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Subject Areas on Research
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"He Needed Just About Everything": Caring for Aging Adults Postincarceration.
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"I know that my role is going to change": a mixed-methods study of the relationship between amyloid-β PET scan results and caregiver burden.
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"I've been always strong to conquer any suffering:" challenges and resilience of Chinese American dementia caregivers in a life course perspective.
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"Just tell me in a simple way": A qualitative study on opportunities to improve the transition from acute hospital care to home from the perspectives of patients with traumatic brain injury, families, and providers.
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"Now at least we have something to call it": Patient and care partner experiences receiving an amyloid PET scan.
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'The face of the programme': How local clinicians shape decisions about eligibility for a national caregiver support programme in the USA.
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A Blue Ocean Strategy for Palliative Care: Focus on Family Caregivers.
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A Couple-Based Communication Intervention for Hematopoietic Cell Transplantation Survivors and Their Caregiving Partners: Feasibility, Acceptability, and Change in Process Measures.
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A Developmental Analysis of Caregiving Modalities Across Infancy in 38 Low- and Middle-Income Countries.
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A Methodological Approach for Documenting Multi-Component Interventions Targeting Family Caregivers.
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A Mixed-Methods Study of the Impact of Mild Cognitive Impairment Diagnosis on Patient and Care Partner Perception of Health Risks.
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A Multicenter Trial of a Shared Decision Support Intervention for Patients and Their Caregivers Offered Destination Therapy for Advanced Heart Failure: DECIDE-LVAD: Rationale, Design, and Pilot Data.
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A New Era in Cardiac Rehabilitation Delivery: Research Gaps, Questions, Strategies, and Priorities.
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A North Carolina service for those with questions about Alzheimer disease, other memory disorders, and family care.
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A Person-Centered Approach to Poststroke Care: The COMprehensive Post-Acute Stroke Services Model.
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A Prospective Longitudinal Study of Caregivers of Community Dwelling Persons with Severe Dementia (PISCES): Study Protocol.
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A comparative qualitative analysis of stories of spousal caregivers of people with dementia: negative, ambivalent, and positive experiences.
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A comparison of the wellbeing of orphans and abandoned children ages 6-12 in institutional and community-based care settings in 5 less wealthy nations.
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A conceptual framework of outcomes for caregivers of assistive technology users.
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A modified DBT skills training program for oppositional defiant adolescents: promising preliminary findings.
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A path model of chronic stress, the metabolic syndrome, and coronary heart disease.
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A pilot study on the influence of an individualized and experiential training on cancer caregiver's self-efficacy in home care and symptom management.
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A prospective cohort study of decision-making role preferences of patients with advanced cancer and their family caregivers.
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A prospective study of psychological distress among patients with advanced cancer and their caregivers.
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A randomized controlled trial on rehabilitation through caregiver-delivered nurse-organized service programs for disabled stroke patients in rural china (the RECOVER trial): design and rationale.
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A scoping review of person and family engagement in the context of multiple chronic conditions.
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A service user co-facilitated intervention to reduce mental illness stigma among primary healthcare workers: Utilizing perspectives of family members and caregivers.
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A single-site pilot feasibility randomized trial of a supportive care mobile application intervention for patients with advanced cancer and caregivers.
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ALS clinical research learning institutes (ALS-CRLI): empowering people with ALS to be research ambassadors.
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Academic-Practice Partnership for Caregiver Training and Support: The Duke Elder Family/Caregiver Training (DEFT) Center.
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Acceptability of a Dyadic Psychoeducational Intervention for Patients and Caregivers.
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Acceptability of a group intervention for initiates of antiretroviral therapy in Tanzania.
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Adaptation and Implementation of a Family Caregiver Skills Training Program: From Single Site RCT to Multisite Pragmatic Intervention.
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Adapters, strugglers, and case managers: a typology of spouse caregivers.
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Adjustment of caregivers of pediatric patients with brain tumors: a cross-sectional analysis.
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Adolescents and parental caregivers as lay health advisers in a community-based risk reduction intervention for youth: baseline data from Teach One, Reach One.
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Adolescents' and caregivers' perceptions of caregiver-provided testing and HIV self-testing using oral mucosal transudate tests in Zimbabwe: a short report.
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Advance Directive Preferences Among Terminally Ill Older Patients and Its Facilitators and Barriers in China: A Scoping Review.
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Advance directives among cognitively impaired persons who had an amyloid PET scan and their care partners: a mixed-methods study.
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Advances in mediation analysis can facilitate nursing research.
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Advancing Palliative Care Integration in Hematology: Building Upon Existing Evidence.
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Adverse childhood experiences, psychosocial well-being and cognitive development among orphans and abandoned children in five low income countries.
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Agreement Between Child Self-report and Caregiver-Proxy Report for Symptoms and Functioning of Children Undergoing Cancer Treatment.
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Alcohol, drug, and mental health specialty treatment services and race/ethnicity: a national study of children and families involved with child welfare.
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Alzheimer's disease and the family caregiver: the cost and who pays?
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Ambivalence over emotional expression in patients with gastrointestinal cancer and their caregivers: associations with patient pain and quality of life.
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An Evaluation of Websites Offering Caregiver Education for Tracheostomy and Home Mechanical Ventilation.
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An organizing framework for informal caregiver interventions: detailing caregiving activities and caregiver and care recipient outcomes to optimize evaluation efforts.
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Anxiety and Depressive Symptoms Among Two Seriously Medically Ill Populations and Their Family Caregivers: A Comparison and Clinical Implications.
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Application of assessing care of vulnerable elders-3 quality indicators to patients with advanced dementia and poor prognosis.
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Assessing patients' and caregivers' perspectives on stability of factor VIII products for haemophilia A: a web-based study in the United States and Canada.
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Assessing the Role of the Family/Support System Perspective in Patients With Glaucoma.
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Assessing trauma and related distress in refugee youth and their caregivers: should we be concerned about iatrogenic effects?
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Assessment of Caregiver Inventory for Rett Syndrome.
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Assessment of health literacy and numeracy among Spanish-Speaking parents of young children: validation of the Spanish Parental Health Literacy Activities Test (PHLAT Spanish).
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Assessment of young children's social-emotional development and psychopathology: recent advances and recommendations for practice.
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Association between primary caregiver type and mortality among Chinese older adults with disability: a prospective cohort study.
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Association of anxiety and depression with pulmonary-specific symptoms in chronic obstructive pulmonary disease.
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Association of dementia comorbidities with caregivers' physical, psychological, social, and financial burden.
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Association of formal and informal care with health-related quality of life and depressive symptoms: findings from the Caring for Adults Recovering from the Effects of Stroke study.
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Associations Between Alzheimer's Disease and Related Dementias and Depressive Symptoms of Partner Caregivers.
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Associations among perceptions of social support, negative affect, and quality of sleep in caregivers and noncaregivers.
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Associations between child disabilities and caregiver discipline and violence in low- and middle-income countries.
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Associations of home food availability, dietary intake, screen time and physical activity with BMI in young American-Indian children.
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Attachment and pain: recent findings and future directions.
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Barriers to care in juvenile localized and systemic scleroderma: an exploratory survey study of caregivers' perspectives.
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Barriers to medication adherence in a rural-urban dual economy: a multi-stakeholder qualitative study.
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Beliefs about promoting cognitive health among Filipino Americans who care for persons with dementia.
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Benefit Finding in Maternal Caregivers of Pediatric Cancer Survivors: A Mixed Methods Approach.
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Biopsychosocial experiences and coping strategies of elderly ESRD patients: a qualitative study to inform the development of more holistic and person-centred health services in Singapore.
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Body image perceptions and dieting among African-American pre-adolescent girls and parents/caregivers.
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Brief report: psychosocial functioning of fathers as primary caregivers of pediatric oncology patients.
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Bringing Invisible Partners in Care out of the Shadows: Employment Effects of Informal Care Provision in Europe and Implications for the United States.
