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Gotowe bibliografie tematyczne / Caregivers

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Gotowa bibliografia na temat „Caregivers”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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Artykuły w czasopismach na temat "Caregivers"

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Savla, Jyoti, Karen Roberto, and Rosemary Blieszner. "CARE NETWORKS OF RURAL APPALACHIAN FAMILY CAREGIVERS AND PERSONS LIVING WITH DEMENTIA." Innovation in Aging 6, Supplement_1 (2022): 194. http://dx.doi.org/10.1093/geroni/igac059.776.

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Abstract Dementia care research typically focuses on primary family caregivers with limited consideration of their engagement with a broader care network and the geographic area in which they reside. Using a mixed-methods approach, we analyzed care networks of 163 primary caregivers and their relative living with dementia in rural Virginia. Six distinct care network types emerged based on the primary caregiver's gender, relationship to the person living with dementia, and presence of other informal caregivers. Networks differed by the caregiver’s emotional connectivity with family/friends and

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Buchanan, Robert J., and Chunfeng Huang. "The Need for Mental Health Care Among Informal Caregivers Assisting People with Multiple Sclerosis." International Journal of MS Care 15, no. 2 (2013): 56–64. http://dx.doi.org/10.7224/1537-2073.2012-030.

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The objective of this study was to identify characteristics of informal caregivers and people with multiple sclerosis (MS) receiving assistance that are associated with the caregiver's perceived need for mental health care. Survey data were collected in interviews with 530 caregivers and analyzed using a logistic regression model. We found that older caregiver age significantly decreased the odds of caregivers' perceived need for mental health treatment. Better mental health domains of health-related quality of life among caregivers, as measured by the 8-item Short Form Health Status Survey (S

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Messias, Lisiane Alves dos Santos, Fátima Adriana D'Almeida Gazetta, Pedro Marco Karan Barbosa, and Zamir Calamita. "Conhecimento prático e sobrecarga na vida de cuidadores de idosos com demência." Scientia Medica 28, no. 3 (2018): 30569. http://dx.doi.org/10.15448/1980-6108.2018.3.30569.

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AIMS: To analyze the level of knowledge and the life overload of caregivers of elderly people with dementia, correlating these variables with sociodemographic aspects and type of relationship between caregiver and elderly.METHODS: A cross-sectional study was conducted between 2016 and 2017, with caregivers of elderly people with dementia seen at the Geriatrics outpatient clinic of the Hospital das Clínicas, Medical School of Marília, in Marília / SP, Brazil. The study included caregivers who accompanied the elderly to the consultations and participated in an important way in their care, compri

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Frias, Cindy E., Esther Cabrera, and Adelaida Zabalegui. "Informal Caregivers’ Roles in Dementia: The Impact on Their Quality of Life." Life 10, no. 11 (2020): 251. http://dx.doi.org/10.3390/life10110251.

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The constantly changing process of caring for a person with dementia affects the informal caregivers’ role due to its psychosocial impact. This cross-sectional study aimed to analyze the impact of the Person with Dementia informal caregiver’s role caregiver to a person with dementia on the self-perceived quality of life (QoL) of the caregiver. In total, 160 informal caregivers were recruited between January and December 2019. Informal caregivers’ quality of life was assessed using the European Quality of Life 5-Dimension scale, burden with the Zarit Burden Scale, emotional wellbeing using the

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Angelika, Putu Veby, The Maria Meiwati Widagdo, Widya Christine Manus, and Silvester Haripurnomo. "CORRELATION STUDY BETWEEN BURDENS AND THE QUALITY OF LIFE IN CAREGIVERS OF DEPENDENT ELDERLY IN PRAWIRODIRJAN VILLAGE." Journal of Widya Medika Junior 4, no. 2 (2022): 114–24. http://dx.doi.org/10.33508/jwmj.v4i2.3779.

