NotesFAQContact Us
Collection
Advanced
Search Tips
Education Level
Audience
Counselors1
Laws, Policies, & Programs
What Works Clearinghouse Rating
Showing 1 to 15 of 17 results Save | Export
Peer reviewed Peer reviewed
Direct linkDirect link
Lauren T. Ptomey; Kelli Barton; Emma Swinford; Amy Bodde; Amanda George; Anna M. Gorczyca; C. Michelle Niedens; Susan C. Sprague; Amy Yeager; Brian Helsel; Linda Teri; Eric D. Vidoni; Jaime Perales-Puchalt – Journal of Applied Research in Intellectual Disabilities, 2024
Background: The Reducing Disability in Alzheimer's Disease in Kansas City (RDAD-KC) intervention has been shown to improve the health of individuals with dementia and caregiver dyads. This manuscript reports the results of implementing the RDAD among individuals with intellectual disabilities and caregiver dyads. Methods: Nine community agencies…
Descriptors: Alzheimers Disease, Intervention, Health Promotion, Caregivers
Peer reviewed Peer reviewed
Direct linkDirect link
Savundranayagam, Marie Y.; Orange, J. B. – International Journal of Language & Communication Disorders, 2014
Background: Communication problems stemming from Alzheimer's disease (AD) often result in misunderstandings that can be linked with problem behaviours and increased caregiver stress. Moreover, these communication breakdowns also can result either from caregivers' use of ineffective communication strategies, which paradoxically are…
Descriptors: Alzheimers Disease, Caregivers, Communication Strategies, Video Technology
Peer reviewed Peer reviewed
Direct linkDirect link
Klein, Claire M.; Silverman, Michael J. – Journal of Creativity in Mental Health, 2012
This pilot intervention compared the effects of songwriting and discussion as methods for teaching self-care to caregivers of those with dementia. The investigator led a psychoeducational discussion and a songwriting intervention with a group of caregivers, focusing on self-care. Participants answered two open-ended questions that were analyzed by…
Descriptors: Intervention, Dementia, Caregivers, Group Unity
Peer reviewed Peer reviewed
Direct linkDirect link
Carling-Jenkins, Rachel; Torr, Jennifer; Iacono, Teresa; Bigby, Christine – Journal of Intellectual & Developmental Disability, 2012
Background: Research addressing the experiences of families of adults with Down syndrome and Alzheimer's disease in seeking diagnosis and gaining support is limited. The aim of this study was to gain a greater understanding of these processes by exploring the experiences of families and carers in supporting people with Down syndrome and…
Descriptors: Alzheimers Disease, Down Syndrome, Aging (Individuals), Older Adults
Cumming, John McClure – ProQuest LLC, 2011
Caregiver burden and distress have been associated with informal caregivers. Research findings on the specific aspects of the caregiving role that influence burden are mixed. Factors such as amount of time per day giving care and specific characteristics about the disease progression have been linked to caregiver burden and distress. Other…
Descriptors: Personality Traits, Alzheimers Disease, Cancer, Caregivers
Peer reviewed Peer reviewed
Direct linkDirect link
Hilgeman, Michelle M.; Durkin, Daniel W.; Sun, Fei; DeCoster, Jamie; Allen, Rebecca S.; Gallagher-Thompson, Dolores; Burgio, Louis D. – Gerontologist, 2009
Purpose: The primary aim of this study was to test the stress process model (SPM; Pearlin, Mullan, Semple, & Skaff, 1990) in a racially diverse sample of Alzheimer's caregivers (CGs) using structural equation modeling (SEM) and regression techniques. A secondary aim was to examine race or ethnicity as a moderator of the relation between latent…
Descriptors: Ethnicity, Structural Equation Models, Academic Achievement, Caregivers
Peer reviewed Peer reviewed
Direct linkDirect link
Hayslip, Bert, Jr.; Han, GiBaeg; Anderson, Cristina L. – Educational Gerontology, 2008
This study examined similarities and differences between active caregivers (adult children and spouses whose family member had Alzheimer's disease) and not-as-yet caregiving adults (adult children and spouses whose family members are older, but do not as yet suffer from Alzheimer's disease). The objective was to determine what factors predict…