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Building resilience: a mental health intervention for Tanzanian youth living with HIV.
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Burden and mental health among caregivers of veterans with traumatic brain injury/polytrauma.
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Burden and well-being among a diverse sample of cancer, congestive heart failure, and chronic obstructive pulmonary disease caregivers.
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Burden of informal care in stroke survivors and its determinants: a prospective observational study in an Asian setting.
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Busy/dying.
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Can caregivers report their care recipients' post-stroke hospitalizations and outpatient visits accurately? Findings of an Asian prospective stroke cohort.
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Canadian study of health and aging: study methods and prevalence of dementia.
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Care Coordination Processes in Transitional Care for Patients With Heart Failure: An Integrative Review Through a Social Network Lens.
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Care partner-assisted intervention to improve oral health for older adults with cognitive impairment: A feasibility study.
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Care transitions from the hospital to home for patients with mobility impairments: patient and family caregiver experiences.
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Caregiver Burden as a Mediator Between Emotional Distress and Concentration Problems in Patients With Cancer.
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Caregiver Characteristics Associated With Cognitive Complaints in Women With Breast Cancer.
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Caregiver Health-Related Quality of Life, Burden, and Patient Outcomes in Ambulatory Advanced Heart Failure: A Report From REVIVAL.
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Caregiver Inclusivity and Empowerment During Family-Centered Rounds.
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Caregiver Preferences for the Treatment of Males with Fragile X Syndrome.
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Caregiver Quality of Life Is Related to Severity of Otitis Media in Children.
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Caregiver burden and its associated factors among family caregivers of persons with dementia in Shanghai, China: a cross-sectional study.
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Caregiver burden and psychological distress in partners of veterans with chronic posttraumatic stress disorder.
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Caregiver burden and well-being: an elusive distinction.
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Caregiver burden by treatment and clinical characteristics of patients with glioblastoma.
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Caregiver burden in partners of Vietnam War veterans with posttraumatic stress disorder.
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Caregiver experience during advanced chronic illness and last year of life.
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Caregiver intervention research: an opportunity for collaboration between caregiving investigators and African-american faith communities.
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Caregiver psychological distress as a barrier to influenza vaccination among community-dwelling elderly with dementia.
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Caregiver ratings of personality change in Alzheimer's disease patients: a replication.
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Caregiver role in HIV medication adherence among HIV-infected orphans in Tanzania.
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Caregiver self-efficacy to talk about sex predicts conversations about HIV transmission risk with perinatally infected young people in Zimbabwe.
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Caregiver strain and youth suicide attempt: Are they related?
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Caregiver-Delivered Stroke Rehabilitation in Rural China.
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Caregiver-Reported Roles in Treatment Decision Making in Advanced Cancer and Associated Caregiving Burden and Psychological Distress: A Longitudinal Study.
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Caregiver-Reported Sleep Disturbances Are Associated With Behavioral and Psychological Symptoms in an Asian Elderly Cohort With Cognitive Impairment-No Dementia.
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Caregiver-assisted coping skills training for lung cancer: results of a randomized clinical trial.
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Caregiver-assisted coping skills training for patients with COPD: background, design, and methodological issues for the INSPIRE-II study.
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Caregiver-guided pain coping skills training for patients with advanced cancer: Background, design, and challenges for the CaringPals study.
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Caregiver-guided pain coping skills training for patients with advanced cancer: Results from a randomized clinical trial.
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Caregiver-recipient closeness and symptom progression in Alzheimer disease. The Cache County Dementia Progression Study.
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Caregivers as money managers for adults with severe mental illness: how treatment providers can help.
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Caregivers in China: knowledge of mild cognitive impairment.
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Caregivers of Black and Latino/a/x Students and School Personnel Perspectives on School-Based SARS-CoV-2 Testing: Implications for Testing and Test-to-Stay Programs in K-12 Schools.
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Caregivers of Patients Considering a Destination Therapy Left Ventricular Assist Device and a Shared Decision-Making Intervention: The DECIDE-LVAD Trial.
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Caregivers' perception of the role of the socio-environment on their extremely preterm child's well-being.
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Caregivers' reasons for nursing home placement: clues for improving discussions with families prior to the transition.
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Caregivers' role in managing hereditary angioedema and perceptions of treatment-related burden.
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Caregiving behavior is associated with decreased mortality risk.
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Caregiving for persons with mental illness: the impact of outpatient commitment on caregiving strain.
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Caregiving intensity and retirement status in Canada.
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Caregiving networks of elderly persons: variation by marital status.
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Caregiving, residence, race, and depressive symptoms.
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Caregiving-related needs of family caregivers of older Singaporeans.
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Caring for Caregivers During COVID-19.
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Caring for Caregivers-A New Integrative Care Path for Advanced Lung Cancer Patients and Their Caregivers.
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Caring for Children With Medical Complexity With the Emergency Information Form.
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Caring for frail older adults: a theoretical and methodological agenda.
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Caring for individuals with dementia and cognitive impairment, not dementia: findings from the aging, demographics, and memory study.
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Caring for mom and neglecting yourself? The health effects of caring for an elderly parent.
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Challenges of optimizing glycaemic control in children with Type 1 diabetes: a qualitative study of parents' experiences and views.
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Change in Caregivers' Attitudes and Use of Corporal Punishment Following a Legal Ban: A Multi-Country Longitudinal Comparison.
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Child and adult victimization: sequelae for female caregivers of high-risk children.
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Child-Adult Relationship Enhancement (CARE): An evidence-informed program for children with a history of trauma and other behavioral challenges.
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Childhood traumatic grief: a multi-site empirical examination of the construct and its correlates.
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Children of Alzheimer patients: an overview.
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Children with Chronic Lung Disease: Facilitating Smoking Cessation for their Caregivers.
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Chronic family stress moderates the association between a TOMM40 variant and triglyceride levels in two independent Caucasian samples.
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Chronic pain-associated behaviors in the nursing home: resident versus caregiver perceptions.
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Clinical Validation of the Autism Behavior Inventory: Caregiver-Rated Assessment of Core and Associated Symptoms of Autism Spectrum Disorder.
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Clinical assessment of medication adherence among HIV-infected children: examination of the Treatment Interview Protocol (TIP).
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Clinical trial testing in-home multidisciplinary care management for older adults with cognitive vulnerability: Rationale and study design.
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Cognitive performance and informant reports in the diagnosis of cognitive impairment and dementia in African Americans and whites.
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Cohort profile for the Nurture Observational Study examining associations of multiple caregivers on infant growth in the Southeastern USA.
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Commentary: Sir Arthur Mitchell--pioneer of psychiatric epidemiology and of community care.
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Community-Based Long-Term Care Services: If We Build It, Will They Come?
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Comparison of preferences for end-of-life care among patients with advanced cancer and their caregivers: A discrete choice experiment.
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Compassion fatigue in adult daughter caregivers of a parent with dementia.
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Complexities and Challenges of Singapore Nurses Providing Postacute Home Care in Multicultural Communities: A Grounded Theory Study.
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Components and correlates of family burden in schizophrenia.
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Comprehensive Support for Family Caregivers of Post-9/11 Veterans Increases Veteran Utilization of Long-term Services and Supports: A Propensity Score Analysis.
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Comprehensive Support for Family Caregivers: Impact on Veteran Health Care Utilization and Costs.
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Comprehensive support of family caregivers: Are there health system cost offsets?
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Conducting caregiver focus groups on autism in the context of an international research collaboration: Logistical and methodological lessons learned in South Africa.
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Confirmatory factor analysis of the Infant Feeding Styles Questionnaire in Latino families.
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Connect-Home: Transitional Care of Skilled Nursing Facility Patients and their Caregivers.
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Connecting Caregivers to Support: Lessons Learned From the VA Caregiver Support Program.
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Consensus statement on depression, anxiety, and oncology.
