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Ruth Mccorkle

Datos Biográficos

ID1736341
NOMBRERuth Mccorkle
NOMBRESRuth
APELLIDOMccorkle
FIRMAMCCORKLE R
AFILIACIONESYale University
ORCID0000-0001-6578-5441
VERIFICADOSí
TOTAL DE OBRAS19
TOTAL DE CITAS28
TOTAL COMO AUTOR17
TOTAL COMO EDITOR2
PRIMER AÑO DE PUBLICACIÓN1983
AÑO MÁS RECIENTE DE PUBLICACIÓN2016
ÍNDICE H4
  • Exploring the individual patterns of spiritual well-being in people newly diagnosed with advanced cancer

    Open Access•Mei Bai, Huijie Du et al.•ARTICLE•Quality of Life Research•2016

  • Psycho-Oncology

    Jimmie C Holland, William S Breitbart et al.•BOOK•Psycho-Oncology•2015

    Originally published by Oxford in 1998, Psycho-Oncology was the first comprehensive text in the field and remains the gold standard today. Edited by a team of leading experts in psycho-oncology, spearheaded by Dr. Jimmie C. Holland, the founder of the field, the text reflects the interdisciplinary nature and global reach of this growing field. Thoroughly updated and developed in collaboration with the American Psychosocial Society and the Interna…

  • Processes of Self‐Management in Chronic Illness

    Open Access•Dena Schulman‐Green, Sarah S Jaser et al.•ARTICLE•Journal of Nursing Scholarship•2012

    Purpose: Self‐management is a dynamic process in which individuals actively manage a chronic illness. Self‐management models are limited in their specification of the processes of self‐management. The purpose of this article is to delineate processes of self‐management in order to help direct interventions and improve health outcomes for individuals with a chronic illness. Design: Qualitative metasynthesis techniques were used to analyze 101 stud…

  • Cancer Caregiving in the United States

    Open Access•Ronda C Talley, Ruth Mccorkle et al.•BOOK•Cancer Caregiving in the United…•2012

  • Caring for Grieving Family Members

    Colleen L Barry, Melissa Carlson et al.•ARTICLE•Medical Care•2012•Referencias: 20

    BACKGROUND: A founding principle of hospice is that the patient and family is the unit of care; however, we lack national information on services to family members. Although Medicare certification requires bereavement services be provided, reimbursement rates are not tied to the level or quality of care; therefore, limited financial incentives exist for hospice to provide more than a minimal benefit. OBJECTIVES: To assess the scope and intensity …

  • Quality of life among testicular cancer survivors

    Open Access•Christopher Kim, Katherine A McGlynn et al.•ARTICLE•Quality of Life Research•2011

  • Quality of Palliative Care at US Hospices

    Melissa Carlson, Melissa D A Carlson et al.•ARTICLE•Medical Care•2011

    BACKGROUND: The National Quality Forum (NQF) identified hospice services as a national priority area for health care quality improvement and endorsed a set of preferred practices for quality palliative and hospice care. This study reports the first national data regarding hospices' self-reported implementation of the NQF preferred practices and identifies hospice characteristics associated with more comprehensive implementation. METHODS: We condu…

  • The Florence Schorske Wald Professor of Nursing Endowed Chair

    Open Access•Ruth Mccorkle•ARTICLE•Illness Crisis & Loss•2009•Referencias: 8

    Setting the purpose and honor of an endowed chair in context, this article explains the great privilege that encompasses the author's holding of the Florence Schorske Wald Endowed Chair in Nursing. Wald served as a professional inspiration through her foundational work in end-of-life care and hospice institutions, the fruits of which can be seen in Dr. McCorkle's own pursuit of more dignified institutional care for the dying. Throughout Dr. McCor…

  • Reply to Commentary by Dr Peterson and Dr Groenvold

    Open Access•Siew Tzuh Tang, Ruth Mccorkle•ARTICLE•Quality of Life Research•2006

  • Comparison of health-related quality of life questionnaires in ambulatory oncology

