Journal articles on the topic 'Informal Care'

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1

Penrod, Joan D., Katherine M. Harris, and Robert L. Kane. "Informal Care Substitution:." Journal of Aging & Social Policy 6, no. 4 (June 2, 1995): 21–31. http://dx.doi.org/10.1300/j031v06n04_03.

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2

Saunders, Hilary, and Julie Selwyn. "Supporting Informal Kinship Care." Adoption & Fostering 32, no. 2 (July 2008): 31–42. http://dx.doi.org/10.1177/030857590803200205.

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3

Evers, Adalbert, and Kai Leichsenring. "Paying for informal care." Ageing International 21, no. 1 (March 1994): 29–40. http://dx.doi.org/10.1007/bf02681177.

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4

Kwak, Minyoung, BoRin Kim, Hyunjoo Lee, and Jiaan Zhang. "Gender Matters in the Receipt of Informal Care in Later Life: A Cross-National Comparison Across the USA, Korea, and China." Innovation in Aging 4, Supplement_1 (December 1, 2020): 560. http://dx.doi.org/10.1093/geroni/igaa057.1845.

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Abstract This study compares patterns of gender difference in the receipt of informal care among community-dwelling older adults across the United States, Korea, and China. Data came from the 2014 HRS, the 2014 KLoSA, and the 2015 CHARLS. Logistic regression models were used to predict the receipt of informal care by gender. We also examined how the effects of health and living arrangement on the receipt of informal care differ depending on gender. In the United States and China, older women were more likely to receive informal care than men. However, older Korean women were less likely to receive informal care than men. The effects of health and living arrangement on the use of informal care were moderated by gender in different ways across countries. Discussions include implications for practice and policy to reduce the gender gap in the receipt of informal care.
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5

Nelson, Hilde Lindemann, and Carol Levine. "The Cost of "Informal" Care." Hastings Center Report 31, no. 4 (July 2001): 47. http://dx.doi.org/10.2307/3527956.

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6

del Río-Lozano, María, María del Mar García-Calvente, Jorge Marcos-Marcos, Francisco Entrena-Durán, and Gracia Maroto-Navarro. "Gender Identity in Informal Care." Qualitative Health Research 23, no. 11 (October 4, 2013): 1506–20. http://dx.doi.org/10.1177/1049732313507144.

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7

Dewey, H. M., A. G. Thrift, C. Mihalopoulos, R. Carter, R. A. L. Macdonell, J. J. McNeil, and G. A. Donnan. "Informal Care for Stroke Survivors." Stroke 33, no. 4 (April 2002): 1028–33. http://dx.doi.org/10.1161/01.str.0000013067.24300.b0.

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8

Al-Janabi, Hareth, Fiona Carmichael, and Jan Oyebode. "Informal care: choice or constraint?" Scandinavian Journal of Caring Sciences 32, no. 1 (April 12, 2017): 157–67. http://dx.doi.org/10.1111/scs.12441.

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9

Lawson, Douglas, and James W. Fleshman. "Informal Leadership in Health Care." Clinics in Colon and Rectal Surgery 33, no. 04 (June 3, 2020): 225–27. http://dx.doi.org/10.1055/s-0040-1709439.

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AbstractInformal leaders in nursing, medical specialties, and administration positively impact the success of an institution. Developing all members of the team as leader then becomes important, especially in the area of nursing. The result is less need for management and control and more individual self-motivated participation in quality improvement.
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10

Muurinen, Janna-Marja. "The Economics of Informal Care." Medical Care 24, no. 11 (November 1986): 1007–17. http://dx.doi.org/10.1097/00005650-198611000-00005.

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11

Da Roit, Barbara, Marcel Hoogenboom, and Bernhard Weicht. "The Gender Informal Care Gap." European Societies 17, no. 2 (February 23, 2015): 199–218. http://dx.doi.org/10.1080/14616696.2015.1007153.

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12

Vlachantoni, A., M. Evandrou, J. Falkingham, and J. Robards. "Informal care, health and mortality." Maturitas 74, no. 2 (February 2013): 114–18. http://dx.doi.org/10.1016/j.maturitas.2012.10.013.

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13

Rhodes, Penny, and Sandra Shaw. "Informal care and terminal illness." Health & Social Care in the Community 7, no. 1 (January 1999): 39–50. http://dx.doi.org/10.1046/j.1365-2524.1999.00147.x.

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14

Bond, John. "Informal Care and Social Support." Ageing and Society 10, no. 4 (December 1990): 469–75. http://dx.doi.org/10.1017/s0144686x00007431.

