Barriers to, and Facilitators of Physical Activity in Patients Receiving Chemotherapy for Lung Cancer: An exploratory study.

Abstract:

AIM:Physical activity (PA) has a positive effect on the cardiorespiratory fitness, lung cancer symptoms, and quality of life of lung cancer patients. The aim of our study was to identify barriers to, and facilitators of PA in lung cancer patients. METHODS:We collected data from five patients diagnosed with primary, advanced non-small-cell lung cancer (NSCLC) who were receiving chemotherapy. Choosing a qualitative approach, we conducted an exploratory analysis using the thematic analysis technique to process the data. RESULTS:Seven barriers to, and facilitators of PA were identified and grouped into four categories. We found that psychological and social factors affect patients' willingness and ability to engage in PA, while physiological and environmental factors have an impact on the duration, intensity, and regularity of their PA. CONCLUSION:Our study highlighted some of the effects that the barriers to PA have on the practice of it in our patient group. Our findings may be used by professionals to design adapted PA programs.

journal_name

J Palliat Care

authors

Mas S,Quantin X,Ninot G

doi

10.1177/082585971503100204

subject

Has Abstract

pub_date

2015-01-01 00:00:00

pages

89-96

issue

2

eissn

0825-8597

issn

2369-5293

journal_volume

31

pub_type

杂志文章
  • Communication about palliative care for patients with chronic obstructive pulmonary disease.

    abstract::Chronic obstructive pulmonary disease (COPD) is a leading cause of mortality and disability worldwide. For many patients, maximal therapy for COPD produces only modest relief of disabling symptoms and these symptoms result in a significantly reduced quality of life. Despite the high morbidity and mortality, patients w...

    journal_title:Journal of palliative care

    pub_type: 杂志文章,评审

    doi:

    authors: Curtis JR,Engelberg RA,Wenrich MD,Au DH

    更新日期:2005-10-01 00:00:00

  • The survival time of terminal cancer patients: prediction based on clinical parameters and simple prognostic scores.

    abstract:AIM:By examining clinical parameters associated with survival time and analyzing patients' survival times using prognostic scores, this study aimed to provide helpful information related to the treatment of terminal cancer patients. METHODS:We retrospectively reviewed the medical records of 415 inpatients who died in ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Kim AS,Youn CH,Ko HJ,Kim HM

    更新日期:2014-04-01 00:00:00

  • Referral of terminally ill patients for hospice: frequency and correlates.

    abstract:BACKGROUND:Despite the central role of hospice in end-of-life care, little is known about the proportion of terminally ill patients referred for hospice and the physician factors associated with hospice referral. METHODS:Cross-sectional data from a self-administered survey of 231 physicians were used to estimate the p...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Bradley EH,Fried TR,Kasl SV,Cicchetti DV,Johnson-Hurzeler R,Horwitz SM

    更新日期:2000-01-01 00:00:00

  • Determinants of place of death for recipients of home-based palliative care.

    abstract:INTRODUCTION:Health system restructuring combined with the preferences of many terminally ill care recipients and their caregivers has led to an increase in home-based palliative care, yet many care recipients die within institutional settings such as hospitals. This study sought to determine the place of death and its...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Masucci L,Guerriere DN,Cheng R,Coyte PC

    更新日期:2010-01-01 00:00:00

  • Pressure ulcer prevention and treatment in hospices: a qualitative analysis.

    abstract::There has been little research into pressure ulcer prevention and treatment in hospices. In this study, interviews with hospice directors of clinical services and direct-care nurses were analyzed using qualitative methods. Several general themes were found. Both pressure ulcer prevention and treatment can be painful t...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Eisenberger A,Zeleznik J

    更新日期:2003-04-01 00:00:00

  • The Impact of Socioeconomic Status on Place of Death Among Patients Receiving Home Palliative Care in Toronto, Canada: A Retrospective Cohort Study.