    Open Access•Mary E Cooley, Ruth Mccorkle et al.•ARTICLE•Quality of Life Research•2005

  • Factors Related to Depressive Symptoms Among Long-Term Survivors of Cervical Cancer

    Ruth Mccorkle, Siew Tzuh Tang et al.•ARTICLE•Health Care For Women International•2005

    In this article we describe depressive symptoms among survivors of cervical cancer. Study participants were previously diagnosed and treated with cervical cancer 5 to 25 years prior to the completion of a telephone survey. Through a population-based survey of women identified via a state tumor registry in southern New England, the investigators learned that depressive symptoms are prevalent among a subgroup of long-term survivors long after diagn…

  • Discrepancy in the preferences of place of death between terminally ill cancer patients and their primary family caregivers in Taiwan

    Open Access•Siew Tzuh Tang, Tsang-Wu Liu et al.•ARTICLE•Social Science & Medicine•2005•Citada por: 4•Referencias: 32

  • Appropriate time frames for data collection in quality of life research among cancer patients at the end of life

    Open Access•Siew Tzuh Tang, Ruth Mccorkle•ARTICLE•Quality of Life Research•2002

  • Palliative care for HIV disease in the era of highly active antiretroviral therapy

    Open Access•Barbara Greenberg, Ruth Mccorkle et al.•ARTICLE•Journal of Urban Health•2000

  • Social factors, treatment, and survival in early-stage non-small cell lung cancer

    H P Greenwald, Nayak L Polissar et al.•ARTICLE•American Journal of Public Health•1998•Citada por: 10•Referencias: 19

    OBJECTIVES: This study assessed the importance of socioeconomic status, race, and likelihood of receiving surgery in explaining mortality among patients with stage-I non-small cell lung cancer. METHODS: Analyses focused on Black and White individuals 75 years of age and younger (n = 5189) diagnosed between 1980 and 1982 with stage-I non-small cell lung cancer in Detroit, San Francisco, and Seattle. The main outcome measure was months of survival …

  • Psychological distress in survivors of residential fires

    Open Access•Anne Keane, Mary Pickett et al.•ARTICLE•Social Science & Medicine•1994•Citada por: 2•Referencias: 8

  • Work disability among cancer patients

    Open Access•H P Greenwald, Susan J Dirk et al.•ARTICLE•Social Science & Medicine•1989•Citada por: 4•Referencias: 18

  • Distress, Dependency, and Threat in Newly Diagnosed Cancer and Heart Disease Patients

    Gary Donaldson, Ruth Mccorkle et al.•ARTICLE•Multivariate Behavioral Research•1986

    The effects of life-threatening illness on 56 lung cancer and 65 heart attack patients at one and two months postdiagnosis were assessed with objective self-report inventories measuring symptom distress, social dependency, concerns, mood, personality, and evaluation of problem management. Lung cancer patients had more symptom distress and concerns, and evaluated themselves more harshly, than heart attack patients. Although symptom distress remain…

  • Symptom distress, current concerns and mood disturbance after diagnosis of life-threatening disease

    Open Access•Ruth Mccorkle, Jeanne Quint-Benoliel•ARTICLE•Social Science & Medicine•1983•Citada por: 8•Referencias: 2

  • Social factors, treatment, and survival in early-stage non-small cell lung cancer

    H P Greenwald, Nayak L Polissar et al.•ARTICLE•American Journal of Public Health•1998•Citada por: 10•Referencias: 19

    OBJECTIVES: This study assessed the importance of socioeconomic status, race, and likelihood of receiving surgery in explaining mortality among patients with stage-I non-small cell lung cancer. METHODS: Analyses focused on Black and White individuals 75 years of age and younger (n = 5189) diagnosed between 1980 and 1982 with stage-I non-small cell lung cancer in Detroit, San Francisco, and Seattle. The main outcome measure was months of survival …