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Consumer, provider, and informal caregiver opinions on psychiatric advance directives.
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Contextualization of psychological treatments for government health systems in low-resource settings: group interpersonal psychotherapy for caregivers of children with nodding syndrome in Uganda.
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Contribution of neuropsychiatric symptoms in Parkinson's disease to different domains of caregiver burden.
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Coping Skills Practice and Symptom Change: A Secondary Analysis of a Pilot Telephone Symptom Management Intervention for Lung Cancer Patients and Their Family Caregivers.
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Coping in caregivers of patients with hematologic malignancies undergoing hematopoietic stem cell transplantation.
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Coronary catherization patient and wife's perceptions of social support: effects due to characteristics of recipient, provider, and their interaction.
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Coronary heart disease moderates the relationship of chronic stress with the metabolic syndrome.
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Correlates of care relationship mutuality among carers of people with Alzheimer's and Parkinson's disease.
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Correlates of poor health among orphans and abandoned children in less wealthy countries: the importance of caregiver health.
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Cross Country Comparison of Expert Assessments of the Quality of Death and Dying 2021.
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Culturally and developmentally adapting group interpersonal therapy for adolescents with depression in rural Nepal.
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Deciding to institutionalize: why do family members cease caregiving at home?
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Decision Aid Interventions for Family Caregivers of Persons With Advanced Dementia in Decision-Making About Feeding Options: A Scoping Review.
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Defining High-Quality Palliative Care in Oncology Practice: An American Society of Clinical Oncology/American Academy of Hospice and Palliative Medicine Guidance Statement.
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Defining the Clinical, Emotional, Social, and Financial Burden of Congenital Athymia.
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Dementia and cancer: a comparison of spouse caregivers.
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Dementia assessment and management.
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Dementia caregiver interventions in Chinese people: A systematic review.
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Dementia in relation to family caregiver involvement and burden in long-term care.
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Dental care utilization among caregivers who care for older adults.
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Depression in primary caregivers of patients listed for liver or kidney transplantation.
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Depressive Symptoms and Caregiving Intensity Before and After Onset of Dementia in Partners: A Retrospective, Observational Study.
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Depressive symptoms among informal caregivers of older adults: insights from the Singapore Survey on Informal Caregiving.
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Design, methods, and baseline characteristics of the Brain Injury Education, Training, and Therapy to Enhance Recovery (BETTER) feasibility study: a transitional care intervention for younger adult patients with traumatic brain injury and caregivers.
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Designing a Primary Care-Based Deprescribing Intervention for Patients with Dementia and Multiple Chronic Conditions: a Qualitative Study.
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Developing a person-centered, population based measure of "home time": Perspectives of older patients and unpaid caregivers.
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Developing a toolkit to improve resident and family engagement in the safety of assisted living: Engage-A stakeholder-engaged research protocol.
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Developing lay summaries and thank you notes in paediatric pragmatic clinical trials.
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Development and Initial Validation of the Caregiver Perceptions About Communication With Clinical Team Members (CAPACITY) Measure.
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Development and preliminary evaluation of a telephone-based coping skills training intervention for survivors of acute lung injury and their informal caregivers.
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Development and preliminary evaluation of a telephone-based mindfulness training intervention for survivors of critical illness.
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Development and preliminary evaluation of the caregiver assistive technology outcome measure.
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Development and validation of the Psychological Adaptation Scale (PAS): use in six studies of adaptation to a health condition or risk.
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Development and validation of the parent experience of child illness.
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Diagnostic preferences include discussion of etiology for adults with cerebral palsy and their caregivers.
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Differential attrition in a caregiver skill training trial.
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Differential levels of stress in caregivers of brain tumor patients--observations from a pilot study.
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Direct social support for young high risk children: relations with behavioral and emotional outcomes across time.
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Directed content analysis of Veterans Affairs policy documents: A strategy to guide implementation of a dementia home safety toolkit for Veterans to promote ageing in place.
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Discordance between dementia caregivers' goal of care and preference for life-extending treatments.
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Do nurse-led skill training interventions affect informal caregivers' out-of-pocket expenditures?
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Does Caregiving Strain Increase as Patients With and Without Dementia Approach the End of Life?
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Does a helping hand mean a heavy heart? Helping behavior and well-being among spouse caregivers.
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Does support from foreign domestic workers decrease the negative impact of informal caregiving? Results from Singapore survey on informal caregiving.
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Domestic helpers as frontline workers in China's home-based elder care: A systematic review.
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Donepezil for treatment of cognitive dysfunction in children with Down syndrome aged 10-17.
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Doris Duke Charitable Foundation Fund to Retain Clinical Scientists: innovating support for early-career family caregivers.
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Drivers of Long-Term Care Considerations by Persons With Cognitive Impairment.
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Dyadic approach to post-stroke hospitalizations: role of caregiver and patient characteristics.
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Dyadic approach to supervised community rehabilitation participation in an Asian setting post-stroke: exploring the role of caregiver and patient characteristics in a prospective cohort study.
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Dyadic psychosocial interventions for patients with cancer and their caregivers: an update.
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EMPOWER: an intervention to address barriers to pain management in hospice.
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Early Peanut Protein Introduction in Clinical Practice.
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Early Survivorship After Liver Transplantation: A Qualitative Study Identifying Challenges in Recovery From the Patient and Caregiver Perspective.
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Early caregiving stress exposure moderates the relation between respiratory sinus arrhythmia reactivity at 1 month and biobehavioral outcomes at age 3.
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Early integration of palliative care into the care of patients with cancer.
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Economic Spillover Effects of Intensive Unpaid Caregiving.
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Economic burden for informal caregivers of lung and colorectal cancer patients.
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Education on the consequences of traumatic brain injury for children and adolescents with TBI and families/caregivers: a systematic scoping review.
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Effect of Inpatient Palliative Care on Quality of Life 2 Weeks After Hematopoietic Stem Cell Transplantation: A Randomized Clinical Trial.
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Effect of Palliative Care-Led Meetings for Families of Patients With Chronic Critical Illness: A Randomized Clinical Trial.
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Effect of a tailored assistive technology intervention on older adults and their family caregiver: a pragmatic study protocol.
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Effect of predicted low suspend pump treatment on improving glycaemic control and quality of sleep in children with type 1 diabetes and their caregivers: the QUEST randomized crossover study.
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Effect of race on cultural justifications for caregiving.
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Effects of 5HTTLPR on cardiovascular response to an emotional stressor.
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Effects of a Telephone- and Web-based Coping Skills Training Program Compared with an Education Program for Survivors of Critical Illness and Their Family Members. A Randomized Clinical Trial.
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Effects of a caregiver-inclusive assistive technology intervention: a randomized controlled trial.
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Effects of a hybrid education program for Korean mothers of children with atopic dermatitis.
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Effects of an Individualized Caregiver Training Intervention on Self-Efficacy of Cancer Caregivers.
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Effects of enhanced caregiver training program on cancer caregiver's self-efficacy, preparedness, and psychological well-being.
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Effects of environmental stress and gender on associations among symptoms of depression and the serotonin transporter gene linked polymorphic region (5-HTTLPR).
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Effects of spouse-assisted coping skills training and exercise training in patients with osteoarthritic knee pain: a randomized controlled study.
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Effects of the child-perpetrator relationship on mental health outcomes of child abuse: it's (not) all relative.
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Efficacy and cost-effectiveness of an outcall program to reduce carer burden and depression among carers of cancer patients [PROTECT]: rationale and design of a randomized controlled trial.
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Efficacy of a telephone outcall program to reduce caregiver burden among caregivers of cancer patients [PROTECT]: a randomised controlled trial.
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Emergency Department Communication in Persons Living With Dementia and Care Partners: A Scoping Review.
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Emotional distress and quality of life in caregivers of patients awaiting lung transplant.
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Engaging ALS patients and caregivers (the ALS research ambassadors) to help design the REFINE-ALS biomarker study.