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Background: Aging is synonymous with decreased body function due to natural factors (aging process) and diseases. The elderly who are unable to do their activities can cause dependence on the caregiver. In carrying out its role, the caregiver has burdens that can affect their life quality. Objective: To measure the correlation between the burden and the quality of life in caregivers of dependent elderly in Prawirodirjan Sub-district, Gondomanan District, Yogyakarta Municipality. Materials and Methods: This study used a cross-sectional method with a total sample of 33 participants. Caregiver bu

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Yousaf, Aiza, Hira Iqbal, Rabeea Zubair, Muhammad Kashif, Danish Hassan, and Rizwan Ahmed. "Factors associated with caregiver burden among caregivers of cerebral palsy children." Professional Medical Journal 27, no. 08 (2020): 1555–59. http://dx.doi.org/10.29309/tpmj/2020.27.08.3781.

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Cerebral palsy(CP) is the term for a group of brain disorders, caused by damage to parts of the developing brain that control muscle movement, balance, and posture before birth, during birth, or immediately after birth. Caregivers of children with CP often experience high levels of caregiving burden. Objectives: The aim of this study was to explore correlation of factors with the presence of burden on primary caregivers of CP children. Study Design: Cross-Sectional study. Setting: Department of Physiotherapy, Children Hospital, Lahore. Period: March 2017 to June 2017. Material & Methods: W

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Chou, Yueh-Ching, Li-yeh Fu, Li-Chan Lin, and Yue-Chune Lee. "Predictors of subjective and objective caregiving burden in older female caregivers of adults with intellectual disabilities." International Psychogeriatrics 23, no. 4 (2010): 562–72. http://dx.doi.org/10.1017/s1041610210001225.

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ABSTRACTBackground: Informal, unpaid, and lifelong older caregivers of adults with intellectual disabilities (ID) are usually female and most often are mothers of adults with ID. However, research exploring different predictors of subjective and objective burden among these older female caregivers is sparse. The objective of this study was to examine whether the subjective and objective burden as well as positive appraisals are predicted by the same or different variables linked to the caregivers and the adults with ID.Methods: Face-to-face interview questionnaires were administered in a city

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Krishnan, Shilpa, Haobin Tony Chen, Sarah Caston, and Seunghwa Rho. "Physical and Psychological Burden among Caregivers of Latinx Older Adults with Stroke and Multimorbidity." Ethnicity & Disease 33, no. 4 (2023): 156–62. http://dx.doi.org/10.18865/ed.33.4.156.

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Objective To investigate the association between Latinx older adults’ stroke, multimorbidity, and caregiver burden. Methods For this retrospective cohort study, we used the Hispanic Established Populations for the Epidemiologic Study of the Elderly (H-EPESE) Wave-7 data set. The caregiver’s physical burden was defined by using the Level of Burden Index. The caregiver’s psychological burden was measured by using the Perceived Stress Scale (PSS-4). Multimorbidity was defined as the presence of 3 or more chronic conditions. Results The average age of the Latinx adults was 86 years, and the caregi

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Braun, Michal, Mario Mikulincer, Anne Rydall, Andrew Walsh, and Gary Rodin. "Hidden Morbidity in Cancer: Spouse Caregivers." Journal of Clinical Oncology 25, no. 30 (2007): 4829–34. http://dx.doi.org/10.1200/jco.2006.10.0909.

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Purpose This study assesses psychological distress among advanced cancer patients and their spouse caregivers, while examining the relative contribution of caregiving burden and relational variables (attachment orientation and marital satisfaction) to depressive symptoms in the spouse caregivers. Methods A total of 101 patients with advanced GI or lung cancer and their spouse caregivers were recruited for the study. Measures included Beck Depression Inventory–II (BDI-II), Caregiving Burden scale, Experiences in Close Relationships scale, and ENRICH Marital Satisfaction scale. Results A total o

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Grivel, Charlotte, Pierre Nizet, Manon Martin, et al. "The experience of being a caregiver of patients with digestive cancer, from patients and caregivers’ perception: A mixed study." PLOS ONE 18, no. 7 (2023): e0287335. http://dx.doi.org/10.1371/journal.pone.0287335.