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15

van den Berg, B. "PMI16: VALUATION OF INFORMAL CARE." Value in Health 4, no. 6 (September 2001): 426–27. http://dx.doi.org/10.1016/s1098-3015(11)71550-9.

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16

Bayen, E., C. Papeix, P. Pradat-Diehl, C. Lubetzki, and M. E. Joël. "Informal care in multiple sclerosis." Annals of Physical and Rehabilitation Medicine 58 (September 2015): e105. http://dx.doi.org/10.1016/j.rehab.2015.07.255.

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17

Horsley, S., S. Barrow, N. Gent, and J. Astbury. "Informal care and psychiatric morbidity." Journal of Public Health 20, no. 2 (June 1, 1998): 180–85. http://dx.doi.org/10.1093/oxfordjournals.pubmed.a024740.

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18

Caro, Francis G., and Amy Leventhal Stern. "Balancing Formal and Informal Care." Home Health Care Services Quarterly 15, no. 4 (June 27, 1996): 67–81. http://dx.doi.org/10.1300/j027v15n04_05.

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19

Tennstedt, Sharon L., Brooke Harrow, and Sybil Crawford. "Informal Care vs. Formal Services." Journal of Aging & Social Policy 7, no. 3-4 (June 26, 1996): 71–92. http://dx.doi.org/10.1300/j031v07n03_05.

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20

Sherwood, Sylvia, and Ellen Bernstein. "Informal Care for Vulnerable Elderly:." Journal of Religion & Aging 2, no. 1-2 (February 18, 1986): 55–67. http://dx.doi.org/10.1300/j491v02n01_05.

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21

Holmes, Ann M., and Partha Deb. "Factors influencing informal care-giving." Journal of Mental Health Policy and Economics 1, no. 2 (July 1998): 77–87. http://dx.doi.org/10.1002/(sici)1099-176x(199807)1:2<77::aid-mhp10>3.0.co;2-5.

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22

Mommaerts, Corina, and Yulya Truskinovsky. "The cyclicality of informal care." Journal of Health Economics 71 (May 2020): 102306. http://dx.doi.org/10.1016/j.jhealeco.2020.102306.

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23

van den Berg, Bernard, Werner B. F. Brouwer, and Marc A. Koopmanschap. "Economic valuation of informal care." European Journal of Health Economics 5, no. 1 (February 1, 2004): 36–45. http://dx.doi.org/10.1007/s10198-003-0189-y.

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24

Do, Young Kyung, Edward C. Norton, Sally C. Stearns, and Courtney Harold Van Houtven. "Informal Care and Caregiver's Health." Health Economics 24, no. 2 (April 17, 2014): 224–37. http://dx.doi.org/10.1002/hec.3012.

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25

Singh, Prabhjot, Rafat Hussain, Adeel Khan, Lyn Irwin, and Roslyn Foskey. "Dementia Care: Intersecting Informal Family Care and Formal Care Systems." Journal of Aging Research 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/486521.

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Dementia is one of the major causes of disability and dependence amongst older people and previous research has highlighted how the well-being of people with dementia is inherently connected to the quality of their relationships with their informal carers. In turn, these carers can experience significant levels of emotional stress and physical burden from the demands of caring for a family member with dementia, yet their uptake of formal services tends to be lower than in other conditions related to ageing. This paper is based on a qualitative study undertaken in the Australian state of Queensland and explores issues of access to and use of formal services in dementia care from the perspective of the informal family carers. It identifies three critical points at which changes in policy and practice in the formal care system could improve the capability of informal carers to continue to care for their family member with dementia: when symptoms first become apparent and a diagnosis is sought; when the condition of the person with dementia changes resulting in a change to their support needs; and when the burden of informal care being experienced by the carer is so great that some form of transition appears to be immanent in the care arrangement.
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26

McPherson, Lorraine, Stuart Milligan, and Elaine Stevens. "Participating in the personal care of a person living with a life-limiting illness in a hospice inpatient setting: the informal caregiver's perspective." International Journal of Palliative Nursing 26, no. 5 (June 2, 2020): 246–57. http://dx.doi.org/10.12968/ijpn.2020.26.5.246.