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Engaging communities in evidence-based interventions for dementia caregivers.
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Engaging patients and families to create a feasible clinical trial integrating palliative and heart failure care: results of the ENABLE CHF-PC pilot clinical trial.
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Enhancement of Aging in Place: An Evolving Understanding of Person-Centered Dementia Care in Home Settings.
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Enhancing & Mobilizing the POtential for Wellness & Emotional Resilience (EMPOWER) among Surrogate Decision-Makers of ICU Patients: study protocol for a randomized controlled trial.
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Enuresis in children and adolescents with sickle cell anaemia is more frequent and substantially different from the general population.
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Epidemiology of apathy in older adults: the Cache County Study.
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Equal division of estates and the exchange motive.
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Essential Long-Term Care Workers Commonly Hold Second Jobs and Double- or Triple-Duty Caregiving Roles.
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Establishing the first community-centered Spina Bifida research agenda.
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Evaluating the Feasibility and Acceptability of a Telehealth Program in a Rural Palliative Care Population: TapCloud for Palliative Care.
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Evaluation of a discharge education protocol for pediatric patients with gastrostomy tubes.
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Examining dual method contraceptive use among midwestern parenting Latinx teens: Perspectives from adolescent parents, caretakers, and nurses.
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Examining the Influence of Social Interactions and Community Resources on Caregivers' Burden in Stroke Settings: A Prospective Cohort Study.
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Examining the interrelatedness of patient and spousal stress in heart failure: conceptual model and pilot data.
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Expectations and outcomes of gastric feeding tubes.
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Expectations and outcomes of prolonged mechanical ventilation.
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Expenditures in caring for patients with dementia who live at home.
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Experiences and concerns of family caregivers providing support to people with dementia: A cross-cultural perspective
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Experiences of Family Caregivers After an Acute Neurological Event.
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Experiences of Family Caregivers of People with Dementia during the COVID-19 Pandemic.
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Experiences with health care practitioners among advanced cancer patients and their family caregivers: A longitudinal dyadic study.
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Expert estimates of caregiver hours for older Singaporeans with dementia.
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Exploring Communication Ability in Individuals With Angelman Syndrome: Findings From Qualitative Interviews With Caregivers.
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Exploring Culturally Responsive Religious and Spirituality Health Care Communications among African Americans with Advanced Heart Failure, Their Family Caregivers, and Clinicians.
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Exploring the Feasibility and Acceptability of Providing Caregivers Who Formula-feed with Smaller Infant Bottles in a Primary Care Clinic.
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Exploring the challenges and needs of home caregivers of hemodialysis patients in the Philippines: A mixed methods study.
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Exploring the impact of paediatric localized scleroderma on health-related quality of life: focus groups with youth and caregivers.
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Exploring the meaning of childhood disability: perceptions of disability among mothers of children with disabilities (CWD) in Kuwait.
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Eye-tracking measures of social versus nonsocial attention are related to level of social engagement during naturalistic caregiver-child interactions in autistic children.
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FAMILY CAREGIVER'S PERCEPTION OF DEMENTIA AND CAREGIVING IN CHINESE CULTURE
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Facilitating research participation and improving quality of life for African American prostate cancer survivors and their intimate partners. A pilot study of telephone-based coping skills training.
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Factors That Impact Family Perception of Goal-Concordant Care at the End of Life.
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Factors associated with caregiver burden among caregivers of children with cerebral palsy in Sri Lanka.
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Factors considered important at the end of life by patients, family, physicians, and other care providers.
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Family Caregiver Perspectives on Suffering of Persons With Severe Dementia: A Qualitative Study.
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Family Caregiver Skills Training to Improve Experiences of Care: a Randomized Clinical Trial.
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Family Caregiver and Provider Perspectives on Inclusive Care: Aligning Needs and Expectations.
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Family Caregivers of Veterans Experience Clinically Significant Levels of Distress Prepandemic and During Pandemic: Implications for Caregiver Support Services.
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Family care and Alzheimer's disease: what do we know? What can we do?
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Family caregiver satisfaction with inpatient rehabilitation care.
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Family caregivers of advanced cancer patients: self-perceived competency and meaning-making.
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Family dynamics in a multi-ethnic Asian society: comparison of elderly CKD patients and their family caregivers experience with medical decision making for managing end stage kidney disease.
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Family issues in dementia: finding a new normal.
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Family systemic psychosocial support for at-risk adolescents in Lebanon: study protocol for a multi-site randomised controlled trial.
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Family-Centered Care for Children and Families Impacted by Neonatal Seizures: Advice From Parents.
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Family-supportive supervisor behaviour positively affects work behaviour and nonwork well-being among men in long-term care.
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Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life.
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Feasibility and Acceptability of a Remotely Delivered Weighted Blanket Intervention for People Living With Dementia and Their Family Caregivers.
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Feasibility of a dyadic intervention for management of osteoarthritis: a pilot study with older patients and their spousal caregivers.
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Feasibility of an adaptive riding pilot study and acceptability to dementia care partners: "Your spirits are lifted".
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Feeding a family in a recession: food insecurity among Minnesota parents.
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Feeding dysfunction in single ventricle patients with feeding disorder.
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Financial burden for caregivers of adolescents and young adults with cancer.
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Financial hardships and psychosocial outcomes among parents of children who die of cancer.
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Financial toxicity among individuals with spina bifida and their families: A qualitative study and conceptual model.
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Finding meaning in caring for a spouse with dementia.
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Formative research methods for designing culturally appropriate, integrated child nutrition and development interventions: an overview.
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From Barriers to Assets: Rethinking factors impacting advance care planning for African Americans.
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From Stigma to Validation: A Qualitative Assessment of a Novel National Program to Improve Retention of Physician-Scientists with Caregiving Responsibilities.
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From evidence to practice: using the RE-AIM framework to adapt the REACHII caregiver intervention to the community.
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Great expectations: a position description for parents as caregivers: Part I.
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Great expectations: a position description for parents as caregivers: Part II.
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Greater risk of dementia when spouse has dementia? The Cache County study.
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HIV+ caregivers and HIV+ non-caregivers: differences in sociodemographics, immune functioning, and quality-of-life.
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HPA axis function in male caregivers: effect of the monoamine oxidase-A gene promoter (MAOA-uVNTR).
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Head and Neck Cancer Survivors: Specific Needs and Their Implications for Survivorship Care Planning.
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Health Trajectories of Women in China: The Role of Parental Caregiving.
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Health and social care of home-dwelling frail older adults in Switzerland: a mixed methods study.
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Health impacts of caregiving for older adults with functional limitations: results from the Singapore survey on informal caregiving.
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Health literacy and injury prevention behaviors among caregivers of infants.
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Health values of the seriously ill. SUPPORT investigators.
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Health, wellness, and safety concerns of persons with moderate-to-severe traumatic brain injury and their family caregivers: a qualitative content analysis.
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Healthcare retention and clinical outcomes among adolescents living with HIV after transition from pediatric to adult care: a systematic review.
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Healthcare utilization and cost trajectories post-stroke: role of caregiver and stroke factors.
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Helping Dementia Caregivers Manage Medical Problems: Benefits of an Educational Resource.
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Helping Invested Families Improve Veterans' Experiences Study (HI-FIVES): study design and methodology.
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Home automated external defibrillators in a geriatric population: a brief discussion of the evidence.
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Home tonometry for management of pediatric glaucoma.
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Hope in the era of precision oncology: a qualitative study of informal caregivers' experiences.
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Hoping for the best and preparing for the worst: a forgotten maxim in the immunotherapy era?
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Hospice education about people with AIDS as terminally ill patients: coping with a new epidemic of death.
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How Accurately Do Patients and Their Care Partners Report Results of Amyloid-β PET Scans for Alzheimer's Disease Assessment?
