Citations (34)
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Abiola O. Keller, Nia C. Norris, Bashir Easter, Andrea Garr, Gail Morgan, Ramona Dicks-Williams & Colleen Galambos. (2023) A time for me: A virtual program to engage African American caregivers. Journal of Women & Aging 35:4, pages 369-382.
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Mingming Xu & Wei Yang. (2023) Depressive symptoms among older empty nesters in China: the moderating effects of social contact and contact with one’s children. Aging & Mental Health 27:1, pages 54-69.
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Chelsea Liu, Victoria R. Marino, Virginia J. Howard, William E. Haley & David L. Roth. (2023) Positive aspects of caregiving in incident and long-term caregivers: Role of social engagement and distress. Aging & Mental Health 27:1, pages 87-93.
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Josefine Antoniades, Samantha Croy, Andrew Simon Gilbert, Antonia Thodis, Carolina Navarro Medel, Phuong Lan Do, Thu Ha Dang, Mike Kent & Professor Bianca Brijnath. (2022) Focused Attention on Positive Aspects of Dementia Care in Culturally and Linguistically Diverse Communities: Qualitative Insights from Australia. Clinical Gerontologist 0:0, pages 1-12.
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Kirsten Jæger Fjetland & Miroslava Tokovska. (2022) What characterizes studies on social support groups for next of kin of persons with dementia? A qualitative systematic review. Nordic Social Work Research 12:4, pages 464-479.
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Hanan AboJabel & Perla Werner. (2022) The mediating effect of social support and coping strategies on the relation between family stigma and caregiver burden among Israeli Arab family caregivers of people with Alzheimer’s disease (AD). Aging & Mental Health 26:8, pages 1597-1603.
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Jennifer L. Bevan, Tessa Urbanovich & Maya Vahid. (2021) Family Communication Patterns, Received Social Support, and Perceived Quality of Care in the Family Caregiving Context. Western Journal of Communication 85:1, pages 83-103.
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Christine Unson, Deborah Flynn, Queendalene Chukwurah, Mary Anne Glendon & Tammy Testut. (2020) Uncertainty in Transition of African American Caregivers. Issues in Mental Health Nursing 41:5, pages 445-454.
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Nicole B. Haverstock, Joelle C. Ruthig & Judith G. Chipperfield. (2020) Primary and secondary control strategies and psychological well-being among familial caregivers of older adults with dementia. The Journal of Social Psychology 160:1, pages 61-74.
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Jennifer C. Greenfield, Leslie Hasche, Lauren M. Bell & Heidi Johnson. (2018) Exploring how workplace and social policies relate to caregivers’ financial strain. Journal of Gerontological Social Work 61:8, pages 849-866.
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Steven H. Zarit. (2018) Past is prologue: how to advance caregiver interventions. Aging & Mental Health 22:6, pages 717-722.
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Articles from other publishers (23)
Kalisha Bonds Johnson, Melinda Higgins, Fayron Epps, Glenna S Brewster, Karah Alexander & Kenneth Hepburn. (2023) Tele-Savvy Outcomes of Non-Hispanic Black American and White Caregivers. The Gerontologist.
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Tiffany B Kindratt, Dominique L Sylvers, Aya Yoshikawa, Mónika López-Anuarbe, Noah J Webster & Erin D Bouldin. (2023) Dementia Caregiving Experiences and Health Across Geographic Contexts by Race and Ethnicity. The Journals of Gerontology: Series B 78:Supplement_1, pages S48-S58.
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Yan-Ru Lin, Hsiu-Li Huang & Chien-Liang Liu. (2022) Factors associated with positive aspects of caregiving experiences among family caregivers of persons living with dementia in Taiwan: A cross-sectional study. Geriatric Nursing 48, pages 229-236.
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Yeonjung Lee & Lun Li. (2022) Evaluating the Positive Experience of Caregiving: A Systematic Review of the Positive Aspects of Caregiving Scale. The Gerontologist 62:9, pages e493-e507.
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Alexa Dessy, Amanda J. Zhao, Kay Kyaw, Dorice Vieira & Joel Salinas. (2022) Non-Pharmacologic Interventions for Hispanic Caregivers of Persons with Dementia: Systematic Review and Meta-Analysis. Journal of Alzheimer's Disease 89:3, pages 769-788.
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Mahaveer Golechha, Tasneem Bohra, Mehul Patel & Sonalini Khetrapal. (2021) Healthcare worker resilience during the COVID‐19 pandemic: A qualitative study of primary care providers in India. World Medical & Health Policy 14:1, pages 6-18.
