scholarly journals Family caregiver challenges in dementia care in Australia and China: a critical perspective

2014 ◽  
Vol 14 (1) ◽  
Author(s):  
Lily Dongxia Xiao ◽  
Jing Wang ◽  
Guo-Ping He ◽  
Anita De Bellis ◽  
Jenny Verbeeck ◽  
...  
2013 ◽  
Vol 70 (6) ◽  
pp. 1369-1380 ◽  
Author(s):  
Jing Wang ◽  
Lily Dongxia Xiao ◽  
Guo-Ping He ◽  
Anita De Bellis

2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 710-710
Author(s):  
Mary Wyman ◽  
Nickolas Lambrou ◽  
Debra Miller ◽  
Sunshine Wheelock ◽  
Florence Petri ◽  
...  

Abstract Prevalence of dementia among American Indian/Alaska Natives (AI/AN) is higher than in white populations, and AI/AN communities experience dementia care service gaps. This study explored perspectives within AI/AN communities regarding dementia, the family caregiver role, and home and community-based service use. Using tenets of Community-Based Participatory Research, qualitative interviews and a brief survey were conducted with 22 members of the Oneida Nation of Wisconsin (mean age 71 years, 73% female). Of the sample, 63.6% identified as a past or current family caregiver for a loved one with dementia. Awareness of services varied; 82% were aware of memory cafes, 75% knew of the caregiver support group, and 43% were familiar with dementia care specialist services. Thematic analysis revealed shared values of involving the family and community in dementia care, and offer guidance to support greater engagement in services. Implications for culturally-tailored service provision within AI/AN communities are discussed.


2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 941-941
Author(s):  
Emma Quach ◽  
Emily Franzosa ◽  
Rachael Scali ◽  
Lauren Moo ◽  
Christine Hartmann

Abstract Family caregiver support is a cornerstone of dementia care. Yet the transition to virtual care during COVID raised questions about the ability of dementia care teams to maintain caregiver support services. We surveyed Veterans Affairs clinicians about dementia caregiver support delivery following the COVID surge in the six New England states. 38 out of 68 (55%) clinicians from 6 states responded in June and July 2020. We found: 1) Clinicians continued providing the same types of support services for family caregivers before and after COVID, with over 50% of providers interacting with caregivers daily or multiple times per week. The most prevalent services were caregiver needs assessments, information and referrals, and assistance with accessing services. Two-thirds reported continuing to offer caregiver skills training and counseling, including peer support groups. 2) Caregiver support modality changed, most frequently through the combined use of phone and video, followed by only phone, and rarely, by only video. 3) Providers indicated that phone, more than video, increased to replace in-person interactions, because of multiple factors: caregivers (who continued to call for support on an as-needed basis but declined video encounters), providers (who began to provide group support via phone), and service factors (ad hoc versus scheduled encounters). Results suggest clinicians continued providing caregiver support despite suspension of in-person interactions, but future research is needed to assess the impacts of caregiver support delivery mostly by phone and factors underlying the limited use of video in delivering caregiver support.


Pflege ◽  
2005 ◽  
Vol 18 (01) ◽  
pp. 0067-0067
Author(s):  
Christina Anthea

Sign in / Sign up

Export Citation Format

Share Document