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Backgrounds Caregivers are essential in the care of a patient with digestive cancer. Considering their experience and needs is crucial. Objectives To explore the experience of caregivers of patients with digestive cancer and to compare the perspectives of patients and caregivers. Methods A mixed-methods study with a cross-sectional prospective and a comprehensive qualitative dimension was performed in a medical oncology unit in a French tertiary hospital. Dyads made of patients with digestive cancer and their caregiver were recruited. The Caregiver Reaction Assessment (CRA) and the Supportive

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Rozprawy doktorskie na temat "Caregivers"

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Kaushik, Sanjana. "Social Networks of Technology Caregivers and Caregivees." University of Cincinnati / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1613749933487134.

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Nauser, Julie Ann. "Heart failure family caregivers psychometrics of a new quality of life scale and variables associated with caregiver outcomes /." Connect to resource online, 2007. http://hdl.handle.net/1805/1139.

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Thesis (Ph.D.)--Indiana University, 2007.<br>Title from screen (viewed on September 21, 2007). School of Nursing, Indiana University-Purdue University Indianapolis (IUPUI). Advisor(s): Tamilyn Bakas, Sharon Sims, Mary L. Fisher, Janet Welch. Includes vitae. Includes bibliographical references (leaves 228-244).

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Kum, Cleopatra Eghem. "Theoretically Based Factors Affecting Health in Stroke Family Caregivers." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1627660913055465.

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Kimemia, Veronica. "CAREGIVER BURDEN AND COPING RESPONSES FOR FEMALES WHO ARE THE PRIMARY CAREGIVER FOR A FAMILY MEMBER LIVING WITH HIV/AIDS IN KENY." Doctoral diss., University of Central Florida, 2006. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/2682.

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Caring for a family member who is ill can be a draining experience (Cooper et al., 2006; Daire, 2002; Zarit et al, 1980). Providing care for a family member that is living with HIV/AIDS is potentially even more stressful because of social meanings associated with HIV/AIDS infection (Stajduhar, 1998) and the contagious nature of the HIV virus (Powell-Cope & Brown, 1992). Research indicates that most caregivers are female (Bunting, 2001; Songwathana, 2000). In Africa women bear the brunt of the burden of providing care for family members who are living with HIV/AIDS (Mushonga, 2001; Olenja, 1999

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Demirtepe, Dilek. "Testing The Caregiver Stress Model With The Caregivers Of Children With Leukemia." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/12609327/index.pdf.

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The aim of the present study was to investigate the relationship between the stressors of the caregiving process and the health related outcomes (depression, anxiety, and general psychological health) in caregivers of children with leukemia. Caregiver Stress Model was used as the conceptual framework for the study. In order to measure the stressors of the caregivers, caregiver well-being scale was adapted to Turkish culture as the study 1 by using the caregivers of family members with various chronic illnesses. The analyses showed that Turkish version of the caregiver well-being scale had sati

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Konag, Ozlem. "Testing The Caregiver Stress Model With The Primary Caregivers Of Schizophrenic Patients." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613797/index.pdf.

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The aim of this study was to examine the relationship between the stressors of caregiving for a schizophrenic patient and related outcomes. The Caregiver Stress Model was used as the conceptual framework for the current study. The sample of the study was composed of 98 Turkish caregivers of schizophrenic patients who were treated at psychiatry clinics of hospitals in Ankara. Twelve mediation models were tested using marital satisfaction and social support as mediators. The models contained primary stressor (basic needs), secondary stressor (activities of living), and intrapsychic strain (paren

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Coolbear, Jennifer. "Caregiver-infant interactions and caregivers' representations of relationships in failure to thrive." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ56222.pdf.

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Salinas, Maureen R. "Caregiver Burden and Depressive Symptoms in Hispanic Caregivers of Alzheimer's Disease Patients." Scholarship @ Claremont, 2016. http://scholarship.claremont.edu/scripps_theses/795.

