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Understanding the Needs of Caregivers

Caregiver identity theory and predictors of burden and depression: Findings from the REACH II study

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Pages 212-220 | Received 23 May 2018, Accepted 24 Sep 2018, Published online: 27 Dec 2018

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Read on this site (3)

Iris Hochgraeber, Kerstin Köhler, Hannah Stöcker & Bernhard Holle. (2023) The dyadic relationship of family carers and people living with dementia – an umbrella review. Aging & Mental Health 27:10, pages 1965-1974.
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Tarja Välimäki, Anne M. Koivisto, Tuomas Selander, Toni Saari & Ilona Hallikainen. (2022) Different Trajectories of Depressive Symptoms in Alzheimer’s Disease Caregivers – 5-Year Follow-Up. Clinical Gerontologist 0:0, pages 1-10.
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Allison Gibson, Sarah D. Holmes, Noelle L. Fields & Virginia E. Richardson. (2019) Providing Care for Persons with Dementia in Rural Communities: Informal Caregivers’ Perceptions of Supports and Services. Journal of Gerontological Social Work 62:6, pages 630-648.
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Articles from other publishers (9)

Jodi Webber, Marcia Finlayson, Kathleen E. Norman & Tracy J. Trothen. (2023) Mitigating Caregiver Distress in South Western Ontario: Perspectives on Role, Community, and Care. Canadian Journal on Aging / La Revue canadienne du vieillissement, pages 1-10.
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Louis-Ferdinand Lespine, Anne-Lise Bohec, Jean-Michel Dorey, Céline Dubien Berbey, Charles Lourioux, Thierry D’amato, Marie-Odile Krebs, Isabelle Rouch & Romain Rey. (2022) Caregiving-related experiences associated with depression severity and its symptomatology among caregivers of individuals with a severe mental disorder: an online cross-sectional study. European Archives of Psychiatry and Clinical Neuroscience 273:4, pages 887-900.
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Abigail Gómez-Morales, David Coon, Rodney P Joseph & Teri Pipe. (2023) Behind the Scenes of a Technologically Enhanced Intervention for Caregivers of People With Dementia: Protocol for a Feasibility and Acceptability Study. JMIR Research Protocols 12, pages e42655.
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Helena De Sola, Inmaculada Failde, Itziar Estalella & Amaia Maquibar. (2022) Becoming a secondary actor of one's own life: A qualitative study of the experiences of informal caregivers in the care of people with chronic pain. Health Expectations 26:1, pages 409-418.
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Djin L. Tay, Eli Iacob, Maija Reblin, Kristin G. Cloyes, Miranda Jones, Megan C. Thomas Hebdon, Kathleen Mooney, Anna C. Beck & Lee Ellington. (2021) What contextual factors account for anxiety and depressed mood in hospice family caregivers?. Psycho-Oncology 31:2, pages 316-325.
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Jinpitcha Mamom & Hanvedes Daovisan. (2022) Listening to Caregivers’ Voices: The Informal Family Caregiver Burden of Caring for Chronically Ill Bedridden Elderly Patients. International Journal of Environmental Research and Public Health 19:1, pages 567.
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Aslı Gözde AKIŞ. (2021) Yaşlı Bakıcıların Bakım KariyeriCaregiving Career of Older Carers. Yaşlı Sorunları Araştırma Dergisi 14:1, pages 8-18.
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Emily West, Pushpa Nair, Yolanda Barrado-Martin, Kate R Walters, Nuriye Kupeli, Elizabeth L Sampson & Nathan Davies. (2021) Exploration of the impact of the COVID-19 pandemic on people with dementia and carers from black and minority ethnic groups. BMJ Open 11:5, pages e050066.
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Noelle L Fields, Ling Xu, Virginia E Richardson, Rupal Parekh, Dorothea Ivey & Melanie Calhoun. (2019) Utilizing the Senior Companion Program as a platform for a culturally informed caregiver intervention: Results from a mixed methods pilot study. Dementia 20:1, pages 161-187.
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