Understanding the support needs of family members of people undergoing chemotherapy: A longitudinal qualitative study.

[1]  A. Wilder Smith,et al.  The Characteristics of Informal Cancer Caregivers in the United States. , 2019, Seminars in oncology nursing.

[2]  C. Wirtz,et al.  Supportive Care Needs in Glioma Patients and Their Caregivers in Clinical Practice: Results of a Multicenter Cross-Sectional Study , 2018, Front. Neurol..

[3]  A. Charalambous,et al.  How family caregivers of cancer patients manage symptoms at home: A systematic review. , 2018, International journal of nursing studies.

[4]  R. Epstein,et al.  Family caregiver descriptions of stopping chemotherapy and end-of-life transitions , 2018, Supportive Care in Cancer.

[5]  L. Calman,et al.  A revised model for coping with advanced cancer. Mapping concepts from a longitudinal qualitative study of patients and carers coping with advanced cancer onto Folkman and Greer's theoretical model of appraisal and coping , 2018, Psycho-oncology.

[6]  Scott J. Fitzpatrick,et al.  ‘Shadowing’ as a management strategy for chemotherapy outpatient primary support persons , 2017, Scandinavian journal of caring sciences.

[7]  V. Marconi,et al.  Code Saturation Versus Meaning Saturation , 2017, Qualitative health research.

[8]  L. Calman,et al.  Coping Well with Advanced Cancer: A Serial Qualitative Interview Study with Patients and Family Carers , 2017, PloS one.

[9]  G. Hubbard,et al.  From an illusion of certainty into a reality of uncertainty: A longitudinal qualitative study of how people affected by laryngeal cancer use information over time. , 2016, European journal of oncology nursing : the official journal of European Oncology Nursing Society.

[10]  C. Mihalopoulos,et al.  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 , 2016, Supportive Care in Cancer.

[11]  S. Morris,et al.  Estimating the cost of caring for people with cancer at the end of life: A modelling study , 2015, Palliative medicine.

[12]  H. Friederich,et al.  When do we need to care about the caregiver? Supportive care needs, anxiety, and depression among informal caregivers of patients with cancer and cancer survivors , 2015, Cancer.

[13]  G. Robert,et al.  Enhancing the experience of carers in the chemotherapy outpatient setting: an exploratory randomised controlled trial to test impact, acceptability and feasibility of a complex intervention co-designed by carers and staff , 2015, Supportive Care in Cancer.

[14]  H. Wong,et al.  The impact of a new acute oncology service in acute hospitals: experience from the Clatterbridge Cancer Centre and Merseyside and Cheshire Cancer Network. , 2013, Clinical medicine.

[15]  A. Richardson,et al.  Informal carers' experiences and needs when supporting patients through chemotherapy: a mixed method study. , 2013, European journal of cancer care.

[16]  P. McElduff,et al.  Some things change, some things stay the same: a longitudinal analysis of cancer caregivers' unmet supportive care needs , 2013, Psycho-oncology.

[17]  R. McCorkle,et al.  Factors associated with depressive symptoms in cancer family caregivers of patients receiving chemotherapy , 2013, Supportive Care in Cancer.

[18]  A. Molassiotis,et al.  Developing longitudinal qualitative designs: lessons learned and recommendations for health services research , 2013, BMC Medical Research Methodology.

[19]  W. Breitbart,et al.  Care for the cancer caregiver: A systematic review , 2012, Palliative and Supportive Care.

[20]  B. Given,et al.  The cancer family caregiving experience: an updated and expanded conceptual model. , 2012, European journal of oncology nursing : the official journal of European Oncology Nursing Society.

[21]  P. Potter,et al.  Psychosocial aspects of caregiving: perceptions of cancer patients and family caregivers , 2012, Supportive Care in Cancer.

[22]  A. Sheikh,et al.  Archetypal trajectories of social, psychological, and spiritual wellbeing and distress in family care givers of patients with lung cancer: secondary analysis of serial qualitative interviews , 2010, BMJ : British Medical Journal.

[23]  Carl May,et al.  We need minimally disruptive medicine , 2009, BMJ : British Medical Journal.

[24]  G. Humphris,et al.  Fear of recurrence and psychological distress in head and neck cancer patients and their carers , 2009, Psycho-oncology.

[25]  J. Ussher,et al.  Evaluating the efficacy of psycho-social interventions for informal carers of cancer patients: a systematic review of the research literature , 2009 .

[26]  P. Ward-smith,et al.  When a Family Member Has a Malignant Brain Tumor: The Caregiver Perspective , 2008, The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses.

[27]  D. Zwahlen,et al.  Quality of life and dyadic adjustment in oral cancer patients and their female partners. , 2008, European journal of cancer care.

[28]  Trevor Murrells,et al.  Patients' supportive care needs beyond the end of cancer treatment: a prospective, longitudinal survey. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[29]  K. Sullivan,et al.  What about the carers?: Exploring the experience of caregivers in a chemotherapy day hospital setting. , 2006, European journal of oncology nursing : the official journal of European Oncology Nursing Society.

[30]  Michael A Richards,et al.  Advanced breast cancer patients' perceptions of decision making for palliative chemotherapy. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[31]  Dennis F. Moore,et al.  Cancer patients' expectations of experiencing treatment‐related side effects , 2004, Cancer.

[32]  J. Addington-hall,et al.  Perspectives on symptom control in patients receiving community palliative care , 2003, Palliative medicine.

[33]  F. Baker,et al.  Family caregivers and indicators of cancer-related distress , 2003, Psychology, health & medicine.

[34]  S. Aranda,et al.  Home Caregivers of the Person With Advanced Cancer: AN AUSTRALIAN PERSPECTIVE , 2001, Cancer nursing.

[35]  V. Mock,et al.  Caregiver responses and needs. An ambulatory bone marrow transplant model. , 2000, Cancer practice.

[36]  J. Ritchie,et al.  QUALITATIVE RESEARCH PRACTICE A GUIDE FOR SOCIAL SCIENCE STUDENTS AND RESEARCHERS , 2013 .

[37]  Kirsten Bell 'If it almost kills you that means it's working!' Cultural models of chemotherapy expressed in a cancer support group. , 2009, Social science & medicine.