573 related articles for article (PubMed ID: 27662829)
1. In the Information Age, do dementia caregivers get the information they need? Semi-structured interviews to determine informal caregivers' education needs, barriers, and preferences.
Peterson K; Hahn H; Lee AJ; Madison CA; Atri A
BMC Geriatr; 2016 Sep; 16(1):164. PubMed ID: 27662829
[TBL] [Abstract][Full Text] [Related]
2. Rural and remote dementia care challenges and needs: perspectives of formal and informal care providers residing in Saskatchewan, Canada.
Dal Bello-Haas VP; Cammer A; Morgan D; Stewart N; Kosteniuk J
Rural Remote Health; 2014; 14(3):2747. PubMed ID: 25081857
[TBL] [Abstract][Full Text] [Related]
3. Family Caregiver Needs and Preferences for Virtual Training to Manage Behavioral and Psychological Symptoms of Dementia: Interview Study.
Ramirez M; Duran MC; Pabiniak CJ; Hansen KE; Kelley A; Ralston JD; McCurry SM; Teri L; Penfold RB
JMIR Aging; 2021 Feb; 4(1):e24965. PubMed ID: 33565984
[TBL] [Abstract][Full Text] [Related]
4. Understanding Internet Use Among Dementia Caregivers: Results of Secondary Data Analysis Using the US Caregiver Survey Data.
Kim H
Interact J Med Res; 2015 Feb; 4(1):e1. PubMed ID: 25707033
[TBL] [Abstract][Full Text] [Related]
5. Effectiveness of interventions that assist caregivers to support people with dementia living in the community: a systematic review.
Parker D; Mills S; Abbey J
Int J Evid Based Healthc; 2008 Jun; 6(2):137-72. PubMed ID: 21631819
[TBL] [Abstract][Full Text] [Related]
6. Family caregivers' support needs after brain injury: a synthesis of perspectives from caregivers, programs, and researchers.
Gan C; Gargaro J; Brandys C; Gerber G; Boschen K
NeuroRehabilitation; 2010; 27(1):5-18. PubMed ID: 20634597
[TBL] [Abstract][Full Text] [Related]
7. "I just don't focus on my needs." The unmet health needs of partner and offspring caregivers of people with dementia: A qualitative study.
Tatangelo G; McCabe M; Macleod A; You E
Int J Nurs Stud; 2018 Jan; 77():8-14. PubMed ID: 28982034
[TBL] [Abstract][Full Text] [Related]
8. Features of primary care practice influence emergency care-seeking behaviors by caregivers of persons with dementia: A multiple-perspective qualitative study.
Beck AP; Jacobsohn GC; Hollander M; Gilmore-Bykovskyi A; Werner N; Shah MN
Dementia (London); 2021 Feb; 20(2):613-632. PubMed ID: 32050779
[TBL] [Abstract][Full Text] [Related]
9. Accessing community dementia care services in Ireland: Emotional barriers for caregivers.
Ryan L
Health Soc Care Community; 2021 Nov; 29(6):1980-1989. PubMed ID: 33682982
[TBL] [Abstract][Full Text] [Related]
10. Unmet needs of caregivers of individuals referred to a dementia care program.
Jennings LA; Reuben DB; Evertson LC; Serrano KS; Ercoli L; Grill J; Chodosh J; Tan Z; Wenger NS
J Am Geriatr Soc; 2015 Feb; 63(2):282-9. PubMed ID: 25688604
[TBL] [Abstract][Full Text] [Related]
11. Getting what they need when they need it. Identifying barriers to information needs of family caregivers to manage dementia-related behavioral symptoms.
Werner NE; Stanislawski B; Marx KA; Watkins DC; Kobayashi M; Kales H; Gitlin LN
Appl Clin Inform; 2017 Feb; 8(1):191-205. PubMed ID: 28224163
[TBL] [Abstract][Full Text] [Related]
12. Knowledge exchange throughout the dementia care journey by Canadian rural community-based health care practitioners, persons with dementia, and their care partners: an interpretive descriptive study.
Forbes DA; Finkelstein S; Blake CM; Gibson M; Morgan DG; Markle-Reid M; Culum I; Thiessen E
Rural Remote Health; 2012 Oct; 12(4):2201. PubMed ID: 23176308
[TBL] [Abstract][Full Text] [Related]
13. Health information management practices in informal caregiving: An artifacts analysis and implications for IT design.
Holden RJ; Karanam YLP; Cavalcanti LH; Parmar T; Kodthala P; Fowler NR; Bateman DR
Int J Med Inform; 2018 Dec; 120():31-41. PubMed ID: 30409344
[TBL] [Abstract][Full Text] [Related]
14. Hearing Their Voice: A Systematic Review of Dementia Family Caregivers' Needs.
McCabe M; You E; Tatangelo G
Gerontologist; 2016 Oct; 56(5):e70-88. PubMed ID: 27102056
[TBL] [Abstract][Full Text] [Related]
15. A process-based approach to exploring the information behavior of informal caregivers of people living with dementia.
Rutkowski RA; Ponnala S; Younan L; Weiler DT; Bykovskyi AG; Werner NE
Int J Med Inform; 2021 Jan; 145():104341. PubMed ID: 33242761
[TBL] [Abstract][Full Text] [Related]
16. Health-Related Internet Use by Informal Caregivers of Children and Adolescents: An Integrative Literature Review.
Park E; Kim H; Steinhoff A
J Med Internet Res; 2016 Mar; 18(3):e57. PubMed ID: 26940750
[TBL] [Abstract][Full Text] [Related]
17. "There isn't an easy way of finding the help that's available." Barriers and facilitators of service use among dementia family caregivers: a qualitative study.
Macleod A; Tatangelo G; McCabe M; You E
Int Psychogeriatr; 2017 May; 29(5):765-776. PubMed ID: 28351450
[TBL] [Abstract][Full Text] [Related]
18. Family caregiver challenges in dementia care in a country with undeveloped dementia services.
Wang J; Xiao LD; He GP; De Bellis A
J Adv Nurs; 2014 Jun; 70(6):1369-80. PubMed ID: 24192338
[TBL] [Abstract][Full Text] [Related]
19. Capturing the perspectives of African American informal dementia caregivers: a phenomenological study.
Assfaw AD; Reinschmidt KM; Teasdale TA; Stephens L; Kleszynski KL; Dwyer K
Ethn Health; 2024 Jun; ():1-18. PubMed ID: 38937933
[TBL] [Abstract][Full Text] [Related]
20. Intersection of multiple factors shape Korean American caregiver experience in dementia caregiving.
Joo J; Choi S; Gallo JJ; Han H; Kim S; Xu J; Yeom S
Aging Ment Health; 2023; 27(10):1975-1982. PubMed ID: 37278694
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