    abstract:BACKGROUND:Socioeconomic disparities in home death have been noted in the literature. Home-based palliative care increases access to home death and has been suggested as a means to decrease these disparities. AIM:Our study examines the association between socioeconomic status and other demographic factors on place of ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719855020

    authors: Wales J,Kalia S,Moineddin R,Husain A

    更新日期:2020-07-01 00:00:00

  • What constitutes high-quality HIV/AIDS palliative care?

    abstract::The study assessed the components of high-quality HIV palliative care using the multidimensional model of quality assessment developed by Maxwell (4). Data collection consisted of interviews with individual subjects and focus groups. The interviews took place in three London health authorities. Seven service users and...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Armes PJ,Higginson IJ

    更新日期:1999-01-01 00:00:00

  • Would You Be Surprised if This Patient Died in the Next 12 Months? Using the Surprise Question to Increase Palliative Care Consults From the Emergency Department.

    abstract:BACKGROUND:There is a growing movement to increase palliative care consults from the emergency department (ED) to reduce healthcare costs and improve quality of life. The surprise question is a screening tool that emergency medicine physicians may be able to use towards achieving this goal. OBJECTIVE:The objectives of...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719866698

    authors: Zeng H,Eugene P,Supino M

    更新日期:2020-10-01 00:00:00

  • The role of the pharmacist in palliative care: results of a survey conducted in Australia and Canada.

    abstract::A survey was conducted to determine what pharmaceutical services are provided to palliative care sites in Australia and Canada, and the pharmacist's role on the interdisciplinary team. Questionnaires were sent to 100 selected sites in each country. Questions pertained to demographics and the level of duties performed....

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Gilbar P,Stefaniuk K

    更新日期:2002-01-01 00:00:00

  • E-Pain Reporter: A Digital Pain and Analgesic Diary for Home Hospice Care.

    abstract::Informal hospice caregivers play a key role in managing patients' pain at home, but lack of adherence to doctor-prescribed analgesic regimens and medication errors are significant barriers to truly effective pain management. A digital pain diary may improve caregiver management of pain at home; however, most digital p...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859717722466

    authors: Mayahara M,Wilbur J,O'Mahony S,Breitenstein S

    更新日期:2017-04-01 00:00:00

  • Integration of palliative care with alternative medicine in patients who have refused curative cancer therapy: a report of two cases.

    abstract::This article describes two young, potentially curable patients who chose a course of treatment that ultimately resulted in death. Their choice was in part influenced by the prospect of the disfiguring surgery that would have been required for cure. In the first patient this would have meant massive head and neck surge...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Jenkins CA,Scarfe A,Bruera E

    更新日期:1998-01-01 00:00:00

  • Initiation of chemotherapy in cancer patients with poor performance status: a population-based analysis.

    abstract:OBJECTIVE:Practice guidelines indicate that patients who have months to weeks left to live should not be offered chemotherapy. We examined factors associated with clinician-reported poor performance status as determined by the Palliative Performance Scale (PPS) and subsequent initiation of intravenous (IV) chemotherapy...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Porter J,Earle C,Atzema C,Liu Y,Howell D,Seow H,Sutradhar R,Dudgeon D,Husain A,Sussman J,Barbera L

    更新日期:2014-10-01 00:00:00

  • Living fully in the shadow of mortal time: psychosocial assets in advanced cancer.

    abstract:OBJECTIVE:This study aimed to characterize the strategies and psychosocial conditions that influence how resilient people live in the face of advanced cancer. METHODS:Grounded theory interviews and a survey of 10 resilient people with advanced cancer were collected and analyzed. FINDINGS:Personal assets - including p...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Wise M,Marchand L

    更新日期:2013-07-01 00:00:00

  • Encounters With Health-Care Providers and Advance Directive Completion by Older Adults.

