| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1029105214 |
| P356 | DOI | 10.1007/S00520-012-1466-Z |
| P698 | PubMed publication ID | 22531878 |
| P2093 | author name string | Mogens Groenvold | |
| Lone Ross | |||
| Morten Aagaard Petersen | |||
| Anna Thit Johnsen | |||
| Line Lund | |||
| Louise Hyldborg Lundstrøm | |||
| P2860 | cites work | The Measurement of Observer Agreement for Categorical Data | Q26778373 |
| Teaching family carers about home-based palliative care: final results from a group education program | Q30228091 | ||
| Qualitative description - the poor cousin of health research? | Q33483038 | ||
| A systematic review of psychosocial interventions for family carers of palliative care patients | Q33650436 | ||
| The unmet supportive care needs of patients with cancer. Supportive Care Review Group | Q33807741 | ||
| Whatever happened to qualitative description? | Q34001833 | ||
| Burden and depression among caregivers of patients with cancer at the end of life | Q34226599 | ||
| What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. | Q35070569 | ||
| Palliative care: views of patients and their families | Q35170035 | ||
| Psychological distress in spouses of men treated for early-stage prostate carcinoma | Q37029312 | ||
| A narrative review of interventions to support family carers who provide physical care to family members with cancer. | Q37464357 | ||
| Validation of the EORTC QLQ-C30 quality of life questionnaire through combined qualitative and quantitative assessment of patient-observer agreement | Q42657927 | ||
| Family members of cancer patients: Needs, quality of life and symptoms of anxiety and depression | Q44838459 | ||
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| Using method triangulation to validate a new instrument (CPWQ-com) assessing cancer patients' satisfaction with communication. | Q50517238 | ||
| What makes grief difficult? Perspectives from bereaved family caregivers and healthcare providers of advanced cancer patients. | Q50665901 | ||
| Which carers of family members at the end of life need more support from health services and why? | Q50709383 | ||
| Advanced Palliative Home Care: Next-of-Kin's Perspective | Q50767385 | ||
| Benefits of training family caregivers on experiences of closure during end-of-life care. | Q51758484 | ||
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| A Coefficient of Agreement for Nominal Scales | Q57167717 | ||
| Are different groups of cancer patients offered rehabilitation to the same extent? A report from the population-based study “The Cancer Patient’s World” | Q62106279 | ||
| Patient sociodemographic characteristics as predictors of satisfaction with medical care: a meta-analysis | Q68412842 | ||
| Spouse adjustment to cancer surgery: distress and coping responses | Q68729760 | ||
| High agreement but low kappa: I. The problems of two paradoxes | Q68803935 | ||
| The impact of cancer on key relatives: a comparison of relative and patient concerns | Q70836306 | ||
| Patient satisfaction: a review of issues and concepts | Q74109497 | ||
| The correlation between coping strategies, doctor-patient/spouse relationships and psychological distress among women cancer patients and their spouses | Q79899537 | ||
| P433 | issue | 12 | |
| P304 | page(s) | 3211-3220 | |
| P577 | publication date | 2012-04-25 | |
| P1433 | published in | Supportive Care in Cancer | Q15766919 |
| P1476 | title | Using mixed methods to assess how cancer patients' needs in relation to their relatives are met in the Danish health care system: a report from the population-based study "The Cancer Patient's World". | |
| P478 | volume | 20 |
| Q47319251 | Family functioning and perceived support from nurses during cancer treatment among Danish and Australian patients and their families. |
| Q60504415 | Outcome of Supportive Talks in a Hospital Setting: Insights from Cancer Patients and Their Relatives |
| Q39406380 | Storytelling as part of cancer rehabilitation to support cancer patients and their relatives |
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