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Carol Ann Podgorski, Sharon D. Anderson & Jasneet Parmar. (2021) A Biopsychosocial-Ecological Framework for Family-Framed Dementia Care. Frontiers in Psychiatry 12.
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Chelsea Liu, Adrian N S Badana, Julia Burgdorf, Chanee D Fabius, David L Roth & William E Haley. (2021) Systematic Review and Meta-Analysis of Racial and Ethnic Differences in Dementia Caregivers’ Well-Being. The Gerontologist 61:5, pages e228-e243.
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Nader Mehri, Jennifer Kinney, Scott Brown & Mahdie Rajabi Rostami. (2019) Informal Caregiving and All-Cause Mortality: A Meta-Analysis of Longitudinal Population-Based Studies. Journal of Applied Gerontology 40:7, pages 781-791.
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Michael J. McCarthy, Morgan Lee-Regalado Hustead, Rachel Bacon, Y. Evie Garcia, Dorothy J. Dunn, Heather J. Williamson & Julie Baldwin. (2021) Development and Validation of a Community Assessment Survey for Diverse Rural Family Caregivers of People With Alzheimer Disease and Related Dementias. Family & Community Health 44:3, pages 126-135.
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Heather J Williamson, Michael J McCarthy, Yolanda E Garcia, Rachel Bacon, Dorothy J Dunn & Julie A Baldwin. (2020) Addressing the Needs of Rural Caregivers of Individuals With Alzheimer’s Disease and Related Dementias During and Beyond Coronavirus Disease 2019 (COVID-19). Public Policy & Aging Report 30:4, pages 178-180.
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Fiona Devi, Qi Yuan, Peizhi Wang, Gregory Tee Hng Tan, Richard Roshan Goveas, Li Ling Ng, Siow Ann Chong & Mythily Subramaniam. (2020) Positive aspect of caregiving among primary informal dementia caregivers in Singapore. PLOS ONE 15:8, pages e0237677.
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Oscar Ribeiro, Daniela Brandão, Ana F. Oliveira, Laetitia Teixeira & Constança Paúl. (2019) Positive aspects of care in informal caregivers of community‐dwelling dementia patients. Journal of Psychiatric and Mental Health Nursing 27:4, pages 330-341.
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V. C. Tatzer, E. Reitinger, P. Plunger & K. Heimerl. (2019) „Wenn es nicht schlimmer wird, kann ich damit leben“ Bedürfnisse und Erfahrungen pflegender Angehöriger von Menschen mit Demenz in Österreich“I can live with it, if it doesn’t get worse”—Caregivers of people with dementia in Austria talk about their needs and experiences. Zeitschrift für Gerontologie und Geriatrie 53:3, pages 245-250.
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Perla Werner & Hanan AboJabel. (2018) Can drawings help assessing dementia caregivers' burden? A preliminary study. Dementia 19:3, pages 661-675.
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Deborah Carr & Rebecca L. Utz. (2020) Families in Later Life: A Decade in Review. Journal of Marriage and Family 82:1, pages 346-363.
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Alexandra Rae Hodson, Shelley Peacock & Lorraine Holtslander. (2019) Family caregiving for persons with advanced heart failure: An integrative review. Palliative and Supportive Care 17:6, pages 720-734.
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Naoko Muramatsu & Lijuan Yin. (2019) Gentle Physical Activity Intervention Led by Caregivers in a Medicaid Home Care Program: Do Outcomes Differ Between Family and Nonfamily Caregiving Dyads?. Innovation in Aging 3:3.
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Fayron Epps, Karen M. Rose & Ruth Palan Lopez. (2019) Who's Your Family?: African American Caregivers of Older Adults With Dementia. Research in Gerontological Nursing 12:1, pages 20-26.
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Marie-Conception Leocadie, Marie-Hélène Roy & Monique Rothan-Tondeur. (2018) Barriers and enablers in the use of respite interventions by caregivers of people with dementia: an integrative review. Archives of Public Health 76:1.
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Kohei Kajiwara, Hiroko Noto & Makoto Yamanaka. (2018) Changes in caregiving appraisal among family caregivers of persons with dementia: A longitudinal study over 12 months. Psychogeriatrics 18:6, pages 460-467.
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Leisa Easom, Ellen Cotter & Angel Ramos. (2018) Comparison of African American and Caucasian Caregiver Self-Efficacy. Journal of Gerontological Nursing 44:3, pages 16-21.
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Petra Plunger, Verena C. Tatzer & Katharina Heimerl. 2018. Alter und Geschlecht. Alter und Geschlecht
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