All Stories

  1. Which website should health care providers recommend to informal caregivers
  2. Self-management across chronic diseases: Targeting education and support needs
  3. The direct and indirect financial costs of informal cancer care: A scoping review
  4. An evaluation of the suitability, readability, and quality of online resources for the self-management of depression
  5. Self-management support in primary care is associated with improvement in patient activation
  6. Developing education materials for caregivers of culturally and linguistically diverse patients: Insights from a qualitative analysis of caregivers' needs, access and understanding of information
  7. Identifying priorities for cancer caregiver interventions: protocol for a three-round modified Delphi study
  8. Pilot Study of a Transitional Intervention for Family Caregivers of Older Adults
  9. The “sphere of care”: A qualitative study of colorectal cancer patient and caregiver experiences of support within the cancer treatment setting
  10. Finding My Way: results of a multicentre RCT evaluating a web-based self-guided psychosocial intervention for newly diagnosed cancer survivors
  11. A fertility needs assessment survey of male cancer patients
  12. A protocol for an updated and expanded systematic mixed studies review of fear of cancer recurrence in families and caregivers of adults diagnosed with cancer
  13. Adaptation of Coping Together - a self-directed coping skills intervention for patients and caregivers in an outpatient hematopoietic stem cell transplantation setting: a study protocol
  14. Unmet needs of family caregivers of hospitalized older adults preparing for discharge home
  15. Priorities for caregiver research in cancer care: an international Delphi survey of caregivers, clinicians, managers, and researchers
  16. “It sort of hit me like a baseball bat between the eyes”: a qualitative study of the psychosocial experiences of mesothelioma patients and carers
  17. Relationships between supportive care needs and perceived burden in breast cancer survivor-caregiver dyads
  18. Beyond using composite measures to analyze the effect of unmet supportive care needs on caregivers' anxiety and depression
  19. The Effectiveness of Self-Management Interventions for Individuals with Low Health Literacy and/or Low Income: A Descriptive Systematic Review
  20. PROMIS depression measures perform similarly to legacy measures relative to a structured diagnostic interview for depression in cancer patients
  21. A systematic review and meta-analysis of written self-administered psychosocial interventions among adults with a physical illness
  22. Routine assessment of unmet needs in individuals with advanced cancer and their caregivers: A qualitative study of the palliative care needs assessment tool (PC-NAT)
  23. Impact of informal caregiving on older adults’ physical and mental health in low-income and middle-income countries: a cross-sectional, secondary analysis based on the WHO’s Study on global AGEing and adult health (SAGE)
  24. Phase II trial of a depression self-care intervention for adult cancer survivors
  25. Trajectories of mental and physical functioning among spouse caregivers of cancer survivors over the first five years following the diagnosis
  26. Perceptions of cancer of unknown primary site: a national survey of Australian medical oncologists
  27. Why sample selection matters in exploratory factor analysis: implications for the 12-item World Health Organization Disability Assessment Schedule 2.0
  28. Uptake and adherence to an online intervention for cancer-related distress: older age is not a barrier to adherence but may be a barrier to uptake
  29. La gestion de la dépression chez les aînés et leurs aidants naturels : résultats d’un programme de recherche au Québec
  30. Study Protocol: Evaluation of a DVD intervention designed to meet the informaton needs of patients with head and neck cancer and their partner, carer and families
  31. Online Health Information Regarding Male Infertility: An Evaluation of Readability, Suitability, and Quality
  32. A Descriptive Systematic Review of Physical Activity Interventions for Caregivers: Effects on Caregivers’ and Care Recipients’ Psychosocial Outcomes, Physical Activity Levels, and Physical Health
  33. Baseline Psychological Treatment Reduces the Effect of Coaching in a Randomised Trial of a Depression Self-Care Intervention
  34. Activation and Self-Efficacy in a Randomized Trial of a Depression Self-Care Intervention
  35. Burnout and the provision of psychosocial care amongst Australian cancer nurses
  36. Recovering function and surviving treatments are primary motivators for health behavior change in patients with head and neck cancer: Qualitative focus group study
  37. Integrative Review of the Supportive Care Needs of Asian and Caucasian Women with Breast Cancer
  38. A Qualitative Investigation of Health Care Professionals’, Patients’ and Partners’ Views on Psychosocial Issues and Related Interventions for Couples Coping with Cancer
  39. A pilot, multisite, randomized controlled trial of a self-directed coping skills training intervention for couples facing prostate cancer: accrual, retention, and data collection issues
  40. Couples coping with cancer: exploration of theoretical frameworks from dyadic studies
  41. Measuring appraisal during advanced cancer: Psychometric testing of the appraisal of caregiving scale
  42. Finding My Way: protocol of a randomised controlled trial evaluating an internet self-help program for cancer-related distress
  43. Wellbeing during Active Surveillance for localised prostate cancer: A systematic review of psychological morbidity and quality of life
  44. Cross-sectional relationships between dyadic coping and anxiety, depression, and relationship satisfaction for patients with prostate cancer and their spouses
  45. Using Rasch analysis to examine the distress thermometer’s cut-off scores among a mixed group of patients with cancer
  46. “You need something like this to give you guidelines on what to do”: patients' and partners' use and perceptions of a self-directed coping skills training resource
  47. Uptake and attrition in couple-based interventions for cancer: perspectives from the literature
  48. A parallel-group, randomised controlled trial of a multimedia, self-directed, coping skills training intervention for patients with cancer and their partners: design and rationale
  49. Physical, Psychosocial, Relationship, and Economic Burden of Caring for People With Cancer: A Review
  50. A systematic review of internet-based self-help therapeutic interventions to improve distress and disease-control among adults with chronic health conditions
  51. The ABC of Vitamin D: A Qualitative Study of the Knowledge and Attitudes Regarding Vitamin D Deficiency amongst Selected Population Groups
  52. A Rasch analysis of the Hospital Anxiety and Depression Scale (HADS) among cancer survivors.
  53. The incremental utility of callous-unemotional traits and conduct problems in predicting aggression and bullying in a community sample of boys and girls.
  54. Some things change, some things stay the same: a longitudinal analysis of cancer caregivers' unmet supportive care needs
  55. The unmet needs of partners and caregivers of adults diagnosed with cancer: a systematic review
  56. Distressed Partners and Caregivers Do Not Recover Easily: Adjustment Trajectories Among Partners and Caregivers of Cancer Survivors
  57. Walking a mile in their shoes: anxiety and depression among partners and caregivers of cancer survivors at 6 and 12 months post-diagnosis
  58. A pilot randomized controlled trial of the feasibility of a self-directed coping skills intervention for couples facing prostate cancer: Rationale and design
  59. Rasch analysis of the Mini-Mental Adjustment to Cancer Scale (mini-MAC) among a heterogeneous sample of long-term cancer survivors: A cross-sectional study
  60. The unfulfilled promise: a systematic review of interventions to reduce the unmet supportive care needs of cancer patients
  61. Measuring psychological outcomes following pediatric intensive care unit hospitalization: Psychometric analysis of the Childrenʼs Critical Illness Impact Scale
  62. Mothers’ experiences of a Touch and Talk nursing intervention to optimise pain management in the PICU: A qualitative descriptive study
  63. The supportive care needs survey for partners and caregivers of cancer survivors: development and psychometric evaluation
  64. An In-depth Exploration of Information-Seeking Behavior Among Individuals With Cancer
  65. An In-depth Exploration of Information-Seeking Behavior Among Individuals With Cancer
  66. Combining individual interviews and focus groups to enhance data richness
  67. Health Information—Seeking Behavior