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How Caregivers Cope and Adapt When a Family Member Is Diagnosed With a Hematologic Malignancy: Informing Supportive Care Needs.
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How Surrogate Decision-Makers for Patients With Chronic Critical Illness Perceive and Carry Out Their Role.
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How should we implement psychiatric advance directives? Views of consumers, caregivers, mental health providers and researchers.
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Identifying Core Domains to Assess the "Quality of Death": A Scoping Review.
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Identifying critically important cardiovascular outcomes for trials in hemodialysis: an international survey with patients, caregivers and health professionals.
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Identifying trajectories of depressive symptoms for women caring for their husbands with dementia.
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Identifying treatment effects of an informal caregiver education intervention to increase days in the community and decrease caregiver distress: a machine-learning secondary analysis of subgroup effects in the HI-FIVES randomized clinical trial.
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Identifying, recruiting, and retaining seriously-ill patients and their caregivers in longitudinal research.
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If patients are the true north, patient-centeredness should guide research.
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Impact of COVID-19 on the Onset and Progression of Alzheimer's Disease and Related Dementias: A Roadmap for Future Research.
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Impact of Chronic Sleep Disturbance for People Living With T1 Diabetes.
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Impact of San Francisco's toy ordinance on restaurants and children's food purchases, 2011-2012.
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Impact of TBI on caregivers of veterans with TBI: Burden and interventions.
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Impact of Type 1 Diabetes Technology on Family Members/Significant Others of People With Diabetes.
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Impact of a Hematologic Malignancy Diagnosis and Treatment on Patients and Their Family Caregivers.
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Impact of antipsychotic medication on family burden in schizophrenia: longitudinal results of CATIE trial.
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Impact of patients' psychiatric hospitalization on caregivers: a systematic review.
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Impact of psychological stress on the associations between apolipoprotein E variants and metabolic traits: findings in an American sample of caregivers and controls.
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Impact of treatment improvement on long-term anxiety: Results from CAMS and CAMELS.
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Impact on family and parental stress of prenatal vs postnatal repair of myelomeningocele.
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Impacts of COVID-19 on caregivers of childhood cancer survivors.
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Implementing a Standardized Transition Care Plan in Skilled Nursing Facilities.
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Implementing a pediatric oncology nursing multisite trial.
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Improving the quality of cancer care in an aging population: recommendations from an IOM report.
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Improving the quality of survivorship for older adults with cancer.
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Including Family Caregivers In Seriously Ill Veterans' Care: A Mixed-Methods Study.
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Inclusion of Caregivers in Veterans' Care: A Critical Literature Review.
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Individual and program Characteristics May Drive Variability in Outcomes After Caregivers Participate in a Tailored Support Intervention.
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Individual- and family-level psychosocial correlates of HIV risk behavior among youth in rural Kenya.
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Infant and Toddler Child-Care Quality and Stability in Relation to Proximal and Distal Academic and Social Outcomes.
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Influence of Caretakers' Health Literacy on Delays to Traumatic Brain Injury Care in Uganda.
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Influence of Temperament As a Risk Indicator for Early Childhood Caries.
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Influence of mild cognitive impairment on patient and care partner decision-making for acute ischemic stroke.
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Influenza vaccination practices of physicians and caregivers of children with neurologic and neurodevelopmental conditions - United States, 2011-12 influenza season.
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Informal And Formal Home Care For Older Adults With Disabilities Increased, 2004-16.
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Informal Caregiver Disability and Access to Preventive Care in Care Recipients.
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Informal Caregiver Support Policies Change Use of Vocational Assistance Services for Individuals With Disabilities.
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Informal Caregiving: A Growing Need for Inclusion in Stroke Rehabilitation.
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Informal and formal care infrastructure and perceived need for caregiver training for frail US veterans referred to home and community-based services.
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Informal care and Medicare expenditures: testing for heterogeneous treatment effects.
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Informal care and caregiver's health.
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Informal caregiver training on home care and cancer symptom management prior to hospital discharge: a feasibility study.
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Informal caregivers' burden and stress in caring for stroke survivors with spatial neglect: an exploratory mixed-method study.
-
Intensity of grandparent caregiving and life satisfaction among rural chinese older adults: a longitudinal study using latent difference score analysis.
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Internet Use and Technology-Related Attitudes of Veterans and Informal Caregivers of Veterans.
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Intervention design in cognitively impaired populations-Lessons learned from the OPTIMIZE deprescribing pragmatic trial.
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Interventions That Support or Involve Caregivers or Families of Patients with Traumatic Injury: a Systematic Review.
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Interviews with caregivers during acute asthma hospitalisations.
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Is policy well-targeted to remedy financial strain among caregivers of severely injured U.S. service members?
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Is there no place like home? Caregivers recall reasons for and experience upon transfer from home hospice to inpatient facilities.
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Lack of Concordance in Symptomatic Adverse Event Reporting by Children, Clinicians, and Caregivers: Implications for Cancer Clinical Trials.
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Language processing deficits in sickle cell disease in young school-age children.
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Lessons learned from a Parkinson's disease caregiver intervention pilot study.
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Levels of stress and intervention preferences of caregivers of brain tumor patients.
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Leveraging institutional support for family caregivers to meet the health and vocational needs of persons with disabilities.
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Life After the Neurosurgical Ward in Sub-Saharan Africa: Neurosurgical Treatment and Outpatient Outcomes in Uganda.
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Living With Cognitive Impairment in China: Exploring Dyadic Experiences Through a Person-Centered Care Lens.
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Long-term care insurance: Does experience matter?
-
Longitudinal Assessment of Self-Harm Statements of Youth in Foster Care: Rates, Reporters, and Related Factors.
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Longitudinal trajectories of caregiving experiences among primary informal caregivers of patients with metastatic solid cancer (stage IV).
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Machine learning approach to measurement of criticism: The core dimension of expressed emotion.
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Management of patients with Parkinson disease.
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Managing Visitors During the Hospital Stay: The Experience of Family Caregivers of Patients With Traumatic Brain Injury.
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Managing challenging behaviors at home.
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Mandated Caregiver Training in the Veterans Health Administration: Caregiver Inquiry Informs National Dissemination.
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Measurement Properties of the CAPACITY Instrument to Assess Perceived Communication With the Health Care Team Among Care Partners of Patients With Cognitive Impairment.
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Measuring psychosocial risk in families caring for a child with cancer: the Psychosocial Assessment Tool (PAT2.0).
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Mechanisms Through Which a Family Caregiver Coaching Intervention Might Reduce Anxiety Among Children in Military Households.
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Mechanisms of change for a family intervention in Kenya: An Integrated Clinical and Implementation Mapping approach.
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Medical Specialty Board Parental, Caregiver, and Medical Leave Policy Updates After 2021 American Board of Medical Specialties Mandate.
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Medicare claims indicators of healthcare utilization differences after hospitalization for ischemic stroke: Race, gender, and caregiving effects.
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Mindfulness based stress reduction in people with Parkinson's disease and their care partners.
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Missed opportunities for timely diagnosis of pediatric lupus in South Africa: a qualitative study.
-
Multifamily group treatment for veterans with traumatic brain injury: what is the value to participants?
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Multiple Roles of Parental Caregivers of Children with Complex Life-Threatening Conditions: A Qualitative Descriptive Analysis.
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Multiple risk factors in the development of externalizing behavior problems: group and individual differences.
-
National randomized controlled trial of virtual house calls for Parkinson disease.
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Nausea and vomiting perspectives among children receiving moderate to highly emetogenic chemotherapy treatment.
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Needs of care partners of older Veterans with serious illness.
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Negative and positive experiences of caregiving among family caregivers of older blunt trauma patients.
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Neighborhood Commute to Work Times and Self-Reported Caregiver Health Behaviors and Food Access.
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Neighborhood characteristics moderate effects of caregiving on glucose functioning.
-
Neuropsychiatric symptoms and the risk of institutionalization and death: the aging, demographics, and memory study.