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Caregiving for a close family member with Alzheimer’s disease is a stressful situation to be in, that often leads to high levels of caregiver burden and subsequent stress and depressive symptoms, and while there are numerous community and government resources available to caregivers, there are aspects of Hispanic cultures that may lead Hispanic caregivers to have higher levels of caregiver burden and depressive symptoms than White caregivers. 80 Hispanic caregivers and 80 White caregivers, with 40 males and 40 females within each group, will be recruited to participate in this study. Scales wi

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King, Jennifer Kay. "Caregiving Style in Diverse Samples of Caregivers." Thesis, University of North Texas, 2006. https://digital.library.unt.edu/ark:/67531/metadc5363/.

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With three homogenous caregiver groups (i.e., Alzheimer's caregivers, grandparents raising grandchildren, parents), caregiving styles were explored to determine their reliability and validity, their unique role in predicting caregiver outcomes, and their differences between groups of caregivers. A conceptual framework was adapted to determine the impact of contextual variables, caregiving styles, caregiver appraisal, and mediating variables on caregiving outcomes. A more concise version of the Caregiving Style Scale (CSS) was developed with 49 items yielding an internal consistency coefficient

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Patel, Bina Ranjit. "A Mixed Methods Inquiry of Caregivers of Veterans with Sustained Serious "Invisible" Injuries in Iraq and/or Afghanistan." Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6562.

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Currently, there are approximately 1.1 million caregivers who are caring for veterans who have served in the military following September 11 (9/11), 2001 (Ramchand et al., 2014). In this study, a mixed methods analysis of post 9/11 caregivers enrolled in the North Florida South Georgia Caregiver Support Program was completed with a convenience sample of 172 participants for quantitative analysis which included 16 participants for the phenomenological query. Correlations, t-tests, and ANOVAs were used to determine the associations among race, gender, age, caregiver type, diagnosis, tier level,

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Książki na temat "Caregivers"

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Duncan, Boyd Marlyn, and Hale Janet Fraser, eds. The caregiver's guide: For caregivers and the elderly. Nelson-Hall, 1992.

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Elliot, Linda K. Growing great kids for child caregivers: Child caregiver curriculum. Great Kids, 2002.

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Sheehan, Pauline J. Hugs for caregivers. WinePress Pub., 1998.

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Arizona. Aging and Adult Administration and United States. Administration on Aging, eds. Volunteer caregivers program. Arizona Dept. of Economic Security, Aging and Adult Administration, 1992.

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Schonhoff, Shelly. Family caregivers guide. Simon & Kolz Pub., 1998.

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J, Kramer Betty, and Thompson Edward H, eds. Men as caregivers. Prometheus Books, 2005.

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Boulden, Jim. The caregivers handbook. J. Boulden, 1991.

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Navarra, Tova. Wisdom for caregivers. Slack, Inc., 1995.

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1936-, Moroney Robert, and Davis Pam, eds. Caring & competent caregivers. University of Georgia Press, 1998.

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Gates, Katherine, book designer, editor, ed. Cartoons for caregivers. River Inkers, 2013.

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Części książek na temat "Caregivers"

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Abrams, David B., J. Rick Turner, Linda C. Baumann, et al. "Alzheimer's Caregivers." In Encyclopedia of Behavioral Medicine. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1005-9_100063.

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Zarit, Steven H., and Courtney A. Polenick. "Caregivers’ Outcomes." In Encyclopedia of Gerontology and Population Aging. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-69892-2_8-1.

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Yan, Elsie. "Primary Caregivers." In Encyclopedia of Gerontology and Population Aging. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-69892-2_851-1.

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Marbach, Christina. "Young Caregivers." In Encyclopedia of Child Behavior and Development. Springer US, 2011. http://dx.doi.org/10.1007/978-0-387-79061-9_3147.

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Parker, Gordon, Gabriela Tavella, and Kerrie Eyers. "Forgotten caregivers." In Burnout. Routledge, 2022. http://dx.doi.org/10.4324/9781003333722-14.

