| scholarly article | Q13442814 |
| P2093 | author name string | Deborah L Volker | |
| Hung-Lan Wu | |||
| P2860 | cites work | Self-efficacy: toward a unifying theory of behavioral change | Q28267991 |
| An attributional theory of achievement motivation and emotion | Q30052055 | ||
| How would terminally ill patients have others make decisions for them in the event of decisional incapacity? A longitudinal study | Q33306751 | ||
| Exploring cancer treatment decision-making by patients: a descriptive study | Q34035505 | ||
| Problem-solving style and adaptation in breast cancer survivors: a prospective analysis | Q34168394 | ||
| Development of the Multidimensional Health Locus of Control (MHLC) Scales | Q34273136 | ||
| Preferred roles in treatment decision making among patients with cancer: a pooled analysis of studies using the Control Preferences Scale. | Q34485529 | ||
| Control and end-of-life care: does ethnicity matter? | Q34606753 | ||
| Generalized expectancies for internal versus external control of reinforcement | Q34702911 | ||
| The influence of spiritual beliefs and practices on the treatment preferences of African Americans: a review of the literature | Q36091826 | ||
| Information giving and decision-making in patients with advanced cancer: a systematic review. | Q36142808 | ||
| Are regional variations in end-of-life care intensity explained by patient preferences?: A Study of the US Medicare Population | Q36286072 | ||
| Do religious/spiritual coping strategies affect illness adjustment in patients with cancer? A systematic review of the literature | Q36373918 | ||
| The state of advance care planning: one decade after SUPPORT. | Q36632752 | ||
| A review of barriers to utilization of the medicare hospice benefits in urban populations and strategies for enhanced access | Q36725019 | ||
| Proxy perspectives regarding end-of-life care for persons with cancer. | Q36802836 | ||
| Using the experiences of bereaved caregivers to inform patient- and caregiver-centered advance care planning | Q36870380 | ||
| Where people die: a multilevel approach to understanding influences on site of death in America | Q36904099 | ||
| What explains racial differences in the use of advance directives and attitudes toward hospice care? | Q37074123 | ||
| Racial and ethnic differences in advance care planning among patients with cancer: impact of terminal illness acknowledgment, religiousness, and treatment preferences | Q37125074 | ||
| Where the dying live: a systematic review of determinants of place of end-of-life cancer care | Q37366190 | ||
| Place of death of Houston area residents with cancer over a two-year period | Q39654348 | ||
| How do cancer patients who try to take control of their disease differ from those who do not? | Q39687401 | ||
| Patient control and end-of-life care part II: the advanced practice nurse perspective | Q39695244 | ||
| Rural and urban breast cancer patients: health locus of control and psychological adjustment | Q39826809 | ||
| Future of cancer incidence in the United States: burdens upon an aging, changing nation | Q39983611 | ||
| Timing of referral to hospice and quality of care: length of stay and bereaved family members' perceptions of the timing of hospice referral | Q40201718 | ||
| Confronting death: perceptions of a good death in adults with lung cancer | Q42640930 | ||
| Quality of life of cancer patients receiving inpatient and home-based palliative care | Q43842922 | ||
| Perceived control and psychological distress in women with breast cancer: a longitudinal study | Q44015186 | ||
| Planning for end-of-life care: findings from the Canadian Study of Health and Aging. | Q45779976 | ||
| End-of-life care in black and white: race matters for medical care of dying patients and their families. | Q46847732 | ||
| The moderating effects of anxiety and breast cancer locus of control on depression | Q47261897 | ||
| Good and bad death: introduction | Q47359526 | ||
| Exploring perceptions of cancer care delivery among older Mexican American adults | Q47583758 | ||
| Personal control over the cure of breast cancer: adaptiveness, underlying beliefs and correlates. | Q47585996 | ||
| When death is imminent: where terminally ill patients with cancer prefer to die and why. | Q47795183 | ||
| Making sense of living under the shadow of death: adjusting to a recurrent breast cancer illness | Q49111429 | ||
| Factors associated with home versus institutional death among cancer patients in Connecticut | Q49214704 | ||
| Cognitive adaptation theory and breast cancer recurrence: Are there limits? | Q50922354 | ||
| Experienced personal control and quality of life in late-stage cancer patients. | Q51250339 | ||
| A structural model of the relationships between perceived control and adaptation to illness in women with breast cancer. | Q51905907 | ||
| Will it hurt less if i can control it? A complex answer to a simple question | Q52293118 | ||
| Patient control and end-of-life care part I: the advanced practice nurse perspective. | Q53327355 | ||
| Family discord and proxy decision makers' end-of-life treatment decisions. | Q53525088 | ||
| Preferences of advanced lung cancer patients for patient-centred information and decision-making: A prospective multicentre study in 13 hospitals in Belgium | Q58128247 | ||
| The adaptive role of perceived control before and after cancer diagnosis: A prospective study | Q59453465 | ||
| Information needs and decisional preferences in women with breast cancer | Q73328389 | ||
| Access to hospice care. Expanding boundaries, overcoming barriers | Q73426942 | ||
| Persistence of racial disparities in advance care plan documents among nursing home residents | Q74167742 | ||
| Factors associated with site of death: a national study of where people die | Q78851097 | ||
| Coping with ovarian cancer risk: the moderating effects of perceived control on coping and adjustment | Q79219373 | ||
| Information needs and decision-making preferences: comparing findings for gynaecological, breast and colorectal cancer | Q80553515 | ||
| Beyond polarization, public preferences suggest policy opportunities to address aging, dying, and family caregiving | Q83172666 | ||
| A new era of for-profit hospice care--the Medicare benefit | Q84123025 | ||
| P433 | issue | 12 | |
| P304 | page(s) | 1618-1631 | |
| P577 | publication date | 2011-07-06 | |
| P1433 | published in | Qualitative Health Research | Q7268689 |
| P1476 | title | Cancer patients' preferences for control at the end of life | |
| P478 | volume | 21 |
| Q48231058 | A good death from the perspective of palliative cancer patients. |
| Q36210833 | Advance care planning in patients with incurable cancer: study protocol for a randomised controlled trial |
| Q52604798 | Associations between Race and Dementia Status and the Quality of End-of-Life Care. |
| Q47704300 | Bereaved carers' accounts of the end of life and the role of care providers in a 'good death': A qualitative study |
| Q48009848 | Cancer patient autonomy and quality of dying-a prospective nationwide survey in Taiwan |
| Q42685085 | Competing discourses surrounding primary caregivers of hospice patients |
| Q35667628 | Coping with physical and psychological symptoms: a qualitative study of advanced lung cancer patients and their family caregivers |
| Q33786245 | Experiences and Preferences for End-of-Life Care for Young Adults with Cancer and Their Informal Carers: A Narrative Synthesis |
| Q93049202 | Exploration of Patients' Spiritual/Religious Beliefs and Resuscitation Decisions |
| Q38566566 | Qualitative approaches to understanding patient preferences |
| Q38641198 | Theories of Health Care Decision Making at the End of Life: A Meta-Ethnography. |
| Q42648899 | Understanding psycho-social processes underpinning engagement with services in motor neurone disease: a qualitative study |
| Q47761049 | What Facilitates "Patient Empowerment" in Cancer Patients During Follow-Up: A Qualitative Systematic Review of the Literature. |
| Q26777486 | Withdrawal of anticancer therapy in advanced disease: a systematic literature review |
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