-
Neutrophil function in young and old caregivers.
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New or Worsening Symptoms and Signs in Community-Dwelling Persons with Dementia: Incidence and Relation to Use of Acute Medical Services.
-
Next Step for Global Adolescent and Young Adult Oncology: A Core Patient-Centered Outcome Set.
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No Hugs Allowed: Isolation and Inequity in North Carolina Long-term Services and Supports During COVID-19.
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Novel Questionnaires for Assessing Signs and Symptoms of Eosinophilic Esophagitis in Children.
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Nursing home care: exploring the role of religiousness in the mental health, quality of life and stress of formal caregivers.
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Objective burden, resources, and other stressors among informal cancer caregivers: a hidden quality issue?
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Older person behavioral and psychological symptoms (BPS) and functional limitations mediate the association between older person cognitive impairment and depressive symptoms in the caregiver.
-
Older spouses' perceptions of partners' chronic arthritis pain: implications for spousal responses, support provision, and caregiving experiences.
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Oncologist-patient-caregiver decision-making discussions in the context of advanced cancer in an Asian setting.
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Oncologists' responses to patient and caregiver negative emotions and patient perception of quality of communication: results from a multi-ethnic Asian setting.
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Oral adherence in adults with acute myeloid leukemia (AML): results of a mixed methods study.
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Orphan status, HIV risk behavior, and mental health among adolescents in rural Kenya.
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Pain communication in the context of osteoarthritis: patient and partner self-efficacy for pain communication and holding back from discussion of pain and arthritis-related concerns.
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Palliative Care Awareness Among Advanced Cancer Patients and Their Family Caregivers in Singapore.
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Palliative Care Issues in Amyotrophic Lateral Sclerosis: An Evidenced-Based Review.
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Palliative and End-of-Life Care for Patients With Hematologic Malignancies.
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Palliative care, Version 1.2014. Featured updates to the NCCN Guidelines.
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Parent Experience of Neonatal Encephalopathy.
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Parent experience of caring for neonates with seizures.
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Parent pain responses as predictors of daily activities and mood in children with juvenile idiopathic arthritis: the utility of electronic diaries.
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Parental Approach to the Prevention and Management of Fever and Pain Following Childhood Immunizations: A Survey Study.
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Parental understanding of infant health information: health literacy, numeracy, and the Parental Health Literacy Activities Test (PHLAT).
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Parenting-related stress and psychological distress in mothers of toddlers with autism spectrum disorders.
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Parents Are "Essential" Caregivers.
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Parents' experiences of managing their child's diabetes using an insulin pump: a qualitative study.
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Participant-centered adaptations in caregiver trials: strategies for managing confounds.
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Partnering to cope with pain: A pilot study of a caregiver-assisted pain coping skills intervention for patients with cognitive impairment and dementia.
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Pastoral care for the person with dementia.
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Patient and Caregiver Attitudes and Practices of Exercise in Candidates Listed for Liver Transplantation.
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Patient and Caregiver Opinions of Motivational Interviewing Techniques In Role-Played Palliative Care Conversations: A Pilot Study.
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Patient and informal caregivers' knowledge of heart failure: necessary but insufficient for effective self-care.
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Patient and physician attitudes regarding risk and benefit in streamlined development programmes for antibacterial drugs: a qualitative analysis.
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Patient predictors of caregiver burden, optimism, and pessimism in rheumatoid arthritis.
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Patient, Caregiver, and Nurse Preferences for Treatments for Bone Metastases from Solid Tumors.
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Patient, Caregiver, and Taxpayer Knowledge of Palliative Care and Views on a Model of Community-Based Palliative Care.
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Patients with cancer and their spouse caregivers. Perceptions of the illness experience.
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Patients' and caregivers' maximum acceptable risk of death for non-curative gene therapy to treat Duchenne muscular dystrophy.
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Patients, caregivers, and clinicians differ in performance status ratings: Implications for pediatric cancer clinical trials.
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Patterns and health effects of caring for people with dementia: the impact of changing cognitive and residential status.
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Pediatric to Adult Transition Literature: Scoping Review and Rheumatology Research Prioritization Survey Results.
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Perceived barriers and supports to accessing community-based services for Uganda's pediatric post-surgical population.
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Perceived burden and family functioning among informal caregivers of individuals living with schizophrenia in Tanzania: a cross-sectional study.
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Perceptions of patients' self-efficacy for managing pain and lung cancer symptoms: correspondence between patients and family caregivers.
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Perspectives on decision making amongst older people with end-stage renal disease and caregivers in Singapore: A qualitative study.
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Physician allocation of Medicare resources for patients with advanced cancer.
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Physician and Patient and Caregiver Health Attitudes and Their Effect on Medicare Resource Allocation for Patients With Advanced Cancer.
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Physician communication with family caregivers of long-term care residents at the end of life.
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Pilot Trial of a Combined Oncologist-Patient-Caregiver Communication Intervention in Singapore.
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Pilot study: individualized training for caregivers of hospitalized older veterans.
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Position statement of the American Association for Geriatric Psychiatry regarding principles of care for patients with dementia resulting from Alzheimer disease.
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Position statement: Policies to support family caregivers.
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Postoperative Pain Management in Children of Hispanic Origin: A Descriptive Cohort Study.
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Poststroke activity engagement in community dwellers: Association with illness perceptions and perceived environment.
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Pragmatic adaptations of telehealth-delivered caregiver coaching for children with autism in the context of COVID-19: Perspectives from the United States and South Africa.
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Predictors of HPV vaccination in the southern US: A survey of caregivers from 13 states.
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Predictors of Secondary Role Strains Among Spousal Caregivers of Older Adults With Functional Disability.
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Predictors of discharge from the VA Caregiver Support Program.
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Predictors of family violence in North Carolina following initial COVID-19 stay-at-home orders.
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Preferences versus practice: life-sustaining treatments in last months of life in long-term care.
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Preliminary Data from the Caring for Older Adults and Caregivers at Home (COACH) Program: A Care Coordination Program for Home-Based Dementia Care and Caregiver Support in a Veterans Affairs Medical Center.
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Preparing for the end of life: preferences of patients, families, physicians, and other care providers.
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Prevalence and predictors of HIV-related stigma among institutional- and community-based caregivers of orphans and vulnerable children living in five less-wealthy countries.
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Priorities when deciding on participation in early-phase gene therapy trials for Duchenne muscular dystrophy: a best-worst scaling experiment in caregivers and adult patients.
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Program preferences to reduce stress in caregivers of patients with brain tumors.
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Projecting the effects of long-term care policy on the labor market participation of primary informal family caregivers of elderly with disability: insights from a dynamic simulation model.
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Promoting a good death for persons with dementia in nursing facilities: family caregivers' perspectives.
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Prospective study of neuropsychologic testing and quality-of-life assessment of adults with primary malignant brain tumors.
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Protective and Unequal? Caregiver Presence During Pediatric Hospitalizations.
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Protocol for a mixed methods feasibility and implementation study of a community-based integrated care model for home-dwelling older adults: The INSPIRE project.
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Psychiatric symptomatology and disorders in caregivers of children with asthma.
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Psychologic interventions and lifestyle modifications for arthritis pain management.
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Psychological aspects of persistent pain: current state of the science.
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Psychological morbidity of Thai families of a person with schizophrenia.
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Psychological treatments delivered by community health workers in low-resource government health systems: effectiveness of group interpersonal psychotherapy for caregivers of children affected by nodding syndrome in Uganda.
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Psychological well-being of Chinese Immigrant adult-child caregivers: how do filial expectation, self-rated filial performance, and filial discrepancy matter?
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Psychophysiological mediators of caregiver stress and differential cognitive decline.
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Psychosocial Burden of Childhood Sickle Cell Disease on Caregivers in Kenya.
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Psychosocial stress moderates the relationship of cancer history with natural killer cell activity.
