Verified Document

Palliative Care Perceptions Of Palliative Term Paper

The study will also include a sample of 100 patients in the same settings. All participants will range in age from 40-80, and will include a random selection of male and female patients and caregivers. Design, Setting, Instruments

Patients will be provided a questionnaire to fill out that assesses their attitudes, beliefs and feelings about the care provided to them in the past, and the care they expect from their healthcare providers. Nurses will be provided a 10 question questionnaire that will include a discussion of their roles, their attitudes and beliefs about palliative care and their involvement in palliative care decision-making processes. Nurses will also be asked to describe the level of interaction they have with patients and the education they offer patients about the palliative care treatment options available to them. Questionnaires will be scored using a Likert-type 5-point scale (Carmel, Werner & Ziedenberg, 2004) with higher numbered answers suggesting a stronger agreement with statements and lower scored questions indicating disagreement with questionnaire statements. This will provide the opportunity to conduct statistical analysis of answers and provide both internal consistency and validity (Carmel, Werner & Ziedenberg, 2004).

Ethical Implications

Patient and healthcare privacy must be protected to adhere to basic ethical and moral standards one would expect when conducting a study that includes acquisition of personal information. For purposes of this study, to protect the identities of patients and nurses or other healthcare participants, each individual participating in the study will be provided a full disclosure of the study's purpose, intent and results. Patients will be asked to provide demographic and socioeconomic information, but will not be required to provide individual identifying information such as their name, address or other personal information. Nurses will be asked to provide information about their work history and experience, but will also have the ability to answer questions anonymously so their identities are protected.

Dissemination of Results

Work Plan

The researcher expects to collect all data and compile results in digital format using statistical analysis software. The information will be distributed in two reports, one revealing patient's opinions and perceptions of palliative care and one revealing and discussing nurses' perceptions of care. The researcher will then provide a synthesis of the research material gathered from the questionnaires...

The time frame for conducting this study is as follows: - 1 month to compile questionnaires - 1 month to conduct thorough review of literature on palliative care treatments from a database containing no less than 50 peer reviewed articles on the subject matter at hand - 1 month to distribute and collect survey questionnaires, with a follow up expected 1/2 way through distribution and collection of materials and 1 - month to compile and analyze results.
Budget

The budget for this study is limited. To help reduce the costs associated with conducting a study the number of participants and locations selected are limited in size. Questionnaires will be hand delivered and picked up by the researcher at each research location so as to minimize expenses associated with mailing and delivery of materials. The researcher will rely on free or minimal cost statistical analysis software to compile information collected from the study.

References

Carmel, S., Werner, P. & Ziedenberg, H. (2004). Nurses' and social workers' attitudes and beliefs about and involvement in life-sustaining treatment decisions. Health and Social Work, 29(1): 27.

Coulton, C.J. (1990). Research in patient and family decision-making regarding life sustaining and long-term care. Social Work in Health Care, 15(1): 63-78.

Csikai, E.L. (1999). The role and experience in determining social workers' attitudes toward euthanasia and assisted suicide. Social Work in Health Care, 30(1): 75-95.

DeMarrais, K. & Lapan, S.D. (2004). Foundations for research: Methods of inquiry in education and the social sciences. Mahwah: Lawrence Erlbaum Associates.

Shoefield, R.F., & Amodeo, M. (1999). Interdisciplinary teams in health care and human services settings. Health & Social Work, 24(1): 210-19.

Solomon, M.Z., O'Donnell, L., Jennings, B., Guilfoy, V., Wolf, S.M., Nolan, K.,

Jackson, R., Koch-Weser, D., & Donnelley, S. (1993). Decisions near the end of life: Professional views of life-sustaining treatments. American Journal of Public Health, 83(1): 14-23.

Werner, P. & Carmel, S. (2001). Life-sustaining treatment decisions: Health care social workers' attitudes and…

Sources used in this document:
References

Carmel, S., Werner, P. & Ziedenberg, H. (2004). Nurses' and social workers' attitudes and beliefs about and involvement in life-sustaining treatment decisions. Health and Social Work, 29(1): 27.

Coulton, C.J. (1990). Research in patient and family decision-making regarding life sustaining and long-term care. Social Work in Health Care, 15(1): 63-78.

Csikai, E.L. (1999). The role and experience in determining social workers' attitudes toward euthanasia and assisted suicide. Social Work in Health Care, 30(1): 75-95.

DeMarrais, K. & Lapan, S.D. (2004). Foundations for research: Methods of inquiry in education and the social sciences. Mahwah: Lawrence Erlbaum Associates.
Cite this Document:
Copy Bibliography Citation

Related Documents

Palliative Care and Communication User,
Words: 3534 Length: 10 Document Type: Essay

No body of evidence has developed to support these concerns, influential though they have been. It is helpful to recognize that they are not new issues, but have frequently been identified and applied to many groups and individuals. Such concerns have often been associated with traditions of 'protecting' (vulnerable) service users, issues of 'gate keeping' by service providers and paternalistic health and welfare cultures (Brownell, 2006). This is in sharp

Palliative Care
Words: 21397 Length: 70 Document Type: Ghost Writing

Hisory of Palliatve Care Palliative Care Palliative Care Methods Palliative care entails assisting patients get through pain caused by different diseases. The patient may be ailing from any diseases, be it curable or untreatable. Even patient who are sick and almost passing away will need this care. Palliative care has characteristics that differentiate it to hospice care. The key role for palliative care is to help in improving the existence of someone and

Holistic Nursing Care Plan for Terminally Ill Patient
Words: 1497 Length: 5 Document Type: Essay

Holistic Nursing Care Plan for Terminally Ill Patient The objective of this study is to create a holistic nursing care plan for a terminally ill patient. This study will explain how perceptions about quality of life and health promotion might affect care for a dying patient with a lingering illness such as cancer and discuss strategies that could be used in the situation to improve the quality of life for the

Effect of Palliative Care on the Healthcare Professional and Family...
Words: 2777 Length: 8 Document Type: Essay

Palliative Care on the Caregiver Palliative care has several positive effects on the caregiver. These can be divided into emotional, social, psychological, and physical effects. First is the positive psychological effect that the caregiver such as the nurse, personal care worker, or family member to deal with the tough job. One study found that when patients died with unrelieved suffering, as nurses, they would also endure enormous suffering on their

Model for Community Palliative Care
Words: 1740 Length: 6 Document Type: Research Paper

Community Dementia Care and the Chronic Care Model End-Stage Dementia Evaluation Proposal Health Promotion Plan for Community End-Stage Dementia Care: The Chronic Care Model Health Promotion Plan for Community End-Stage Dementia Care: The Chronic Care Model. In 2013 an estimated 5.0 million Americans over the age of 65 suffered from Alzheimer's disease (Alzheimer's Association, 2013). Although the U.S. Centers for Disease Control and Prevention (CDC) considers dementia/Alzheimer's to be the fifth leading cause of

End-Of-Life Care Provided by Nurses in Palliative
Words: 2686 Length: 8 Document Type: Essay

End-of-life care provided by nurses in palliative settings necessitates conscious awareness of several factors that contribute to the effectiveness of care. Factors that are significantly important components of nursing in end-of-life care include communication skills, advance care planning, sensitivity to contextual and cultural factors, support from the healthcare team, and continuing education. Communication skills The importance of communication skills in end-of-life care was acknowledged by Clayton et al. (2007), who developed a

Sign Up for Unlimited Study Help

Our semester plans gives you unlimited, unrestricted access to our entire library of resources —writing tools, guides, example essays, tutorials, class notes, and more.

Get Started Now