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Methods: Using semi-structured interviews, this descriptive qualitative research study examined informal caregivers' perspectives of participating in the personal care of a person living with a life-limiting illness within one hospice inpatient setting. Some 10 principal, informal caregivers of hospice inpatients were recruited by means of purposive sampling, using posters displayed in the hospice inpatient unit. Thus, participation was entirely ‘opt-in’. A flash card was displayed at the beginning of each interview to determine a definition of personal care. Field notes and digital audio recording were used to capture data collected. Results: Data were thematically analysed and demonstrated that informal caregivers' perceptions of personal care included everything that allowed the patient to remain the person they were. Informal caregivers reported an acceptable balance between being able to carry out personal care and hospice nursing staff involvement, despite no discussions being carried out to establish their wishes. Prior experiences of informal caregiving, and individual caregiver preparedness, contributed to negative and positive feelings about participating in personal care. Informal caregivers reported additional support and education needs associated with being able to participate in the personal care of patients on discharge and in the future. Conclusions: The emergent themes provide palliative care practitioners with direction for professional practice and research around supporting informal caregivers participating in personal care. Healthcare professionals need to clarify terminology of personal care by having dialogues with informal caregivers and acting on these accordingly. However, not all informal caregivers want such conversations. Consequently, healthcare professionals should approach this topic sensitively. Healthcare professionals ought to be asking informal caregivers if they wish to participate in personal care. Hospice nurses need to engage, support and educate informal caregivers about personal care. Furthermore, they should help to maintain and develop the skills of those informal caregivers who want to continue to play this role and not allow them to become deskilled.
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27

Wang, Yixiao. "Impact of Informal Care on Health Care Utilization Among Older People in China." Innovation in Aging 5, Supplement_1 (December 1, 2021): 332. http://dx.doi.org/10.1093/geroni/igab046.1289.

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Abstract Population aging has become a challenge to long-term care and health care for the society. Using China as a case study, this paper assesses allocative efficiency of resources in informal care and health care, to explore the effectiveness of the policy, i.e., encouraging informal care as a more cost-effective way to reduce public health care spending. Drawing data from the 2011, 2014, and 2018 waves of the Chinese Longitudinal Healthy Longevity Survey, this study examines the impact of informal care on utilization of health care as well as amount of health care expenditures among older people with functional limitations in China. Using random effects model with instrumental variable approach, our findings suggest that informal care significantly reduces the utilization of health care, primarily by reducing the utilization of outpatient care. However, informal care significantly increases the amount of inpatient care expenditures for inpatient care users. We do not observe significant association between informal care and amount of outpatient care expenditures for outpatient care users. This study highlights a pressing need for the Chinese government to support informal caregivers by taking economic values of informal caregiving into consideration, and to improve efficiency in inpatient care by a more integrated resource allocation mechanism
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28

McCann, S., and D. S. Evans. "Informal care: the views of people receiving care." Health and Social Care in the Community 10, no. 4 (July 2002): 221–28. http://dx.doi.org/10.1046/j.1365-2524.2002.00367.x.

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29

Zhang, Huimin, Xiaoyi Zhang, Youhua Zhao, Jianfeng Huang, and Wenwei Liu. "Impact of Formal Care Use on Informal Care from Children after the Launch of Long-Term Care Insurance in Shanghai, China." International Journal of Environmental Research and Public Health 17, no. 8 (April 24, 2020): 2938. http://dx.doi.org/10.3390/ijerph17082938.

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The impact of formal care (co-paid by long term care (LTC) insurance) on informal care is critical to the improvement and promotion of public policy. We conducted an interview-based survey to examine how the use of formal care impacts the use of informal care in Shanghai, which was one of China’s first long-term insurance pilots in 2016. In addition to total informal care time, the following four types of informal care were considered: (1) household activities of daily living (HDL) tasks, (2) activities of daily living (ADL) tasks, (3) instrumental activities of daily living (IADL) tasks, and (4) supervision tasks. Of the 407 families, an average of 12.36 h (SD = 6.70) of informal care was crowded out each week. Among them, ADL tasks, HDL tasks, and supervision tasks were reduced an average of 4.60 (SD = 3.59), 5.50 (SD = 3.38), and 2.10 h (SD = 3.06) per week, respectively. Each additional hour of formal care reduced 0.473 h of informal care. Care recipients’ gender and health status were also determined to be associated with crowding out hours of informal care. These findings can be utilized as empirical evidence for decision-makers to consider the scope of funding for formal care, and this study provides comparable results to developing countries and regions.
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30

TOLKACHEVA, NATALIA, MARJOLEIN BROESE VAN GROENOU, ALICE DE BOER, and THEO VAN TILBURG. "The impact of informal care-giving networks on adult children's care-giver burden." Ageing and Society 31, no. 1 (September 17, 2010): 34–51. http://dx.doi.org/10.1017/s0144686x10000711.

