Jason H T Karlawish
Biographic Data
| ID | 5541222 |
|---|---|
| NAME | Jason H T Karlawish |
| GIVEN NAMES | Jason H T |
| FAMILY NAME | Karlawish |
| SIGNATURE | KARLAWISH J H T |
| VERIFIED | No |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2002 |
| LATEST PUBLICATION YEAR | 2002 |
| H-INDEX | 0 |
A Taxonomy of Value in Clinical Research
Medical research that involves human subjects presents what appears to be an intractable ethical problem: patients are exposed to risks in order to create valuable knowledge. A central goal of research is to produce knowledge that is "important," "fruitful," or that will have "value." Indeed, federal regulations require that research risks be reasonable in proportion to potential benefits, and in proportion to the importance of the knowledge to b…
Informed Consent for Alzheimer's Disease Clinical Trials
Jason H. T. Karlawish, David Knopman, Christopher M. Clark, John C. Morris, Daniel Marson, Peter J. Whitehouse, Claudia H. Kawas, Informed Consent for Alzheimer's Disease Clinical Trials: A Survey of Clinical Investigators, IRB: Ethics & Human Research, Vol. 24, No. 5 (Sep. - Oct., 2002), pp. 1-5
How Changes in Health Care Practices, Systems, and Research Challenge the Practice of Informed Consent
Informed consent has been the central model for ethical decision making in clinical care and research. The goal of informed consent is to protect the right of a competent person to make his or her own health care decisions based on personal values and goals. But changes in health care practices, systems, and research have challenged this well-established goal. This paper examines these changes to show that decisions about care and research direct…
No prominent works on this page.
A Taxonomy of Value in Clinical Research
Medical research that involves human subjects presents what appears to be an intractable ethical problem: patients are exposed to risks in order to create valuable knowledge. A central goal of research is to produce knowledge that is "important," "fruitful," or that will have "value." Indeed, federal regulations require that research risks be reasonable in proportion to potential benefits, and in proportion to the importance of the knowledge to b…
Informed Consent for Alzheimer's Disease Clinical Trials
Jason H. T. Karlawish, David Knopman, Christopher M. Clark, John C. Morris, Daniel Marson, Peter J. Whitehouse, Claudia H. Kawas, Informed Consent for Alzheimer's Disease Clinical Trials: A Survey of Clinical Investigators, IRB: Ethics & Human Research, Vol. 24, No. 5 (Sep. - Oct., 2002), pp. 1-5
How Changes in Health Care Practices, Systems, and Research Challenge the Practice of Informed Consent
Informed consent has been the central model for ethical decision making in clinical care and research. The goal of informed consent is to protect the right of a competent person to make his or her own health care decisions based on personal values and goals. But changes in health care practices, systems, and research have challenged this well-established goal. This paper examines these changes to show that decisions about care and research direct…
Ethics in medical practice (3 works) · Alternative medicine (2 works) · Ethics in Clinical Research (2 works) · Informed consent (2 works) · Medicine (2 works) · Palliative Care and End-of-Life Issues (2 works) · Psychology (2 works) · Alzheimer's disease (1 work) · Biology (1 work) · Biomedical Ethics and Regulation (1 work)