  • Symptom distress, current concerns and mood disturbance after diagnosis of life-threatening disease

    Open Access•Ruth Mccorkle, Jeanne Quint-Benoliel•ARTICLE•Social Science & Medicine•1983•Citada por: 8•Referencias: 2

  • Discrepancy in the preferences of place of death between terminally ill cancer patients and their primary family caregivers in Taiwan

    Open Access•Siew Tzuh Tang, Tsang-Wu Liu et al.•ARTICLE•Social Science & Medicine•2005•Citada por: 4•Referencias: 32

  • Work disability among cancer patients

    Open Access•H P Greenwald, Susan J Dirk et al.•ARTICLE•Social Science & Medicine•1989•Citada por: 4•Referencias: 18

  • Psychological distress in survivors of residential fires

    Open Access•Anne Keane, Mary Pickett et al.•ARTICLE•Social Science & Medicine•1994•Citada por: 2•Referencias: 8

  • Symptom distress, current concerns and mood disturbance after diagnosis of life-threatening disease

    Open Access•Ruth Mccorkle, Jeanne Quint-Benoliel•ARTICLE•Social Science & Medicine•1983•Citada por: 8•Referencias: 2

  • Distress, Dependency, and Threat in Newly Diagnosed Cancer and Heart Disease Patients

    Gary Donaldson, Ruth Mccorkle et al.•ARTICLE•Multivariate Behavioral Research•1986

    The effects of life-threatening illness on 56 lung cancer and 65 heart attack patients at one and two months postdiagnosis were assessed with objective self-report inventories measuring symptom distress, social dependency, concerns, mood, personality, and evaluation of problem management. Lung cancer patients had more symptom distress and concerns, and evaluated themselves more harshly, than heart attack patients. Although symptom distress remain…

  • Work disability among cancer patients

    Open Access•H P Greenwald, Susan J Dirk et al.•ARTICLE•Social Science & Medicine•1989•Citada por: 4•Referencias: 18

  • Psychological distress in survivors of residential fires

    Open Access•Anne Keane, Mary Pickett et al.•ARTICLE•Social Science & Medicine•1994•Citada por: 2•Referencias: 8

  • Social factors, treatment, and survival in early-stage non-small cell lung cancer

    H P Greenwald, Nayak L Polissar et al.•ARTICLE•American Journal of Public Health•1998•Citada por: 10•Referencias: 19

    OBJECTIVES: This study assessed the importance of socioeconomic status, race, and likelihood of receiving surgery in explaining mortality among patients with stage-I non-small cell lung cancer. METHODS: Analyses focused on Black and White individuals 75 years of age and younger (n = 5189) diagnosed between 1980 and 1982 with stage-I non-small cell lung cancer in Detroit, San Francisco, and Seattle. The main outcome measure was months of survival …

  • Palliative care for HIV disease in the era of highly active antiretroviral therapy

    Open Access•Barbara Greenberg, Ruth Mccorkle et al.•ARTICLE•Journal of Urban Health•2000

  • Appropriate time frames for data collection in quality of life research among cancer patients at the end of life

    Open Access•Siew Tzuh Tang, Ruth Mccorkle•ARTICLE•Quality of Life Research•2002

  • Comparison of health-related quality of life questionnaires in ambulatory oncology

    Open Access•Mary E Cooley, Ruth Mccorkle et al.•ARTICLE•Quality of Life Research•2005

  • Factors Related to Depressive Symptoms Among Long-Term Survivors of Cervical Cancer

    Ruth Mccorkle, Siew Tzuh Tang et al.•ARTICLE•Health Care For Women International•2005

    In this article we describe depressive symptoms among survivors of cervical cancer. Study participants were previously diagnosed and treated with cervical cancer 5 to 25 years prior to the completion of a telephone survey. Through a population-based survey of women identified via a state tumor registry in southern New England, the investigators learned that depressive symptoms are prevalent among a subgroup of long-term survivors long after diagn…