Descriptors: Spouses, Alzheimers Disease, Caregivers, Social Networks
Granello, Paul F.; Fleming, Matthew S. – ADULTSPAN Journal, 2008
Alzheimer's disease is a progressive condition that results in brain wasting and eventual death. With its increasing diagnosis rate, counselors will likely acquire clients with Alzheimer's disease or their caregivers. Important background information and several practical counseling methods are provided that may assist counselors working with this…
Descriptors: Alzheimers Disease, Caregivers, Counseling Techniques, Etiology
Peer reviewed Peer reviewed
Direct linkDirect link
Sanders, Sara; Ott, Carol H.; Kelber, Sheryl T.; Noonan, Patricia – Death Studies, 2008
An abundance of literature on caregivers of individuals with dementia has been written since the mid-1980s. However, most of this literature focused on the experience of stress, burden, and depression in caregivers, thus excluding the grief experience that also accompanies the caregiving experience. The purpose of this multimethod study is to…
Descriptors: Grief, Freedom, Alzheimers Disease, Dementia
Peer reviewed Peer reviewed
Direct linkDirect link
Whitlatch, Carol – Journal of Social Work Education, 2008
It is estimated that 13 million to 15 million adults in the United States have chronic conditions that impair cognitive function, such as Alzheimer's disease, stroke, Parkinson's disease, and traumatic brain injury. The growing number of people with chronic conditions that include cognitive impairment and the family members who assist them face…
Descriptors: Identification, Intervention, Chronic Illness, Interpersonal Relationship
Peer reviewed Peer reviewed
Morano, Carmen Louis – Social Work Research, 2003
This study focused on one question: Do caregiver responses--emotion-focused coping, problem-focused coping, appraisal of burden, and appraisal of satisfaction--mediate or moderate the effects of caregiving stress on psychological well-being? Findings indicate that development of interventions that focus on how caregivers appraise their situation,…
Descriptors: Alzheimers Disease, Caregivers, Coping, Stress Variables
Peer reviewed Peer reviewed
Novak, Mark; Guest, Carol – Gerontologist, 1989
Developed 24-item, 5-subscale Caregiver Burden Inventory (CBI) as useful diagnostic tool for professional caregivers. Administered CBI to 107 caregivers of cognitively impaired older people. Individual cases illustrated that caregivers with same total burden scores can have markedly different patterns of burden and different social and…
Descriptors: Alzheimers Disease, Caregivers, Family Role, Social Support Groups
Peer reviewed Peer reviewed
Direct linkDirect link
Aneshensel, Carol S.; Botticello, Amanda L.; Yamamoto-Mitani, Noriko – Journal of Health and Social Behavior, 2004
This study describes depressive symptoms among caregivers following bereavement and connects these trajectories to earlier features of caregiving using life course and stress process theory. Data are from a six-wave longitudinal survey (five years) of spouses and adult children caring for someone with Alzheimer's Disease. The analytic subsample (N…
Descriptors: Caring, Grief, Alzheimers Disease, Caregivers
Peer reviewed Peer reviewed
Lieberman, Morton A.; Fisher, Lawrence – Gerontologist, 1995
Explored the impact of dementia on family members' physical and mental health while caring for an ill parent/spouse. Severity of illness was significantly associated with health and well-being for spouses, offspring, and in-laws, regardless of the amount of caregiving. Demonstrates the potential cascading effect of severe illness. (RJM)
Descriptors: Alzheimers Disease, Caregivers, Chronic Illness, Comparative Analysis
Peer reviewed Peer reviewed
Cox, Carole – Social Work, 1995
Using a conceptual stress development model that treats informal supports and competency as potential mediators, examined outcomes of caregiving in samples of black and white caregivers. A perceived lack of informal supports and a sense of incompetency exacerbated stress among black caregivers but had no effects among the white caregivers. (RJM)
Descriptors: Alzheimers Disease, Blacks, Caregiver Attitudes, Caregiver Role
Previous Page | Next Page ยป
Pages: 1  |  2