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Ferrell, Betty R., and Polly Mazanec. "Family Caregivers." In Geriatric Oncology. Springer US, 2009. http://dx.doi.org/10.1007/978-0-387-89070-8_7.

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Perper, Joshua A., and Stephen J. Cina. "Contagious Caregivers." In When Doctors Kill. Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-1369-2_19.

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Siskowski, Connie. "Adolescent caregivers." In How caregiving affects development: Psychological implications for child, adolescent, and adult caregivers. American Psychological Association, 2009. http://dx.doi.org/10.1037/11849-002.

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Zarit, Steven H., and Courtney A. Polenick. "Caregivers’ Outcomes." In Encyclopedia of Gerontology and Population Aging. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-22009-9_8.

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Yan, Elsie. "Primary Caregivers." In Encyclopedia of Gerontology and Population Aging. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-22009-9_851.

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Streszczenia konferencji na temat "Caregivers"

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Pasternak, Logan, Srijohn Roy, Andrew Farag, Monica Rubens, Ameek Chadha, and Sasan Haghani. "IoT Mobile Application for Alzheimer's Disease Caregivers." In 2025 IEEE International Conference on Consumer Electronics (ICCE). IEEE, 2025. https://doi.org/10.1109/icce63647.2025.10929805.

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Naswa, Raghav, Sugam Jaiswal, Remya Mavila, Weichao Yuwen, Bill Erdly, and Dong Si. "Assessing Empathy in Mental Health Caregivers using Conversational AI." In 2024 IEEE 12th International Conference on Healthcare Informatics (ICHI). IEEE, 2024. http://dx.doi.org/10.1109/ichi61247.2024.00079.

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Gerassi, Renata, Larissa de Andrade, Maria Candanedo, Carolina Tsen, Décio Neto, and Juliana Ansai. "CAREGIVER SATISFACTION FOR TELEREHABILITATION AND FOLLOW-UP INTERVENTION FOR ELDERLY FAMILIES WITH DEMENTIA." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda075.

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Background: Understanding the satisfaction with telerehabilitation as a positive evaluation of the individual about the service offered, this is a fundamental aspect to measure the quality of care and the relevance of these services provided. Objective: Compare the caregiver’s satisfaction to a telerehabilitation program and to a remote follow-up for families of elderly people with dementia. Methods: Randomized clinical trial, with blinding of the evaluator, controlled by two groups: Intervention (IG) and Control (CG). In the initial assessment, 10 caregivers of elderly people with dementia we

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Cendrasilvinia, Herose, The Maria Meiwati Widagdo, and Widya Christine Manus. "Burden and Quality of Life of Dependent Elderly Caregivers in Pakuncen Village Yogyakarta." In The 7th International Conference on Public Health 2020. Masters Program in Public Health, Universitas Sebelas Maret, 2020. http://dx.doi.org/10.26911/the7thicph.01.08.

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Background: Elderly people face health problems associated with reduced health and increased disability. Dependent elderly on caregivers who cause a burden affecting the quality of life of caregivers. The aim of this study was to analyze the correlation between the burden and quality of life among dependent elderly caregivers. Subjects and Method: A cross-sectional study was carried out in Pakuncen Village, Yogyakarta. The study subjects were 30 informal caregivers who cared for their family member aged ≥ 60 years with moderate dependence. Instruments used to screen dependent elderly included

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Pappachen, Nikitha, and Maithri Goud. "Relationship Between Caregiver Burden and Socioeconomic Status." In 28th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2024. http://dx.doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.176_2024.

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In this study, caregiver burden measures the psychosocial strain a caregiver experiences as a result of caring for a person with autism. In addition, this study focuses on the effect of socioeconomic status on caregiver burden. A previous study found an association between lower primary caregiver education level and more sleep problems for children with autism3. Thus, the finding focuses on the child with autism as opposed to the caregiver burden. Other studies focus on elements that affect caregiver burden such as sleep quality, mental health, and cultural aspects. If it is known that socioec

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Mathew, Brian Joseph, Maduka Gunasinghe, Usmaan Al-Shehab, Samrat Gollapudi, Prince Patel, and Maithri Goud. "Factors Affecting Caregiver Burden in Informal Caregivers of Patients with Autism Spectrum Disorder." In 28th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2024. http://dx.doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.188_2024.