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ABSTRACTPrevious research on the care-giver burden experienced by adult children has typically focused on the adult child and parent dyad. This study uses information on multiple informal care-givers and examines how characteristics of the informal care-giving network affect the adult child's care-giver burden. In 2007, 602 Dutch care-givers who were assisting their older parents reported on parental and personal characteristics, care activities, experienced burden and characteristics of other informal care-givers. A path model was applied to assess the relative impact of the informal care-giving network characteristics on the care-giver burden. An adult child experienced lower care-giver burden when the informal care-giving network size was larger, when more types of tasks were shared across the network, when care was shared for a longer period, and when the adult child had no disagreements with the other members of the network. Considering that the need for care of older parents is growing, being in an informal care-giving network will be of increasing benefit for adult children involved in long-term care. More care-givers will turn into managers of care, as they increasingly have to organise the sharing of care among informal helpers and cope with disagreements among the members of the network.
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31

Andersson, Agneta, John Carstensen, Lars-Åke Levin, and Bengt Göran Emtinger. "COSTS OF INFORMAL CARE FOR PATIENTS IN ADVANCED HOME CARE: A POPULATION-BASED STUDY." International Journal of Technology Assessment in Health Care 19, no. 4 (December 2003): 656–63. http://dx.doi.org/10.1017/s0266462303000618.

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Objectives: Several studies have sought to analyze the cost-effectiveness of advanced home care and home rehabilitation. However, the costs of informal care are rarely included in economic appraisals of home care. This study estimates the cost of informal care for patients treated in advanced home care and analyses some patient characteristics that influence informal care costs.Methods: During one week in October 1995, data were collected on all 451 patients in advanced home care in the Swedish county of Östergötland. Costs were calculated by using two models: one including leisure time, and one excluding leisure time. Multiple regression analysis was used to analyze factors associated with costs of informal care.Results: Seventy percent of the patients in the study had informal care around the clock during the week investigated. The patients had, on average, five formal care visits per week, each of which lasted for almost half an hour. Thus, the cost of informal care constituted a considerable part of the cost of advanced home care. When the cost of leisure time was included, the cost of informal care was estimated at SEK 5,880 per week per patient, or twice as high as total formal caregiver costs. When leisure time was excluded, the cost of informal care was estimated at SEK 3,410 per week per patient, which is still 1.2 times higher than formal caregiver costs (estimated at SEK 2,810 per week per patient). Informal care costs were higher among patients who were men, who were younger, who had their own housing, and who were diagnosed with cancer.Conclusions: Studies of advanced home care that exclude the cost of informal care substantially underestimate the costs to society, regardless of whether or not the leisure time of the caregiver is included in the calculations.
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32

Liu, Huan. "Formal and Informal Care: Complementary or Substitutes in Care for Elderly People? Empirical Evidence From China." SAGE Open 11, no. 2 (April 2021): 215824402110164. http://dx.doi.org/10.1177/21582440211016413.

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To integrate the care resources of the elderly, while promoting the development of formal social care resources, some countries have gradually turned to the development of family informal care resources. In China, informal family care has a more important role, whereas social formal care resources are far from meeting the needs of older people. Thus, this strategy can only be effective if there is a clear complementary relationship between informal care and formal care. Empirical analysis is selected from the China Health and Nutrition Survey (CHNS) database, which conducted 10 follow-up surveys in 12 provinces and municipalities in China. A two-tier stochastic frontier (TSFA) model was used to analyze the relationship between three different kinds of formal care and informal family care. The formal complementary and substitute effects on informal care eventually led to higher actual informal care level. The net effect of formal care on informal care is positive, and the complementary effects of formal care are still dominant even in different regions. Increasing informal care does not crowd out or reduce formal care; thereby, facilitating the return of care to families can effectively reduce public service expenditures.
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33

Hlebec, Valentina. "Family Care Experience in a Decentralized Social Home Care Context." Lex localis - Journal of Local Self-Government 15, no. 3 (June 28, 2017): 495–511. http://dx.doi.org/10.4335/15.3.495-511(2017).

