Patients with Heart Failure.

Authors:  Nai-Ching Chi; George Demiris; Kenneth C Pike; Karla Washington; Debra Parker Oliver
Journal:  J Soc Work End Life Palliat Care       Date:  2018-06-01

2.  Support Network Factors Associated With Naming a Health Care Decision-Maker and Talking About Advance Care Planning Among People Living With HIV.

Authors:  Dulce M Cruz-Oliver; Tuo-Yen Tseng; Mary M Mitchell; Zachary Catanzarite; Chakra Budhathoki; Thomas J Smith; Cynda H Rushton; Amy R Knowlton
Journal:  J Pain Symptom Manage       Date:  2019-08-22       Impact factor: 3.612

3.  Factors influencing engagement in an online support group for family caregivers of individuals with advanced cancer.

Authors:  Karla T Washington; Debra Parker Oliver; Jacquelyn J Benson; Abigail J Rolbiecki; Lucas A Jorgensen; Dulce M Cruz-Oliver; George Demiris
Journal:  J Psychosoc Oncol       Date:  2019-11-06

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Authors:  Elaine Wittenberg-Lyles; Robin L Kruse; Debra Parker Oliver; George Demiris; Greg Petroski
Journal:  J Palliat Med       Date:  2013-12-18       Impact factor: 2.947

5.  The Social Convoy for Family Caregivers Over the Course of Hospice.

Authors:  David L Albright; Karla Washington; Debra Parker-Oliver; Alexandria Lewis; Robin L Kruse; George Demiris
Journal:  J Pain Symptom Manage       Date:  2015-11-03       Impact factor: 3.612

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Authors:  Maija Reblin; Gary Donaldson; Lee Ellington; Kathi Mooney; Michael Caserta; Dale Lund
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7.  Challenges and Strategies for Hospice Caregivers: A Qualitative Analysis.

Authors:  Debra Parker Oliver; George Demiris; Karla T Washington; Carlyn Clark; Deborah Thomas-Jones
Journal:  Gerontologist       Date:  2017-08-01

8.  Social support and subjective burden in caregivers of adults and older adults: A meta-analysis.

Authors:  Rafael Del-Pino-Casado; Antonio Frías-Osuna; Pedro A Palomino-Moral; María Ruzafa-Martínez; Antonio J Ramos-Morcillo
Journal:  PLoS One       Date:  2018-01-02       Impact factor: 3.240

9.  Development and feasibility of Inlife: A pilot study of an online social support intervention for informal caregivers of people with dementia.

Authors:  Alieske E H Dam; Martin P J van Boxtel; Nico Rozendaal; Frans R J Verhey; Marjolein E de Vugt
Journal:  PLoS One       Date:  2017-09-08       Impact factor: 3.240

  9 in total

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