Lista de obras - Susan E. McClement - Dominio Público Uruguay

"Caring as if it were my family": health care aides' perspectives about expert care of the dying resident in a personal care home

artículo científico publicado en 2009

A Qualitative Analysis of "Naturalistic" Conversations in a Peer-Led Online Support Community for Lung Cancer

artículo científico publicado en 2014

A comparison of patient and family caregiver prospective control over lung cancer ⬇️

artículo científico publicado el 25 de agosto de 2011

A dyadic affair: who is to blame for causing and controlling the patient's lung cancer?

artículo científico publicado en 2008

Acquiring an evidence base in palliative care: challenges and future directions

artículo científico publicado en 2006

An exploration of the patient navigator role: perspectives of younger women with breast cancer

artículo científico

Asking the right question of informal caregivers about patient symptom experiences: multiple proxy perspectives and reducing interrater gap.

artículo científico publicado en 2007

Assessing Symptoms, Concerns, and Quality of Life in Noncancer Patients at End of Life: How Concordant Are Patients and Family Proxy Members?

artículo científico publicado en 2018

Audio-taping the oncology treatment consultation: a literature review.

artículo científico publicado en 1999

Burden to others and the terminally ill.

artículo científico publicado en 2007

Caregiver Thoughts and Feelings in Response to Different Perspective-Taking Prompts

article

Clarifying the information and support needs of family caregivers of nursing home residents with advancing dementia

artículo científico publicado en 2020

Client and Responder Perceptions of a Personal Emergency Response System: Lifeline

article

Compassion in Health Care: An Empirical Model

artículo científico publicado en 2015

Defining dignity in terminally ill cancer patients: a factor-analytic approach

artículo científico publicado en 2004

Development and validation of a patient-reported measure of compassion in healthcare: the Sinclair Compassion Questionnaire (SCQ)

artículo científico publicado en 2021

Dignity in the Terminally Ill: Revisited

Dignity in the terminally ill: a cross-sectional, cohort study

artículo científico publicado en 2002

Dignity in the terminally ill: a developing empirical model

artículo científico publicado en 2002

Dignity therapy: a feasibility study of elders in long-term care

artículo científico publicado en 2012

Dignity therapy: a novel psychotherapeutic intervention for patients near the end of life

artículo científico publicado en 2005

Dignity therapy: family member perspectives

artículo científico publicado en 2007

Does access to a colorectal cancer screening website and/or a nurse-managed telephone help line provided to patients by their family physician increase fecal occult blood test uptake?: A pragmatic cluster randomized controlled trial study protocol

artículo científico publicado en 2012

Does access to a colorectal cancer screening website and/or a nurse-managed telephone help line provided to patients by their family physician increase fecal occult blood test uptake?: results from a pragmatic cluster randomized controlled trial

artículo científico publicado en 2014

Does blaming the patient with lung cancer affect the helping behavior of primary caregivers?

artículo científico publicado en 2008

Effect of dignity therapy on distress and end-of-life experience in terminally ill patients: a randomised controlled trial

artículo científico publicado en 2011

Eliciting Personhood Within Clinical Practice: Effects on Patients, Families, and Health Care Providers

artículo científico publicado en 2014

Expert nursing behaviors in care of the dying adult in the intensive care unit

artículo científico publicado en 1995

Family beliefs regarding the nutritional care of a terminally ill relative: a qualitative study

artículo científico publicado en 2003

Family members' experiences caring for patients with advanced head and neck cancer receiving tube feeding: a descriptive phenomenological study.

artículo científico publicado en 2012

Family presence during resuscitation: Canadian critical care nurses' perspectives

artículo científico publicado en 2009

Family satisfaction with care of a dying loved one in nursing homes: what makes the difference?

artículo científico publicado en 2008

Fecal occult blood testing instructions and impact on patient adherence

artículo científico publicado en 2012

Health care provider communication: an empirical model of therapeutic effectiveness

artículo científico publicado en 2013

Impact of patient smoking behavior on empathic helping by family caregivers in lung cancer.

artículo científico publicado en 2012

Learning from dying patients during their final days: life reflections gleaned from dignity therapy

artículo científico publicado en 2010

Nurses' perceptions of quality end-of-life care on an acute medical ward

artículo científico publicado en 2006

Nurses' responses to initial moral distress in long-term care

artículo científico publicado en 2013

Parental Experiences of Adult Child Death from Cancer

article

Personality, neuroticism, and coping towards the end of life

artículo científico publicado en 2006

Pilot study of a survey to identify the prevalence of and risk factors for chronic neuropathic pain following breast cancer surgery

artículo científico publicado en 2012

Spousal bereavement: the lived experience of young Canadian widows

artículo científico publicado en 2010

Symptom distress in adult patients with cancer

artículo científico publicado en 1997

The TIME Questionnaire: A tool for eliciting personhood and enhancing dignity in nursing homes

artículo científico publicado en 2016

The landscape of distress in the terminally ill.