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This survey analyses the scope and intensity of informal care for the elderly residing in their homes in Slovenia and their determinants: the residing municipality of the care recipient, geographical distance between the informal carer and the care recipient, to the care recipients’ and the care givers’ individual characteristics. With the increasing private out-of-pocket financial contribution, which is determined by municipality, the scope and intensity of informal care shows a significant increase as shown by regression analysis. Inter-municipal cooperation and the introduction of gradual private financial contribution are proposed as tools for improving accessibility of social home care in Slovenia.
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34

JACOBS, MARIANNE, THEO VAN TILBURG, PETER GROENEWEGEN, and MARJOLEIN BROESE VAN GROENOU. "Linkages between informal and formal care-givers in home-care networks of frail older adults." Ageing and Society 36, no. 8 (June 15, 2015): 1604–24. http://dx.doi.org/10.1017/s0144686x15000598.

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ABSTRACTIn ageing societies, policy makers aim for more contact between informal and formal care-givers as it may enhance the quality of care. So far, the linkage between formal and informal care-givers is generally studied from a one-sided or a single dyadic perspective, without taking into account that care networks of community-dwelling older adults often exist of multiple informal and formal care-givers. The current study examines discussion of care between all potential informal–formal care-giver dyads in a care network, and relates this to characteristics of the older care recipient, the care network and the care-givers. Seventy-four Dutch older care recipients provided information on all care-givers who helped with five different types of tasks; 410 care-givers reported on the contact between all care-givers identified. Multi-level logistic regression was conducted in 2,150 informal–formal care-giver dyads and revealed that in 26 per cent of all these dyads discussion on care occurred. This was more likely when both care-givers performed multiple types of tasks, the informal care-giver was residing with the care recipient, and contact within the formal and the informal sub-network was higher. To enhance discussion of care between informal and formal care-givers in care networks where no discussion occurs at all, home-care organisations may need to allocate formal care-givers who form a bridge with an extra-residential care-giver of care recipients living alone.
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35

Penning, Margaret J., and Neena L. Chappell. "Self-Care in Relation to Informal and Formal Care." Ageing and Society 10, no. 1 (March 1990): 41–59. http://dx.doi.org/10.1017/s0144686x00007844.

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ABSTRACTThis paper examines the prevalence, inter-relationships and correlates of various forms of self, informal and formal care. Analyses of data drawn from a random sample of 743 non-institutionalised elderly individuals living in Winnipeg, Manitoba reveal similarities as well as differences among the three types of care. Self- and formal care are somewhat similar, being positively related and having similar correlates. Nevertheless, substitutability as a consequence of medical scepticism is also evident. Both are unrelated to informal care. It is poor health in the form of functional disability and the availability of support through the marital relationship which are the strongest correlates of informal care. In contrast, health (chronic conditions and perceived health status) as well as beliefs in the efficacy of both preventative health behaviours and medical services are among the strongest correlates of self- and formal care.
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36

Groneck, Max. "Bequests and Informal Long-Term Care." Journal of Human Resources 52, no. 2 (March 8, 2016): 531–72. http://dx.doi.org/10.3368/jhr.52.2.1214-6839r1.

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37

Jimenez, Danielle, Francesca Falzarano, Amy Horowitz, Verena Cimarolli, and Jillian Minahan. "LONG-DISTANCE CAREGIVERS’ INFORMAL CARE NETWORKS." Innovation in Aging 3, Supplement_1 (November 2019): S557. http://dx.doi.org/10.1093/geroni/igz038.2059.

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Abstract The purpose of this study (N=304) was to examine the characteristics of LDCs’ informal caregiver (IC) network (Co-caregivers [Co-CG], other informal helpers) providing assistance to the care recipient (CR), and factors associated with more help received from ICs. The majority of LDCs in the sample reported working with at least one IC (81.9%) indicating the existence of a secondary care network. LDCs and Co-CGs were often siblings in comparison to other informal helpers that were more likely to be the CR’s friend. Results also show that CRs with children, living in the community, receiving no formal services, and lower levels of cognitive impairment receive more hours of help from ICs. In addition, more hours of help by ICs were associated with LDCs’ having higher scores of depression and anxiety, spending more hours per month helping the CR, and more frequent contact with CR. These seemingly discrepant findings are discussed.
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38

Christie, Juliette, G. Rush Smith, Gail M. Williamson, Charles E. Lance, Tamar E. Shovali, and Luciana C. Silva. "Quality of informal care is multidimensional." Rehabilitation Psychology 54, no. 2 (May 2009): 173–81. http://dx.doi.org/10.1037/a0015705.

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39

Chen, Lu, Na Zhao, Hongli Fan, and Peter C. Coyte. "Informal Care and Labor Market Outcomes." Research on Aging 39, no. 2 (August 3, 2016): 345–71. http://dx.doi.org/10.1177/0164027515611184.

