| scholarly article | Q13442814 |
| P2093 | author name string | Carol J Whitlatch | |
| Katherine S Judge | |||
| Heather L Menne | |||
| P2860 | cites work | Caregiving as a dyadic process: perspectives from caregiver and receiver | Q78027046 |
| Dyadic relationship scale: a measure of the impact of the provision and receipt of family care | Q80487029 | ||
| Disparities among older adults in measures of cognitive function by race or ethnicity | Q81137765 | ||
| A Randomized, Controlled Trial of a Home Environmental Intervention: Effect on Efficacy and Upset in Caregivers and on Daily Function of Persons With Dementia | Q22242894 | ||
| “Mini-mental state” | Q25938989 | ||
| The CES-D Scale: A Self-Report Depression Scale for Research in the General Population | Q26778378 | ||
| Acceptability and feasibility results of a strength-based skills training program for dementia caregiving dyads | Q33840958 | ||
| The structure of coping | Q34262262 | ||
| A Rating Instrument For Anxiety Disorders | Q34701881 | ||
| Outcomes for patients with dementia from the Cleveland Alzheimer's Managed Care Demonstration | Q35613826 | ||
| The sociological study of stress | Q38689697 | ||
| Dyadic intervention for family caregivers and care receivers in early-stage dementia | Q40277902 | ||
| Measuring the values and preferences for everyday care of persons with cognitive impairment and their family caregivers | Q40416989 | ||
| Decision-making for persons with cognitive impairment and their family caregivers | Q40638892 | ||
| Validity of the Quality of Well-Being Scale for patients with Alzheimer's disease | Q41642088 | ||
| Assessment of behavioral problems in dementia: the revised memory and behavior problems checklist | Q43996586 | ||
| Investigating the ways that older people cope with dementia: a qualitative study. | Q44451181 | ||
| Conflict in Alzheimer's caregiving families: its dimensions and consequences | Q44558424 | ||
| Caregiving and the stress process: an overview of concepts and their measures | Q44798910 | ||
| Behavioral problems in dementia patients and salivary cortisol patterns in caregivers | Q46531469 | ||
| Decision-making involvement of individuals with dementia | Q46810794 | ||
| Exploring race variations in aging and personal control | Q46968261 | ||
| Discovering the person with Alzheimer's disease: cognitive, emotional and behavioural aspects | Q47346453 | ||
| Spirituality and well-being: an exploratory study of the patient perspective | Q47573590 | ||
| Development of indicator scales for the Comprehensive Assessment and Referral Evaluation (CARE) interview schedule. | Q50713542 | ||
| Illness representations in early-stage dementia: a preliminary investigation. | Q50928487 | ||
| Discovering the person with Alzheimer's disease: Cognitive, emotional and behavioural aspects. | Q51067000 | ||
| Longitudinal study of quality of life in people with advanced Alzheimer's disease. | Q51067201 | ||
| The Cleveland Alzheimer's managed care demonstration: outcomes after 12 months of implementation. | Q51950355 | ||
| Effects of behavioral interventions on disruptive behavior and affect in demented nursing home residents. | Q51954300 | ||
| The perspective of the patient with Alzheimer's disease: a neglected dimension of dementia research. | Q52037084 | ||
| Predictors of institutionalization of cognitively impaired elders: family help and the timing of placement. | Q53244426 | ||
| The moderating influence of service use on negative caregiving consequences | Q71055940 | ||
| The influence of a diagnosed mental impairment on family caregiver strain | Q72388877 | ||
| Assessing quality of life in older adults with cognitive impairment | Q74138527 | ||
| The sense of control as a moderator of social class differences in health and well-being | Q74383545 | ||
| The emergence of the person in dementia research | Q74795768 | ||
| P433 | issue | 3 | |
| P921 | main subject | dementia | Q83030 |
| P304 | page(s) | 294-302 | |
| P577 | publication date | 2009-12-18 | |
| P1433 | published in | Gerontologist | Q15757423 |
| P1476 | title | Stress process model for individuals with dementia | |
| P478 | volume | 50 |
| Q50036006 | 'Because my brain isn't as active as it should be, my eyes don't always see': a qualitative exploration of the stress process for those living with posterior cortical atrophy |
| Q37690247 | A controlled trial of Partners in Dementia Care: veteran outcomes after six and twelve months. |
| Q26859831 | A practical algorithm for managing Alzheimer's disease: what, when, and why? |
| Q38171436 | Attachment in people with dementia and their caregivers: a systematic review |
| Q39123477 | Caregiver outcomes of partners in dementia care: effect of a care coordination program for veterans with dementia and their family members and friends |
| Q39970663 | Engagement of Veterans With Dementia in Partners in Dementia Care |
| Q37974384 | Forget me not: dementia in prison |
| Q28081165 | Hair Cortisol Analysis: A Promising Biomarker of HPA Activation in Older Adults |
| Q55037015 | Impact of the care coordination program "Partners in Dementia Care" on veterans' hospital admissions and emergency department visits. |
| Q44699962 | Improved Strain and Psychosocial Outcomes for Caregivers of Individuals with Dementia: Findings from Project ANSWERS. |
| Q45249676 | Including individuals with memory impairment in the research process: the importance of scales and response categories used in surveys |
| Q38995698 | Incongruent perceptions of the care values of hospitalized persons with dementia: a pilot study of patient-family caregiver dyads |
| Q48273621 | Intergenerational Ambivalence and Dyadic Strain: Understanding Stress in Family Care Partners of Older Adults |
| Q38853273 | Involvement of Hospitalized Persons With Dementia in Everyday Decisions: A Dyadic Study |
| Q50255016 | Making sense of self in Alzheimer's disease: reflective function and memory |
| Q57300324 | Mediating Effect of Mutuality on Health-Related Quality of Life in Patients with Parkinson's Disease |
| Q92358936 | Perspectives on the Delirium Experience and Its Burden: Common Themes Among Older Patients, Their Family Caregivers, and Nurses |
| Q38413551 | Predictors of Discrepancy Between Care Recipients With Mild-to-Moderate Dementia and Their Caregivers on Perceptions of the Care Recipients' Quality of Life |
| Q37167281 | Predictors of self-reported psychosocial outcomes in individuals with dementia |
| Q35141299 | Recruiting and retaining family caregivers to a randomized controlled trial on mindfulness-based stress reduction |
| Q38733678 | Stress as experienced by people with dementia: An interpretative phenomenological analysis |
| Q34473388 | Stressors and common mental disorder in informal carers--an analysis of the English Adult Psychiatric Morbidity Survey 2007 |
| Q92048955 | Supporting caregivers of veterans with Alzheimer's disease and traumatic brain injury: study protocol for a randomized controlled trial |
| Q92727273 | The associations between behavioral-psychological symptoms of dementia (BPSD) and coping strategy, burden of care and personality style among low-income caregivers of patients with dementia |
| Q91359232 | Well-being in dementia: a cross-sectional dyadic study of the impact of multiple dimensions of strain on persons living with dementia and their family care partners |
| Q36614917 | Who benefits from a psychosocial counselling versus educational intervention to improve psychological quality of life in prostate cancer survivors? |
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