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Individuals with Autism Spectrum Disorder (ASD) often require lifelong care to meet their daily needs, which is typically provided by informal sources like family members as well as formal caregivers from home health agencies. The persistent stress of raising a child with ASD can potentially lead to parental burnout, highlighting the importance of understanding the struggles faced by these caregivers. Clinicians must prioritize the well-being of both the individuals with ASD and their dedicated caregivers by gaining a comprehensive understanding of the challenges they encounter. Our research a

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Gunasinghe, Maduka, Krisha S. Patel, Usmaan Al-Shehab, Brian Joseph Mathew, Maithri Goud, and Andrea Iannuzzelli. "Variables Contributing to The Psychosocial Strain on Caregivers of Patients with Autism Spectrum Disorder." In 28th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2024. https://doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.57_2024.

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This research, conducted at the Rowan-Virtua Integrated Special Needs (RISN) Center, Sewell, New Jersey, explores the psychosocial strain on caregivers of patients with Autism Spectrum Disorder (ASD). Utilizing the Caregiver Burden Inventory (CBI), we assessed multiple psychosocial dimensions, including time dependency, emotional health, development, social relationships, and physical health. Data was extracted from a total of 295 patient charts; this poster analyzes the initial sample of 99 patients by incorporating demographic variables and caregiver burden scores into a tailored database fo

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Asano, Katsuhiro, Shinichiro Ota, and Jinro Takato. "Evaluation of Power-Assisted Wheelchair to Reduce Burden on Elderly Caregivers." In ASME 2023 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/imece2023-112498.

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Abstract The purpose of this study is to verify the effectiveness of a mechanical power-assisted wheelchair that does not require electrical charging for its operation. In this study, we investigated the burden experiences by a caregiver when pushing the wheelchair along with the assistive force with and without the power assistance. First, the wheelchair was tested on a slope where the caregiver would feel strain while pushing the wheelchair, and the wheelchair pushing force and sensory evaluation were measured. The results showed that the caregiver’s pushing force was independent of the impl

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Moreira, Verônica, Valquiria Nedel, Márcia Lorena Chaves, Raphael Castilhos, and Maira Olchik. "DYSPHAGIA ASSOCIATED CAREGIVER BURDEN IN ALZHEIMER DISEASE." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda047.

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Background: Dysphagia is prevalent in Alzheimer’s disease (AD) and can influence caregivers’ burden. Objectives: Evaluate the impact of feeding process in caregivers’ burden of individuals with AD. Methods: This is a cross-sectional study. Caregivers of individuals with AD who attended the dementia outpatient clinic and are over 18 years of age were included. We collected demographic variables and the Zarit Burden Interview - Short Version (ranging from 0 to 48) and The Edinburgh Feeding Evaluation in Dementia Scale (scoring from 0 to 20) scales. Relationship between the two scales and demogra

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Gustafson, Kimberly, William Durfee, Gregory Voss, Andrew Hansen, and Gary Goldish. "A LIGHTWEIGHT, FOLDABLE MOTORIZED TRANSPORT CHAIR TO EASE CAREGIVER BURDEN." In 2023 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/dmd2023-6138.

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Abstract As the population ages, the number of caregivers in the Unites States is growing rapidly. The burden on these caregivers is exacerbated by steadily increasing obesity rates, which are highest in adults aged 50 to 70. The Caregiver-Assist Transport Chair (CATC) is designed to address the difficulty many caregivers experience assisting in the transportation of moderate to low mobility care recipients outside of the home for appointments, community engagements, or fresh air excursions. It is not uncommon for the caregiver to be elderly or of a smaller build than the care recipient, incre

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Raporty organizacyjne na temat "Caregivers"

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Raimondi, Alessandra. Oklahoma Caregivers Support a Family Caregiver Tax Credit. AARP Research, 2023. http://dx.doi.org/10.26419/res.00597.001.