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Data were used from the 1991–2009 China Health and Nutrition Survey to examine the influence of informal care on labor market outcomes for married women of working aged, with emphasis on caregiving intensity. After accounting for potential endogeneity between caregiving and labor force participation (LFP) through simultaneous equations modeling, caregivers who provided more than 15 or 20 hr of caregiving per week were 4.5–7.7% less likely to be LFPs. Intensive caregivers who remained working had significantly lower (4.97–7.20) weekly hours of work. The significant positive effect of informal care on LFP only existed in the rural sample, and these women also had much lower hours of work than their urban counterparts. Opportunities exist for policy interventions that target intensive caregivers in order to allow them to balance both work and caregiving.
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40

Abel, Emily K. "Informal Care for the Disabled Elderly." Research on Aging 12, no. 2 (June 1990): 139–57. http://dx.doi.org/10.1177/0164027590122001.

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41

Jette, Alan M., Sharon L. Tennstedt, and Laurence G. Branch. "Stability of Informal Long-Term Care." Journal of Aging and Health 4, no. 2 (May 1992): 193–211. http://dx.doi.org/10.1177/089826439200400203.

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42

Zechner, M. "INFORMAL CARERS IN THE CARE MARKETS." Innovation in Aging 1, suppl_1 (June 30, 2017): 814. http://dx.doi.org/10.1093/geroni/igx004.2940.

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43

Leigh, Andrew. "Informal care and labor market participation." Labour Economics 17, no. 1 (January 2010): 140–49. http://dx.doi.org/10.1016/j.labeco.2009.11.005.

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44

BUCHIGNANI, NORMAN, and CHRISTOPHER ARMSTRONG-ESTHER. "Informal care and older Native Canadians." Ageing and Society 19, no. 1 (January 1999): 3–32. http://dx.doi.org/10.1017/s0144686x99007254.

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The number and relative proportion of older Native people in Canada are both increasing rapidly. So also is a social problems discourse asserting that informal care of older Native people by family and kin is traditional, and highly appropriate today. However, neither this discourse nor previous research satisfactorily address the informal care requirements of older Native people nor the gendered implications that high levels of informal care provision may have for Native caregivers. Informal care is provided to Canada's non-Native elderly people primarily by resident wives and non-resident daughters, and secondarily by husbands and sons. Data from the pan-provincial Alberta Native Seniors Study demonstrate that Native people aged 50 or more have comparatively high overall care requirements. Older Native Albertans are poor, and make extensive use of some government income support programmes. They also make moderate use of medical services. Extensive dependence on informal care, institutional barriers and local service unavailability lead Native seniors to under-utilise other formal programmes aimed generically at the older provincial population. Native seniors are much more likely to live with kin than are other Canadians. Informal care appears equally available to older women and men, and is provided chiefly by resident daughters, sons and spouses, and by non-resident daughters, sisters and sons. Extensive elderly caregiving requirements may impose a growing, double burden on many, who are also providing care for dependent children. Without further support, current and future requirements may significantly limit the options of caregiving women and men.
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45

Vlachantoni, A., J. Robards, J. Falkingham, and M. Evandrou. "Trajectories of informal care and health." SSM - Population Health 2 (December 2016): 495–501. http://dx.doi.org/10.1016/j.ssmph.2016.05.009.

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Lichtendahl, Adinda. "Balancing between formal and informal care." Onderwijs en gezondheidszorg 35, no. 4 (June 2011): 28–30. http://dx.doi.org/10.1007/s12477-011-0048-1.

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Barmby, Tim, and Sue Charles. "INFORMAL CARE AND FEMALE LABOUR SUPPLY." Scottish Journal of Political Economy 39, no. 3 (August 1992): 288–301. http://dx.doi.org/10.1111/j.1467-9485.1992.tb00622.x.

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Harding, Richard. "Informal caregivers in home palliative care." Progress in Palliative Care 21, no. 4 (September 2013): 229–31. http://dx.doi.org/10.1179/1743291x13y.0000000056.

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Hall, Jane, Patricia Kenny, Ishrat Hossain, Deborah J. Street, and Stephanie A. Knox. "Providing Informal Care in Terminal Illness." Medical Decision Making 34, no. 6 (August 13, 2013): 731–45. http://dx.doi.org/10.1177/0272989x13500719.

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Kim, Hyuncheol Bryant, and Wilfredo Lim. "Long-term care insurance, informal care, and medical expenditures." Journal of Public Economics 125 (May 2015): 128–42. http://dx.doi.org/10.1016/j.jpubeco.2014.12.004.

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