Professional-Family Relations
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Subject Areas on Research
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"Let him speak:" a descriptive qualitative study of the roles and behaviors of family companions in primary care visits among older adults with cognitive impairment.
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A Person-Centered, Registry-Based Learning Health System for Palliative Care: A Path to Coproducing Better Outcomes, Experience, Value, and Science.
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A Pilot Randomized Trial of an Interactive Web-based Tool to Support Surrogate Decision Makers in the Intensive Care Unit.
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A commentary: the role of religion and spirituality at the end of life.
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A parent-based intervention to reduce sexual risk behavior in early adolescence: building alliances between physicians, social workers, and parents.
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Adaptive leadership framework for chronic illness: framing a research agenda for transforming care delivery.
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Adaptive leadership: a novel approach for family decision making.
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Afterword: Giving good advice: it is not what doctors say, but how they say it.
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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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An Integrative Review of Communication Between Parents and Nurses of Hospitalized Technology-Dependent Children
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An exploratory study of end-of-life prognostic communication needs as reported by widowed fathers due to cancer.
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Assessment of parent understanding in conferences for critically ill neonates.
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Autopsy and grief: a case of transformative postmortem examination.
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Beyond the First Wave: Consequences of COVID-19 on High-Risk Infants and Families.
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Cardiac care for older adults. Time for a new paradigm.
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Caring for Children With Medical Complexity With the Emergency Information Form.
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Changing times, changing opinions: history informing the family presence debate.
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Characterizing the Language Used to Discuss Death in Family Meetings for Critically Ill Infants.
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Communicating With Patients--The Other Side of the Conversation.
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Communicating prognosis with parents of critically ill infants: direct observation of clinician behaviors.
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Communication Challenges in Neonatal Encephalopathy.
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Communication and control: parent, child, and health care professional interactions during painful procedures
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Continuity of medical care, health insurance, and nonmedical advice in the first 3 years of life.
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Dealing with "Difficult" Patients and Families: Making a Case for Trauma-informed Care in the Intensive Care Unit.
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Decision Making for Infants With Neurologic Conditions.
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Developing a Research Agenda for Integrating Palliative Care into Critical Care and Pulmonary Practice To Improve Patient and Family Outcomes.
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Developing the family support tool: An interactive, web-based tool to help families navigate the complexities of surrogate decision making in ICUs.
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Evaluating cost-effectiveness of preevaluation client contacts.
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Examining clinical judgment in an adaptive intervention design: The fast track program.
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Examining the context and helpfulness of family companion contributions to older adults' primary care visits.
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Exploring the vagueness of Religion & Spirituality in complex pediatric decision-making: a qualitative study.
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Facilitators Associated With Building and Sustaining Therapeutic Alliance in Advanced Pediatric Cancer.
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Family-Centered Care for Children and Families Impacted by Neonatal Seizures: Advice From Parents.
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Feasibility and acceptability of the TALK social worker intervention to improve live kidney transplantation.
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Finding your way through EOL challenges in the ICU using Adaptive Leadership behaviours: A qualitative descriptive case study.
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Guidelines for Family-Centered Care in the Neonatal, Pediatric, and Adult ICU.
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Health Care Professionals' Responses to Religious or Spiritual Statements by Surrogate Decision Makers During Goals-of-Care Discussions.
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How healthcare provider talk with parents of children following severe traumatic brain injury is perceived in early acute care.
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Identifying and addressing barriers to African American and non-African American families' discussions about preemptive living related kidney transplantation.
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Implementation of a clinical study of a pain management program for pediatric oncology patients
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Implementation of condition help: family teaching and evaluation of family understanding.
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Improving communication and recall of information in paediatric diabetes consultations: a qualitative study of parents' experiences and views.
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Initial evaluation of suspected dementia. Asking the right questions.
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Insights into patient and family-centered care through the hospital experiences of parents.
