Literature DB >> 22645226

"It's like we're grasping at anything": caregivers' education needs and preferred learning methods.

Beth Mastel-Smith1, Melinda Stanley-Hermanns.   

Abstract

In this qualitative descriptive study, we explored caregivers' educational needs and preferred methods of information delivery. Descriptions are based on five focus groups (N = 29) conducted with ethnically diverse, current and past family caregivers, including those who had previously attended a structured educational program. Themes arose from verbatim data transcriptions and coded themes. Four categories of educational needs were identified: (a) respite, (b) caregiving essentials, (c) self-care, and (d) the emotional aspects of caregiving. Advantages and disadvantages of learning methods are discussed, along with reasons for and outcomes of attending caregiver workshops. An informed caregiver model is proposed. Health care providers must assess educational needs and strive to provide appropriate information as dictated by the care recipient's condition and caregiver's expressed desires. Innovative methods of delivering information that are congruent with different caregiving circumstances and learning preferences must be developed and tested.

Mesh:

Year:  2012        PMID: 22645226     DOI: 10.1177/1049732312443739

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  8 in total

1.  Health literacy and medication administration performance by caregivers of adults with developmental disabilities.

Authors:  Steven R Erickson; Barbara LeRoy
Journal:  J Am Pharm Assoc (2003)       Date:  2015 Mar-Apr

2.  An emotional roller coaster - family members' experiences of being a caregiver throughout a cancer trajectory.

Authors:  Monica Solberg; Geir Vegard Berg; Hege Kristin Andreassen
Journal:  Int J Qual Stud Health Well-being       Date:  2022-12

3.  A qualitative study on perceptions of changes reported by caregivers of patients in vegetative state and minimally conscious state: the "time gap experience".

Authors:  Venusia Covelli; Milda Cerniauskaite; Matilde Leonardi; Davide Sattin; Alberto Raggi; Ambra Mara Giovannetti
Journal:  ScientificWorldJournal       Date:  2014-11-06

Review 4.  Exploring the evidence base for how people with dementia and their informal carers manage their medication in the community: a mixed studies review.

Authors:  Lydia Aston; Andrea Hilton; Tiago Moutela; Rachel Shaw; Ian Maidment
Journal:  BMC Geriatr       Date:  2017-10-18       Impact factor: 3.921

5.  Needs and preferences of informal caregivers regarding outpatient care for the elderly: a systematic literature review.

Authors:  M Plöthner; K Schmidt; L de Jong; J Zeidler; K Damm
Journal:  BMC Geriatr       Date:  2019-03-13       Impact factor: 3.921

6.  Effectiveness-implementation hybrid type 2 study evaluating an intervention to support 'information work' in dementia care: an implementation study protocol.

Authors:  Chiara De Poli; Jan R Oyebode; Christopher Binns; Richard Glover; Mara Airoldi
Journal:  BMJ Open       Date:  2020-12-08       Impact factor: 2.692

7.  The experiences of culturally and linguistically diverse family caregivers in utilising dementia services in Australia.

Authors:  Lily Dongxia Xiao; Anita De Bellis; Lesley Habel; Helena Kyriazopoulos
Journal:  BMC Health Serv Res       Date:  2013-10-22       Impact factor: 2.655

8.  Perceptions on technology for volunteer respite care for bedridden elders in Chile.

Authors:  Esmeralda Abarca; Solange Campos; Valeria Herskovic; Carolina Fuentes
Journal:  Int J Qual Stud Health Well-being       Date:  2018-12
  8 in total

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