Difference between revisions of "Theme:D0ad4326-4faa-47bf-85ab-a3eb78cb6540"
Marin Vidak (talk | contribs) |
|||
| Line 5: | Line 5: | ||
|Is About=This page is about participation of vulnerable groups and non-competent subjects in clinical trials. Vulnerable groups include those who could easily be influenced to participate in research, out of fear or pressure. Examples of such groups include soldiers, immigrants and prisoners.<ref>Hughes J, Hunter D, Sheehan M, Wilkinson S, Wrigley A. European textbook on ethics in research. : Publications Office of the European Union; 2010.</ref> Non-competent subjects are those who do not have the legal autonomy to make decisions for themselves, such as children and people suffering from severe mental illness or dementia. | |Is About=This page is about participation of vulnerable groups and non-competent subjects in clinical trials. Vulnerable groups include those who could easily be influenced to participate in research, out of fear or pressure. Examples of such groups include soldiers, immigrants and prisoners.<ref>Hughes J, Hunter D, Sheehan M, Wilkinson S, Wrigley A. European textbook on ethics in research. : Publications Office of the European Union; 2010.</ref> Non-competent subjects are those who do not have the legal autonomy to make decisions for themselves, such as children and people suffering from severe mental illness or dementia. | ||
<references /> | <references /> | ||
| − | |Important Because=Throughout history, scientific experiments have been conducted on human beings without their consent, especially during the World War II. As a result, specific ethical guidelines for human experimentation were developed. One of the ethical milestones in clinical research is informed consent, a process in which researchers ask for a permission before enrolling participants in a trial.<ref>Nuremberg Code (1949). The Nuremberg Code. ''Trials of war criminals before the Nuremberg military tribunals under control council law''</ref> The decision to participate has to be freely given, without pressure or conflicting interests, and based on appropriate information. Prisoners, soldiers, migrants, and other vulnerable groups are often unable to give consent in a way that satisfies the appropriate voluntary conditions. Children and patients with severe psychiatric conditions or dementia do not have the required legal capacity for granting consent. | + | |Important Because=Throughout history, scientific experiments have been conducted on human beings without their consent, especially during the World War II. As a result, specific ethical guidelines for human experimentation were developed. One of the ethical milestones in clinical research is informed consent, a process in which researchers ask for a permission before enrolling participants in a trial.<ref>Nuremberg Code (1949). The Nuremberg Code. ''Trials of war criminals before the Nuremberg military tribunals under control council law''</ref>The decision to participate has to be freely given, without pressure or conflicting interests, and based on appropriate information. Prisoners, soldiers, migrants, and other vulnerable groups are often unable to give consent in a way that satisfies the appropriate voluntary conditions. Children and patients with severe psychiatric conditions or dementia do not have the required legal capacity for granting consent. |
<references /> | <references /> | ||
|Important For=phd students; Ethics committee members; health care professionals; Researchers | |Important For=phd students; Ethics committee members; health care professionals; Researchers | ||
Latest revision as of 17:22, 25 March 2021
ThemesVulnerable and non-competent subjects in clinical trials
What is this about?
This page is about participation of vulnerable groups and non-competent subjects in clinical trials. Vulnerable groups include those who could easily be influenced to participate in research, out of fear or pressure. Examples of such groups include soldiers, immigrants and prisoners.[1] Non-competent subjects are those who do not have the legal autonomy to make decisions for themselves, such as children and people suffering from severe mental illness or dementia.
- ↑ Hughes J, Hunter D, Sheehan M, Wilkinson S, Wrigley A. European textbook on ethics in research. : Publications Office of the European Union; 2010.
Why is this important?
Throughout history, scientific experiments have been conducted on human beings without their consent, especially during the World War II. As a result, specific ethical guidelines for human experimentation were developed. One of the ethical milestones in clinical research is informed consent, a process in which researchers ask for a permission before enrolling participants in a trial.[1]The decision to participate has to be freely given, without pressure or conflicting interests, and based on appropriate information. Prisoners, soldiers, migrants, and other vulnerable groups are often unable to give consent in a way that satisfies the appropriate voluntary conditions. Children and patients with severe psychiatric conditions or dementia do not have the required legal capacity for granting consent.
- ↑ Nuremberg Code (1949). The Nuremberg Code. Trials of war criminals before the Nuremberg military tribunals under control council law
For whom is this important?
What are the best practices?
The Embassy Editorial team, Iris Lechner, Marin Vidak contributed to this theme. Latest contribution was Mar 25, 2021