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Wu, Huijing. Coresident Grandparents: Caregivers versus Non-Caregivers. National Center for Family & Marriage Research, 2018. http://dx.doi.org/10.25035/ncfmr/fp-18-02.

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DiAngelo, Lucy, Libby Lowry, Kayla McDaniel, Clare Sauser, Shelby Terry, and Erin Williams. Increasing Confidence and Mental Health in Caregivers. University of Tennessee Health Science Center, 2021. http://dx.doi.org/10.21007/chp.mot2.2021.0011.

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The purpose of our critically appraised topic is to synthesize the highest-level evidence available regarding interventions for increasing confidence and mental health outcomes in caregivers taking loved ones home from inpatient rehabilitation. The final portfolio contains six research articles from peer-reviewed journals. Study designs include randomized control trials, a systematic review, and a pretest-posttest without a control group. All studies relate directly to the components of the PICO question. Four of the articles discussed both caregiver confidence and mental health while two arti

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Baker-Henningham, Helen, Francis Taja, and Marsha Bowers. A Mixed-method Feasibility Trial of an Early Childhood, Violence Prevention, Parenting Program Integrated into Preschool Provision in Jamaica. Inter-American Development Bank, 2025. https://doi.org/10.18235/0013518.

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We adapted a violence-prevention, parenting program (the Irie Homes Toolbox, or IHT) for integration into Jamaican preschool services. The adapted IHT was evaluated in a mixed-method feasibility trial in Kingston, Jamaica. Twenty-four preschools were randomly assigned to intervention (n12) or wait-list control (n12). Ten caregivers per school were recruited (n240, n120/group). The program consisted of eleven 1-hour parenting sessions delivered by a preschool teacher with groups of ten caregivers of children aged 2-6 years. In the impact evaluation, the primary outcome was caregivers' use of vi

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Guengerich, Terri. Support Family Caregivers: Support a Family Caregiver State Income Tax Credit: Infographic. AARP Research, 2019. http://dx.doi.org/10.26419/res.00259.090.

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Oliveira, Lélia, Larissa Pedreira, Ana Paula Jesus, et al. Hospital-home transitional care and support for home caregivers of elderly people with functional dependence: a scoping review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.3.0143.

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Review question / Objective: The review questions of this scoping are: 1. How does hospital-home transitional care support home caregivers of functionally dependent elderly people? 2. How is hospital-home transitional care applied to support home caregivers of elderly people with functional dependence? 3. What experiences of transitional hospital-home care were successful in supporting home caregivers of elderly people with functional dependence? The objective of this scoping review is to identify the hospital-home transitional care offered as support to the home caregiver of elderly people wi

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Squiers, Linda, Mariam Siddiqui, Ishu Kataria, et al. Perceived, Experienced, and Internalized Cancer Stigma: Perspectives of Cancer Patients and Caregivers in India. RTI Press, 2021. http://dx.doi.org/10.3768/rtipress.2021.rr.0044.2104.

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Cancer stigma may lead to delayed diagnosis and treatment, especially in low- and middle-income countries. This exploratory, pilot study was conducted in India to explore the degree to which cancer stigma is perceived, experienced, and internalized among adults living with cancer and their primary caregivers. We conducted a survey of cancer patients and their caregivers in two Indian cities. The survey assessed perceived, experienced, and internalized stigma; demographic characteristics; patient cancer history; mental health; and social support. A purposive sample of 20 cancer survivor and car

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David, Patty, and Colette Thayer. Who Are Today's Caregivers? AARP Research, 2020. http://dx.doi.org/10.26419/res.00391.003.

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Kakulla, Brittne. Technology Trends Among Caregivers. AARP Research, 2023. http://dx.doi.org/10.26419/res.00584.014.

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Raimondi, Alessandra, and Vicki Levy. Caregivers Find Travel Rewarding. AARP Research, 2024. http://dx.doi.org/10.26419/res.00804.003.

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