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Quality of life of patients with otitis media and caregivers: a multicenter study.
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Racial and Ethnic Differences in Communication Quality During Family-Centered Rounds.
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Racial and Ethnic Differences in Injury Prevention Behaviors Among Caregivers of Infants.
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Racial disparities in fifth-grade sun protection: Evidence from the Healthy Passages study.
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Randomized Pilot Trial of a Telephone Symptom Management Intervention for Symptomatic Lung Cancer Patients and Their Family Caregivers.
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Randomized trial of an uncertainty self-management telephone intervention for patients awaiting liver transplant.
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Ratings of personality change in patients being evaluated for memory disorders.
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Recommendations to Improve Health Outcomes Through Recognizing and Supporting Caregivers.
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Recommended scoring approach for the pediatric patient-reported outcomes version of the Common Terminology Criteria for Adverse Events.
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Recruitment and retention rates in behavioral trials involving patients and a support person: a systematic review.
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Recruitment of African-American pre-adolescent girls into an obesity prevention trial: the GEMS pilot studies.
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Regulating Together: Emotion Dysregulation Group Treatment for ASD Youth and Their Caregivers.
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Relation between informant-rated personality and clinician-rated depression in patients with memory disorders.
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Relationship between self-reported disability and caregiver hours.
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Religion and Caregiving for Orphans and Vulnerable Children: A Qualitative Study of Caregivers Across Four Religious Traditions and Five Global Contexts.
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Religious Coping Among Adults Caring for Family Members with Serious Mental Illness.
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Religious Involvement and Adaptation in Female Family Caregivers.
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Religious Involvement and Telomere Length in Women Family Caregivers.
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Religious views of the 'medical' rehabilitation model: a pilot qualitative study.
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Remembering the Calling - Where Patients and Caregivers Are Front and Center.
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Reminders of cancer risk and pain catastrophizing: relationships with cancer worry and perceived risk in women with a first-degree relative with breast cancer.
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Replicating an effective VA program to train and support family caregivers: a hybrid type III effectiveness-implementation design.
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Reported activities of daily living: agreement between elderly subjects with and without dementia and their caregivers.
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Research Priorities to Advance the Health and Health Care of Older Adults with Multiple Chronic Conditions.
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Resident challenges with daily life in Chinese long-term care facilities: A qualitative pilot study.
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Risk and resilience of well-being in caregivers of young children in response to the COVID-19 pandemic.
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Risk reconsidered: targets of violence in the social networks of people with serious psychiatric disorders.
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Role of caregiver factors in outpatient medical follow-up post-stroke: observational study in Singapore.
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Room for Improvement Remains in Food Consumption Patterns of Young Children Aged 2-4 Years.
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Rural-urban differences in preventable hospitalizations among community-dwelling veterans with dementia.
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Ruth's resolve: what Jesus' great-grandmother may teach about bioethics and care.
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SARS-CoV-2 vaccine acceptability among caregivers of childhood cancer survivors.
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Self-efficacy for managing pain, symptoms, and function in patients with lung cancer and their informal caregivers: associations with symptoms and distress.
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Serious physical illness as a stressor: effects on family use of medical services.
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Shared Decision-Making in Hematopoietic Stem Cell Transplantation for Sickle Cell Disease.
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Sharing the care of mechanical circulatory support: collaborative efforts of patients/caregivers, shared-care sites, and left ventricular assist device implanting centers.
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Short-Term Trajectories of Depressive Symptoms in Stroke Survivors and Their Family Caregivers.
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Short-term effects of comprehensive caregiver supports on caregiver outcomes.
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Simulating the impact of long-term care policy on family eldercare hours.
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Sleep quality varies as a function of 5-HTTLPR genotype and stress.
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Social issues of the Alzheimer's patient and family.
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Social service interventions for caregivers of patients with dementia: impact on health care utilization and expenditures.
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Specialized palliative care services are associated with improved short- and long-term caregiver outcomes.
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Spinal muscular atrophy type 1 quality of life.
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Spirituality and depression: a case study.
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Spirituality and psychological well-being: testing a theory of family interdependence among family caregivers and their elders.
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Spouse-assisted coping skills training in the management of knee pain in osteoarthritis: long-term followup results.
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Stakeholders' perspective on issues and challenges associated with care and treatment of aging-related cognitive impairment disorders in Singapore.
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Standing Up For My Sister.
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Stress and coping in caregivers of patients awaiting solid organ transplantation.
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Stroke Rehabilitation Use and Caregiver Psychosocial Health Profiles in Singapore: A Latent Profile Transition Analysis.
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Study protocol for a cohort study of patients with advanced heart failure in Singapore.
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Study protocol for a randomised controlled trial of a care partner assisted intervention to improve oral health of individuals with mild dementia.
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Supporting Family Caregivers of Older Americans.
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Supporting cancer family caregivers: How can frontline oncology clinicians help?
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Supportive approaches for Alzheimer disease.
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Surrogate assessment of coronary artery disease patients' functional capacity.
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Surviving critical illness: acute respiratory distress syndrome as experienced by patients and their caregivers.
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Systematic identification of family caregivers in health systems: Proposed solutions from a caregiver-focused research study.
-
Systematic review of financial burden assessment in cancer: Evaluation of measures and utility among adolescents and young adults and caregivers.
-
Systematic review of the effectiveness of non-pharmacological interventions to improve quality of life of people with dementia.
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Teaching elderly individuals on computer use.
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Technology and TBI: Perspectives of persons with TBI and their family caregivers on technology solutions to address health, wellness, and safety concerns.
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The "invisible caregiver": multicaregiving among diabetic African-American grandmothers.
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The Association of Self-esteem With Caregiving Demands, Coping, Burden, and Health Among Caregivers of Breast Cancer Patients: A Structural Equation Modeling Approach.
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The Behavior Rating Scale for Dementia of the Consortium to Establish a Registry for Alzheimer's Disease. The Behavioral Pathology Committee of the Consortium to Establish a Registry for Alzheimer's Disease.
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The Comprehensive Post-Acute Stroke Services (COMPASS) study: design and methods for a cluster-randomized pragmatic trial.
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The Effect of Support and Training for Family Members on Access to Outpatient Services for Veterans with Posttraumatic Stress Disorder (PTSD).
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The Experience of Caregivers Following a Moderate to Severe Traumatic Brain Injury Requiring ICU Admission.
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The Impact of Care Intensity and Work on the Mental Health of Family Caregivers: Losses and Gains.
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The Impact of Stigma on Community Reintegration of Veterans With Traumatic Brain Injury and the Well-Being of Their Caregivers.
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The Landscape of State Policies Supporting Family Caregivers as Aligned With the National Academy of Medicine Recommendations.
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The Patterns of Caregiving Activities for Family Caregivers of Older Adults in Hong Kong: An Exploratory Latent Class Analysis.
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The Relationship between Training and Mental Health among Caregivers of Individuals with Polytrauma.
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The Treatment of Behavioral and Psychological Symptoms of Dementia: Weighing Benefits and Risks.
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The association of acculturation and health literacy, numeracy and health-related skills in Spanish-speaking caregivers of young children.
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The associations between caregivers' psychosocial characteristics and caregivers' depressive symptoms in stroke settings: a cohort study.
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The burden of Parkinson's disease on society, family, and the individual.
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The burden of caring: drug users & their families.
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The caregiving environments provided to children by depressed mothers with or without an antisocial history.
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The effect of informal care on work and wages.
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The effect of spousal caregiving and bereavement on depressive symptoms.
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The effects of China's universal two-child policy.
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The experience of care partners of patients with Parkinson's disease psychosis.
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The experiences of older caregivers of cancer patients following hospital discharge.
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The feasibility and acceptability of a chaplain-led intervention for caregivers of seriously ill patients: A Caregiver Outlook pilot study.
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The frequency and troublesomeness of symptoms associated with Alzheimer's disease.