    abstract:BACKGROUND:The Patient Self-Determination Act (PSDA) requires hospitals, home health agencies, nursing homes, and hospice providers to offer new patients information about advance directives. There is little evidence regarding whether encounters with these health-care providers prompt advance directive completion by pa...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718769099

    authors: Koss C

    更新日期:2018-07-01 00:00:00

  • Advanced Cancer Patients' Perceptions of Dignity: The Impact of Psychologically Distressing Symptoms and Preparatory Grief.

    abstract:PURPOSE:The present study assesses the relationship between patient dignity in advanced cancer and the following variables: psychological distress, preparatory grief, and sociodemographic and clinical characteristics. METHODS:The sample consisted of 120 patients with advanced cancer. The self-administered questionnair...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718759882

    authors: Kostopoulou S,Parpa E,Tsilika E,Katsaragakis S,Papazoglou I,Zygogianni A,Galanos A,Mystakidou K

    更新日期:2018-04-01 00:00:00

  • Staff stress, work satisfaction, and death attitudes on an oncology palliative care unit, and on a medical and radiation oncology inpatient unit.

    abstract::Professional caregivers for cancer patients are at high risk for work-related stress, but it is not clear how this relates to exposure to death and dying, and to professional satisfaction. This study compares work-related stress and staff satisfaction on an academic acute palliative care unit (PCU) with that on a medi...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Pierce B,Dougherty E,Panzarella T,Le LW,Rodin G,Zimmermann C

    更新日期:2007-04-01 00:00:00

  • Methodologic issues in palliative care psychosocial research.

    abstract::The conduct of psychosocial research with palliative care patients or staff presents a major investigative challenge. The fragility of patients and their physical or cognitive limitations severely curtail the types of studies that are possible and the research methods that can be applied. A major limitation is that ra...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Cassileth BR,Lusk EJ

    更新日期:1989-12-01 00:00:00

  • The pattern of gabapentin use in a tertiary palliative care unit.

    abstract:BACKGROUND:Little is known about current practice in using the anticonvulsant gabapentin in the management of cancer-related neuropathic pain. OBJECTIVES:The main objective of this study was to describe the pattern of gabapentin use as an adjuvant analgesic for cancer-related neuropathic pain in patients admitted to a...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Oneschuk D,al-Shahri MZ

    更新日期:2003-10-01 00:00:00

  • Inpatient narcotic infusions for patients with cancer pain.

    abstract::Morphine and hydromorphone infusions of 6 or more (average 25.75) days in duration were used with increasing frequency (up to 7%) by our oncology inpatients. Eighty-six percent of the 135 inpatients we reviewed realized good pain control with dose rates up to 700 morphine-equivalent (ME) mg/h. Local toxicity occurred ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Ferris FD,Kerr IG,De Angelis C,Sone M,Hume S

    更新日期:1990-07-01 00:00:00

  • Volunteers in palliative care make a difference.

    abstract::Family care giving is important for the quality of life of terminally ill patients and their family members. Although family caregivers are generally eager to provide palliative care, at some point it may become too demanding, and then volunteers can make a difference. This four-study paper presents the experiences of...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Luijkx KG,Schols JM

    更新日期:2009-04-01 00:00:00

  • What Is Good Advance Care Planning According to Hospitalized Palliative Patients and Their Families? An Explorative Study.

    abstract:BACKGROUND:Advance care planning is not well implemented in Belgian hospital practice. In order to obtain successful implementation, implementation theory states that the adopters should be involved in the implementation process. This information can serve as a basis for creating better implementation strategies. AIM:...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859720938583

    authors: Vanderhaeghen B,Bossuyt I,Menten J,Rober P

    更新日期:2020-10-01 00:00:00

  • Caregiver bereavement outcome: relationship with hospice at home, satisfaction with care, and home death.

    abstract::This study used a randomized controlled trial design to investigate the impact of hospice at home (HAH) on caregiver bereavement outcome. Secondary analyses considered the association between bereavement, place of death, and carers' assessment of support. Ninety-six informal carers of patients referred to HAH were sur...