  • Discrepancy in the preferences of place of death between terminally ill cancer patients and their primary family caregivers in Taiwan

    Open Access•Siew Tzuh Tang, Tsang-Wu Liu et al.•ARTICLE•Social Science & Medicine•2005•Citada por: 4•Referencias: 32

  • Reply to Commentary by Dr Peterson and Dr Groenvold

    Open Access•Siew Tzuh Tang, Ruth Mccorkle•ARTICLE•Quality of Life Research•2006

  • The Florence Schorske Wald Professor of Nursing Endowed Chair

    Open Access•Ruth Mccorkle•ARTICLE•Illness Crisis & Loss•2009•Referencias: 8

    Setting the purpose and honor of an endowed chair in context, this article explains the great privilege that encompasses the author's holding of the Florence Schorske Wald Endowed Chair in Nursing. Wald served as a professional inspiration through her foundational work in end-of-life care and hospice institutions, the fruits of which can be seen in Dr. McCorkle's own pursuit of more dignified institutional care for the dying. Throughout Dr. McCor…

  • Quality of life among testicular cancer survivors

    Open Access•Christopher Kim, Katherine A McGlynn et al.•ARTICLE•Quality of Life Research•2011

  • Quality of Palliative Care at US Hospices

    Melissa Carlson, Melissa D A Carlson et al.•ARTICLE•Medical Care•2011

    BACKGROUND: The National Quality Forum (NQF) identified hospice services as a national priority area for health care quality improvement and endorsed a set of preferred practices for quality palliative and hospice care. This study reports the first national data regarding hospices' self-reported implementation of the NQF preferred practices and identifies hospice characteristics associated with more comprehensive implementation. METHODS: We condu…

  • Processes of Self‐Management in Chronic Illness

    Open Access•Dena Schulman‐Green, Sarah S Jaser et al.•ARTICLE•Journal of Nursing Scholarship•2012

    Purpose: Self‐management is a dynamic process in which individuals actively manage a chronic illness. Self‐management models are limited in their specification of the processes of self‐management. The purpose of this article is to delineate processes of self‐management in order to help direct interventions and improve health outcomes for individuals with a chronic illness. Design: Qualitative metasynthesis techniques were used to analyze 101 stud…

  • Cancer Caregiving in the United States

    Open Access•Ronda C Talley, Ruth Mccorkle et al.•BOOK•Cancer Caregiving in the United…•2012

  • Caring for Grieving Family Members

    Colleen L Barry, Melissa Carlson et al.•ARTICLE•Medical Care•2012•Referencias: 20

    BACKGROUND: A founding principle of hospice is that the patient and family is the unit of care; however, we lack national information on services to family members. Although Medicare certification requires bereavement services be provided, reimbursement rates are not tied to the level or quality of care; therefore, limited financial incentives exist for hospice to provide more than a minimal benefit. OBJECTIVES: To assess the scope and intensity …

  • Psycho-Oncology

    Jimmie C Holland, William S Breitbart et al.•BOOK•Psycho-Oncology•2015

    Originally published by Oxford in 1998, Psycho-Oncology was the first comprehensive text in the field and remains the gold standard today. Edited by a team of leading experts in psycho-oncology, spearheaded by Dr. Jimmie C. Holland, the founder of the field, the text reflects the interdisciplinary nature and global reach of this growing field. Thoroughly updated and developed in collaboration with the American Psychosocial Society and the Interna…

  • Exploring the individual patterns of spiritual well-being in people newly diagnosed with advanced cancer

    Open Access•Mei Bai, Huijie Du et al.•ARTICLE•Quality of Life Research•2016

Medicine (19 obras) · Internal Medicine (11 obras) · Nursing (10 obras) · Palliative Care and End-of-Life Issues (10 obras) · Psychology (10 obras) · Gerontology (9 obras) · Cancer (8 obras) · Cancer survivorship and care (5 obras) · Demography (4 obras) · Disease (4 obras)

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