| Meaning of life, representation of death, and their association with psychological distress |
11 |
| The influence of psychological factors on the burden of caregivers of patients with advanced cancer: Resiliency and caregiver burden |
11 |
| Virtual reality as a distraction technique for pain and anxiety among patients with breast cancer: A randomized control trial |
9 |
| Patients with advanced cancer and depression report a significantly higher symptom burden than non-depressed patients |
8 |
| Postgraduate palliative care education for all healthcare providers in Europe: Results from an EAPC survey |
8 |
| Bereavement support standards and bereavement care pathway for quality palliative care |
8 |
| A scoping review of palliative care for persons with severe persistent mental illness |
8 |
| An open trial of meaning-centered grief therapy: Rationale and preliminary evaluation |
8 |
| Sleep problems in breast cancer survivors 1-10 years posttreatment |
7 |
| Methods for overcoming barriers in palliative care for ethnic/racial minorities: a systematic review |
6 |
| A cross-sectional pilot study of compassion fatigue, burnout, and compassion satisfaction in pediatric palliative care providers in the United States |
6 |
| From Barriers to Assets: Rethinking factors impacting advance care planning for African Americans |
6 |
| Supporting wellbeing in motor neurone disease for patients, carers, social networks, and health professionals: A scoping review and synthesis |
5 |
| Personalized and yet standardized: An informed approach to the integration of bereavement care in pediatric oncology settings |
5 |
| Optimism and quality of life in patients with heart failure |
5 |
| The effects of psychological meaning-centered therapies on quality of life and psychological stress: A metaanalysis |
5 |
| Efficacy of a written prayer technique on the anxiety of mothers of children with cancer |
5 |
| Dyadic psychological intervention for patients with cancer and caregivers in home-based specialized palliative care: The Domus model |
5 |
| Addressing religion and spirituality in the intensive care unit: A survey of clinicians |
5 |
| State of advance care planning research: A descriptive overview of systematic reviews |
5 |
| Insecure attachment predicts depression and death anxiety in advanced cancer patients |
5 |
| Barriers and facilitators to implementing the commission on cancer's distress screening program standard |
4 |
| Researching children's perspectives in pediatric palliative care: A systematic review and meta-summary of qualitative research |
4 |
| Spiritual care training in healthcare: Does it really have an impact? |
4 |
| Improving the Medical Assistance in Dying (MAID) process: A qualitative study of family caregiver perspectives |
4 |
| The care experiences of patients who die in residential hospice: A qualitative analysis of the last three months of life from the views of bereaved caregivers |
4 |
| Training for awareness of one's own spirituality: A key factor in overcoming barriers to the provision of spiritual care to advanced cancer patients by doctors and nurses |
4 |
| The emergence of personal growth amongst healthcare professionals who care for dying children |
4 |
| A scoping research literature review to assess the state of existing evidence on the bad death |
4 |
| Wernicke encephalopathy without delirium in patients with cancer |
4 |
| Palliative care education in Latin America: A systematic review of training programs for healthcare professionals |
4 |
| We never speak about death. Healthcare professionals' views on palliative care for inpatients in Tanzania: A qualitative study |
4 |
| Perspectives of patients, close relatives, nurses, and physicians on end-of-life medication management |
4 |
| Subsyndromal delirium in the intensive care setting: Phenomenological characteristics and discrimination of subsyndromal delirium versus no and full-syndromal delirium |
3 |
| Meaning-centered psychotherapy integrated with elements of compassion: A pilot study to assess feasibility and utility |
3 |
| Dignity in cancer patients with a life expectancy of a few weeks. Implementation of the factor structure of the Patient Dignity Inventory and dignity assessment for a patient-centered clinical intervention: A cross-sectional study |
3 |
| Post-intensive care syndrome symptoms and health-related quality of life in family decision-makers of critically ill patients |
3 |
| Trajectories of caregiver burden in families of adult cystic fibrosis patients |
3 |
| Sleep-wake difficulties in community-dwelling cancer patients receiving palliative care: subjective and objective assessment |
3 |
| Cancer pain management needs and perspectives of patients from Chinese backgrounds: a systematic review of the Chinese and English literature |
3 |
| Decisional control preferences of patients with advanced cancer receiving palliative care |
3 |
| The predictive value of symptoms for anxiety in hospice inpatients with advanced cancer |
3 |
| Early detection and successful treatment of Wernicke's encephalopathy in outpatients without the complete classic triad of symptoms who attended a psycho-oncology clinic |
3 |
| Family care conferences in long-term care: Exploring content and processes in end-of-life communication |
3 |
| Meaning and Purpose (MaP) therapy II: Feasibility and acceptability from a pilot study in advanced cancer |
3 |
| Association between burnout and cortisol secretion, perceived stress, and psychopathology in palliative care unit health professionals |
3 |
| Association between family satisfaction and caregiver burden in cancer patients receiving outreach palliative care at home |
3 |
| Subclinical thiamine deficiency in patients with abdominal cancer |
3 |
| The experience of informal caregivers of patients with motor neurone disease: A thematic synthesis |
3 |
| A conceptual model: Redesigning how we provide palliative care for patients with chronic obstructive pulmonary disease |
3 |