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The healthy families act: vital support for families of people with developmental disabilities.
-
The impact of a family skills training intervention among Burmese migrant families in Thailand: A randomized controlled trial.
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The impact of education on caregiver burden on two inpatient oncology units.
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The impact of goal adjustment and caregiver burden on psychological distress among caregivers of cancer patients.
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The impact of own and spouse's urinary incontinence on depressive symptoms.
-
The implications of out-of-pocket cost of cancer treatment in the USA: a critical appraisal of the literature.
-
The importance of context in early autism intervention: A qualitative South African study.
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The influence of neighborhood disadvantage and perceived disapproval on early substance use initiation.
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The nature and scope of stressful spousal caregiving relationships.
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The period of untreated psychosis before treatment initiation: a qualitative study of family members' perspectives.
-
The prevalence and process of pediatric HIV disclosure: A population-based prospective cohort study in Zimbabwe.
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The prevention of major depression in the elderly.
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The role of community-based and philanthropic organizations in meeting cancer patient and caregiver needs.
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The self-efficacy of family caregivers for helping cancer patients manage pain at end-of-life.
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The social context of gastrointestinal cancer pain: a preliminary study examining the relation of patient pain catastrophizing to patient perceptions of social support and caregiver stress and negative responses.
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The two voices of Alzheimer's: attitudes toward brain health by diagnosed individuals and support persons.
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The types of caregiving reactions experienced by the older spouse caregivers.
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Therapeutic Alliance between the Caregivers of Critical Illness Survivors and Intensive Care Unit Clinicians.
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There is a mismatch between the medicare benefit package and the preferences of patients with cancer and their caregivers.
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Three-year change in the wellbeing of orphaned and separated children in institutional and family-based care settings in five low- and middle-income countries.
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Training Health Care Practitioners to Include Family Caregivers With Web-Based Learning Modules.
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Trajectories of caregiving time provided by wives to their husbands with dementia.
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Trajectories of positive aspects of caregiving among family caregivers of stroke-survivors: the differential impact of stroke-survivor disability.
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Transactional relations between caregiving stress, executive functioning, and problem behavior from early childhood to early adolescence.
-
Transitional Care Partners: a hospital-to-home support for older adults and their caregivers.
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Transitional care after hospitalization for acute stroke or myocardial infarction: a systematic review.
-
Transitional care from skilled nursing facilities to home: study protocol for a stepped wedge cluster randomized trial.
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Transitions of care in heart failure: a scientific statement from the American Heart Association.
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Trauma-Directed Interaction (TDI): An Adaptation to Parent-Child Interaction Therapy for Families with a History of Trauma.
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Trauma-informed care for youth suicide prevention: A qualitative analysis of caregivers' perspectives.
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Treating excess disability among cognitively impaired nursing home residents.
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Triadic agreement about advanced cancer treatment decisions: Perceptions among patients, families, and oncologists.
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Triadic treatment decision-making in advanced cancer: a pilot study of the roles and perceptions of patients, caregivers, and oncologists.
-
Understanding factors that influence the demand for dialysis among elderly in a multi-ethnic Asian society.
-
Understanding on the association between informal caregiver characteristics and cognitive function of adults with cancer: a scoping review protocol.
-
Understanding the financial and psychological impact of employment disruption among caregivers of pediatric HSCT recipients: a mixed methods analysis.
-
Understanding the needs of people with ALS: a national survey of patients and caregivers.
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Understanding the relative importance of preserving functional abilities in Alzheimer's disease in the United States and Germany.
-
Unique Care Needs of People with Dementia and Their Caregivers during Transitions from Skilled Nursing Facilities to Home and Assisted Living: A Qualitative Study.
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Unmet expectations of medications and care providers among patients with heart failure assessed to be poorly adherent: results from the Chronic Heart Failure Intervention to Improve MEdication Adherence (CHIME) study.
-
Unmet needs and depression among carers of people newly diagnosed with cancer.
-
Unpaid Caregiving Roles and Sleep Among Women Working in Nursing Homes: A Longitudinal Study.
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Untangling the relative contribution of maltreatment severity and frequency to type of behavioral outcome in foster youth.
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Use of motivational techniques to enhance unpaid caregiver engagement in a tailored skills training intervention.
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Use of tangible, educational and psychological support services among Chinese American dementia caregivers.
-
Utilization and Cost Effects of the VHA Caring for Older Adults and Caregivers at Home (COACH) Program.
-
Utilization of Text Messages to Supplement Rounding Communication: a Randomized Feasibility Study.
-
Validation of the Observer-Reported Communication Ability (ORCA) Measure for Individuals With Angelman Syndrome.
-
Validation of the caregiver Pediatric Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events measure.
-
Validity and Reliability of the Positive Aspects of Caregiving (PAC) Scale and Development of Its Shorter Version (S-PAC) Among Family Caregivers of Older Adults.
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Validity and reliability of the Caregiver Reaction Assessment scale among primary informal caregivers for older persons in Singapore.
-
Validity of evidence-derived criteria for reactive attachment disorder: indiscriminately social/disinhibited and emotionally withdrawn/inhibited types.
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Variation in caregiver perceptions of teamwork climate in labor and delivery units.
-
Veterans Health Administration Models of Community-Based Long-Term Care: State of the Science.
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Victimization and Adversity in Child Welfare Involved Youth: The Cumulative Influence on Child and Caregiver Reported Behavioral Health Symptoms.
-
Video-Enhanced Care Management for Medically Complex Older Adults with Cognitive Impairment.
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Video-based coping skills to reduce health risk and improve psychological and physical well-being in Alzheimer's disease family caregivers.
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What is a Good Death? A Choice Experiment on Care Indicators for Patients at End of Life.
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What is the role of friends when contributing care at the end of life? Findings from an Australian population study.
-
What's in a manner of speaking? Children's sensitivity to partner-specific referential precedents.
-
When "the family" is not one voice: conflict in caregiving families.
-
When Should Patients Be Involved in Cardiovascular Clinical Trial Design?: Always, Early, and Often.
-
When parents have a history of conduct disorder: how is the caregiving environment affected?
-
Where Are We and What Shall We Do Next? A Qualitative Study of the Quality of Home Care in Shanghai, China.
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Willingness to Undergo a Risky Treatment to Improve Cognition Among Persons With Cognitive Impairment Who Received an Amyloid PET Scan.
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Young caregivers in the end-of-life setting: a population-based profile of an emerging group.
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Keywords of People
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Albrecht, Tara,
Associate Professor in the School of Nursing,
School of Nursing
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Anderson, Ruth A.,
Professor Emerita in the School of Nursing,
School of Nursing
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Bettger, Janet Prvu,
Adjunct Associate in the Department of Orthopaedic Surgery,
Duke Science & Society
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Boucher, Nathan Adam,
Associate Research Professor in the Sanford School of Public Policy,
Medicine, Geriatrics
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Grambow, Steven C.,
Associate Professor of Biostatistics & Bioinformatics,
Biostatistics & Bioinformatics
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Lee, Walter T,
Professor of Head and Neck Surgery & Communication Sciences,
Radiation Oncology
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McConnell, Eleanor Schildwachter,
Associate Professor in the School of Nursing,
School of Nursing
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Milano, Carmelo Alessio,
Joseph W. and Dorothy W. Beard Distinguished Professor of Experimental Surgery,
Surgery, Cardiovascular and Thoracic Surgery
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Ostbye, Truls,
Professor of Family Medicine and Community Health,
Family Medicine and Community Health
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Schanberg, Laura Eve,
Professor of Pediatrics,
Pediatrics, Rheumatology
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Yancy Jr., William Samuel,
Professor of Medicine,
Medicine, General Internal Medicine
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Zafar, Syed Yousuf,
Adjunct Professor in the Department of Medicine,
Duke Science & Society
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Zullig, Leah L,
Professor in Population Health Sciences,
Medicine, General Internal Medicine