artículo científico publicado en 2009

The patient dignity inventory: a novel way of measuring dignity-related distress in palliative care

Understanding bereaved family members' dissatisfaction with end-of-life care in nursing homes

artículo científico publicado en 2012

Understanding the will to live in patients nearing death

artículo científico publicado en 2005

What is the role of family in promoting faecal occult blood test screening? Exploring physician, average-risk individual, and family perceptions

artículo científico publicado en 2012

Lista de obras de Susan E. McClement

"Caring as if it were my family": health care aides' perspectives about expert care of the dying resident in a personal care home

A Qualitative Analysis of "Naturalistic" Conversations in a Peer-Led Online Support Community for Lung Cancer

A comparison of patient and family caregiver prospective control over lung cancer ⬇️

A dyadic affair: who is to blame for causing and controlling the patient's lung cancer?

Acquiring an evidence base in palliative care: challenges and future directions

An exploration of the patient navigator role: perspectives of younger women with breast cancer

Asking the right question of informal caregivers about patient symptom experiences: multiple proxy perspectives and reducing interrater gap.

Assessing Symptoms, Concerns, and Quality of Life in Noncancer Patients at End of Life: How Concordant Are Patients and Family Proxy Members?

Audio-taping the oncology treatment consultation: a literature review.

Burden to others and the terminally ill.

Caregiver Thoughts and Feelings in Response to Different Perspective-Taking Prompts

Clarifying the information and support needs of family caregivers of nursing home residents with advancing dementia

Client and Responder Perceptions of a Personal Emergency Response System: Lifeline

Compassion in Health Care: An Empirical Model

Defining dignity in terminally ill cancer patients: a factor-analytic approach

Development and validation of a patient-reported measure of compassion in healthcare: the Sinclair Compassion Questionnaire (SCQ)

Dignity in the Terminally Ill: Revisited

Dignity in the terminally ill: a cross-sectional, cohort study

Dignity in the terminally ill: a developing empirical model

Dignity therapy: a feasibility study of elders in long-term care

Dignity therapy: a novel psychotherapeutic intervention for patients near the end of life

Dignity therapy: family member perspectives

Does access to a colorectal cancer screening website and/or a nurse-managed telephone help line provided to patients by their family physician increase fecal occult blood test uptake?: A pragmatic cluster randomized controlled trial study protocol

Does access to a colorectal cancer screening website and/or a nurse-managed telephone help line provided to patients by their family physician increase fecal occult blood test uptake?: results from a pragmatic cluster randomized controlled trial

Does blaming the patient with lung cancer affect the helping behavior of primary caregivers?

Effect of dignity therapy on distress and end-of-life experience in terminally ill patients: a randomised controlled trial

Eliciting Personhood Within Clinical Practice: Effects on Patients, Families, and Health Care Providers

Expert nursing behaviors in care of the dying adult in the intensive care unit

Family beliefs regarding the nutritional care of a terminally ill relative: a qualitative study

Family members' experiences caring for patients with advanced head and neck cancer receiving tube feeding: a descriptive phenomenological study.

Family presence during resuscitation: Canadian critical care nurses' perspectives

Family satisfaction with care of a dying loved one in nursing homes: what makes the difference?

Fecal occult blood testing instructions and impact on patient adherence

Health care provider communication: an empirical model of therapeutic effectiveness

Impact of patient smoking behavior on empathic helping by family caregivers in lung cancer.

Learning from dying patients during their final days: life reflections gleaned from dignity therapy

Nurses' perceptions of quality end-of-life care on an acute medical ward

Nurses' responses to initial moral distress in long-term care

Parental Experiences of Adult Child Death from Cancer

Personality, neuroticism, and coping towards the end of life

Pilot study of a survey to identify the prevalence of and risk factors for chronic neuropathic pain following breast cancer surgery

Spousal bereavement: the lived experience of young Canadian widows

Symptom distress in adult patients with cancer

The TIME Questionnaire: A tool for eliciting personhood and enhancing dignity in nursing homes

The landscape of distress in the terminally ill.

The patient dignity inventory: a novel way of measuring dignity-related distress in palliative care

Understanding bereaved family members' dissatisfaction with end-of-life care in nursing homes

Understanding the will to live in patients nearing death

What is the role of family in promoting faecal occult blood test screening? Exploring physician, average-risk individual, and family perceptions