    journal_title:Journal of palliative care

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:

    authors: Grande GE,Farquhar MC,Barclay SI,Todd CJ

    更新日期:2004-07-01 00:00:00

  • Bad news for the patient and the family? The worst part of being a health care professional.

    abstract::In Spain, there is a general tendency to conceal the prognosis from a terminally ill patient. We conducted grounded-theory-based, phenomenological, qualitative research on this using a final sample of 42 in-depth interviews with doctors and nurses from different fields. We found that most health professionals believe ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Schmidt Rio-Valle J,García Caro MP,Montoya Juarez R,Prados Peña D,Muñoz Vinuesa A,Pappous A,Cruz Quintana F

    更新日期:2009-10-01 00:00:00

  • The impact on families of respite care in a children's hospice program.

    abstract::With increasing trends towards home care of children with even the most complex conditions and care requirements, respite becomes critical in improving the quality of life for terminally ill children and their families. This article reports on the respite component of an evaluation project that examined the effect of ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Davies B,Steele R,Collins JB,Cook K,Smith S

    更新日期:2004-01-01 00:00:00

  • Addressing myths about end-of-life care: research into the use of acute care hospitals over the last five years of life.

    abstract::Despite very little confirming evidence, one of the most pervasive beliefs about dying is that terminally ill people receive a great deal of health care in the last few days, weeks, or months of life. A secondary analysis of 1992/93 through 1996/97 Alberta inpatient hospital abstracts data was undertaken to explore an...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Wilson DM,Truman CD

    更新日期:2002-04-01 00:00:00

  • What is symptom burden: a qualitative exploration of patient definitions.

    abstract::Current definitions of "symptom burden" are largely derived from clinicians, and there are many variations in the way the term is used, defined, and operationalized. The aim of this study was to explore patient perceptions of symptom burden in the context of advanced and incurable disease. A group of 58 cancer patient...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Gill A,Chakraborty A,Selby D

    更新日期:2012-07-01 00:00:00

  • Longer Duration of Palliative Care in Patients With COPD Is Associated With Death Outside the Hospital.

    abstract:BACKGROUND:Patients with advanced chronic obstructive pulmonary disease (COPD) have a significant symptom burden despite maximal medical therapy, yet few are referred for concomitant palliative care. OBJECTIVE:To evaluate the utilization and impact of palliative care on the location of death and to identify clinical v...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719851486

    authors: Kraskovsky V,Schneider J,Mador MJ,Provost KA

    更新日期:2019-07-02 00:00:00

  • Paramedics' perceptions of their role in palliative care: analysis of focus group transcripts.

    abstract::Paramedics play an important role in out-of-hospital health care. They provide unscheduled care, assisting both patients with minor injuries and those experiencing life-threatening emergencies. Increasingly, paramedics are called on to manage chronic and complex health needs, including symptom relief for patients at t...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Lord B,Récoché K,O'Connor M,Yates P,Service M

    更新日期:2012-04-01 00:00:00

  • Pediatric palliative care education for medical students: development and evaluation of a pilot program.

    abstract:UNLABELLED:In Poland, medical curricula cover palliative care for adults, not for children. This paper evaluates feedback of students who participated in a pilot pediatric palliative care education program. METHOD:An anonymous questionnaire was designed for the students; they were asked to assess each aspect of the pr...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Korzeniewska-Eksterowicz A,Kedzierska B,Cynker-McCarthy M,Przysło Ł,Stolarska M,Nowicki GF,Młynarski W

    更新日期:2012-01-01 00:00:00

  • Primary care providers' perceptions of care.

    abstract::The Regional Palliative Care Unit in Ottawa conducted a retrospective study to determine how satisfied patients and families were with the service the Unit offers. Forty-five primary care providers, bereaved from 6 to 12 months, completed the 64-item semistructured telephone interview in a mean time of 20 minutes. The...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Keizer MC,Kozak JF,Scott JF

    更新日期:1992-01-01 00:00:00