Difference between revisions of "Theme:0d054575-ca21-4209-b7c5-6120fc0ed647"
From The Embassy of Good Science
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|Theme Type=Good Practices | |Theme Type=Good Practices | ||
|Title=Informed consent | |Title=Informed consent | ||
| − | |Is About=Informed consent is a process of acquiring permission from potential participants, before conducting some sort of medical intervention, collection of personal data or enrollment in a study ( | + | |Is About=Informed consent is a process of acquiring permission from potential participants, before conducting some sort of medical intervention, collection of personal data or enrollment in a study.<ref>Cocanour CS. Informed consent-It's more than a signature on a piece of paper. Am J Surg. 2017;214(6):993-7.</ref> |
| − | |Important Because=The idea of written informed consent is not new. It first appeared in the early | + | |Important Because=In order to maintain high standards of research ethics, personal dignity and autonomy must be respected. To achieve this, before conducting research, researchers have to seek informed consent from participants. |
| + | |Important For=phd students | ||
| + | |Has Best Practice=The idea of written informed consent is not new. It first appeared in the early 20<sup>th</sup> century in Walter Reed’s research of yellow fever.<ref>Cutter L. Walter Reed, Yellow Fever, and Informed Consent. Mil Med. 2016;181(1):90-1.</ref> The development of human rights after the second World War brought to life numerous declarations and rules regarding human experimentation.<ref>Merz JF. The Nuremberg Code and Informed Consent for Research: JAMA. 2018 Jan 2;319(1):85-86. doi: 10.1001/jama.2017.17704.</ref> One of the basic concepts in human research ethics is informed consent. In order for informed consent to be valid, researchers have to provide enough information so that participant can make an informed decision. Such information has to be provided in a way that it can be understood by participants with different educational abilities. This process is called disclosure. In order to make sure that they have the ability to understand what the research is about and the ability to make a reasonable decision, a researcher must assess the mental capacity of the participant. In the end, the researcher has to be sure that the participant makes a decision freely, without pressure or manipulation (voluntariness). <ref>Miracle VA. The Belmont Report: The Triple Crown of Research Ethics. Dimens Crit Care Nurs. 2016;35(4):223-8.</ref> | ||
| − | Before accepting a manuscript for publication, editors should make sure authors have all the necessary | + | Before accepting a manuscript for publication, editors should make sure authors have all the necessary research ethics permissions and signed informed consent forms from all participants. |
| − | |||
|Has Reference=a | |Has Reference=a | ||
}} | }} | ||
| − | {{Related To}} | + | {{Related To |
| + | |Related To Theme=Theme:F72dcd0f-c164-4604-83c1-17cbf52ca717 | ||
| + | }} | ||
{{Tags | {{Tags | ||
| − | |Has Good Practice And Misconduct= | + | |Involves=Katie Gillies |
| + | |Has Virtue And Value=Respect | ||
| + | |Has Good Practice And Misconduct=Informed consent; Vulnerable and non-competent subjects | ||
}} | }} | ||
Revision as of 15:58, 10 February 2020
ThemesInformed consent
What is this about?
Informed consent is a process of acquiring permission from potential participants, before conducting some sort of medical intervention, collection of personal data or enrollment in a study.[1]
Why is this important?
In order to maintain high standards of research ethics, personal dignity and autonomy must be respected. To achieve this, before conducting research, researchers have to seek informed consent from participants.
For whom is this important?
What are the best practices?
The idea of written informed consent is not new. It first appeared in the early 20th century in Walter Reed’s research of yellow fever.[2] The development of human rights after the second World War brought to life numerous declarations and rules regarding human experimentation.[3] One of the basic concepts in human research ethics is informed consent. In order for informed consent to be valid, researchers have to provide enough information so that participant can make an informed decision. Such information has to be provided in a way that it can be understood by participants with different educational abilities. This process is called disclosure. In order to make sure that they have the ability to understand what the research is about and the ability to make a reasonable decision, a researcher must assess the mental capacity of the participant. In the end, the researcher has to be sure that the participant makes a decision freely, without pressure or manipulation (voluntariness). [4]
Before accepting a manuscript for publication, editors should make sure authors have all the necessary research ethics permissions and signed informed consent forms from all participants.The Embassy Editorial team, Iris Lechner, Mohammad Hosseini, Ružica Tokalić contributed to this theme. Latest contribution was Mar 25, 2021
Other information
Who
Virtues & Values
Good Practices & Misconduct
- ↑ Cocanour CS. Informed consent-It's more than a signature on a piece of paper. Am J Surg. 2017;214(6):993-7.
- ↑ Cutter L. Walter Reed, Yellow Fever, and Informed Consent. Mil Med. 2016;181(1):90-1.
- ↑ Merz JF. The Nuremberg Code and Informed Consent for Research: JAMA. 2018 Jan 2;319(1):85-86. doi: 10.1001/jama.2017.17704.
- ↑ Miracle VA. The Belmont Report: The Triple Crown of Research Ethics. Dimens Crit Care Nurs. 2016;35(4):223-8.