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Integration of Parent and Nurse Perspectives of Communication to Plan Care for Technology Dependent Children: The Theory of Shared Communication.
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Management of patients with Parkinson disease.
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Management of terminal cancer in elderly patients.
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Managing the patient with dementia.
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Modifiable elements of ICU supportive care and communication are associated with surrogates' PTSD symptoms.
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Neurologic Outcome After Prematurity: Perspectives of Parents and Clinicians.
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No heroic measures: how soon is too soon to stop?
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No question too small: development of a question prompt list for parents of critically ill infants.
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Nurses' Role in Providing Comprehensive Communication, Prognostication, and Palliative Care During the COVID-19 Pandemic.
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Nursing strategies to support family members of ICU patients at high risk of dying.
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Older adults and their families in a community mental health center: strategies for intervention.
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One intensive care nursery's experience with enhancing patient safety.
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Palliative and End-of-Life Care for Newborns and Infants: From the National Association of Neonatal Nurses.
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Parent experience of caring for neonates with seizures.
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Parent perceptions of early prognostic encounters following children's severe traumatic brain injury: 'locked up in this cage of absolute horror'.
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Parent-Based Sexual Health Promotion and Sexually Transmitted Infections Prevention for Youth.
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Parent-provider communication during hospitalization
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Parental Perceptions of Displayed Patient Data in a PICU: An Example of Unintentional Empowerment.
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Patient and Family Engagement in Critical Illness.
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Patient-Family Agenda Setting for Primary Care Patients with Cognitive Impairment: the SAME Page Trial.
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Patient/Family Education for Newly Diagnosed Pediatric Oncology Patients.
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Pediatric Traumatic Brain Injury: Families and Healthcare Team Interaction Trajectories During Acute Hospitalization.
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Pediatric brain tumor patients: their parents' perceptions of the hospital experience.
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Physician attire in the intensive care unit in Japan influences visitors' perception of care.
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Physician communication with family caregivers of long-term care residents at the end of life.
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Pilot study: individualized training for caregivers of hospitalized older veterans.
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Policy to practice: increased family presence and the impact on patient- and family-centered care adoption.
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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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Primary care providers' self-efficacy and outcome expectations for childhood obesity counseling.
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Processing Information After a Child's Cancer Diagnosis-How Parents Learn.
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Prognostic Communication Between Oncologists and Parents of Children With Advanced Cancer.
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Prognostic Discussion for Infants with Neurologic Conditions: Qualitative Analysis of Family Conferences.
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Provider experience and attitudes toward family presence during resuscitation procedures.
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Questions & answers: Integrating academics in the context of eating disorder treatment.
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Role of Social Workers in Family Conferences for Critically Ill Infants.
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Satisfaction With Communication in Primary Care for Spanish-Speaking and English-Speaking Parents.
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Special clinical problems in the management of psychiatric inpatients.
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Spiritual Care Providers and Goals-of-Care Discussions--Reply.
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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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Surrogates' perceptions about feeding tube placement decisions.
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The Voice of Surrogate Decision-Makers. Family Responses to Prognostic Information in Chronic Critical Illness.
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The clinical librarian and the patient: report of a project at McMaster University Medical Centre.
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The effectiveness of a brief intervention for emotion-focused nurse-parent communication
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The family and type 2 diabetes: a framework for intervention.
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The theory of shared communication: how parents of technology-dependent children communicate with nurses on the inpatient unit
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Understanding Effective Delivery of Patient and Family Education in Pediatric OncologyA Systematic Review From the Children's Oncology Group [Formula: see text]
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When Words Are All We Have.
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Why Parents Seek Care for Acute Illness in the Clinic or the ED: The Role of Health Literacy.
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Withholding medical treatment from the severely demented patient. Decisional processes and cost implications.
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Working with the family of a critically ill child
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Young worker safety in construction: do family ties and workgroup size affect hazard exposures and safety practices?
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Keywords of People