Difference between revisions of "Theme:F72dcd0f-c164-4604-83c1-17cbf52ca717"

From The Embassy of Good Science
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|Title=Informed assent
 
|Title=Informed assent
 
|Is About=Informed assent is a process through which minors agree to participate in clinical trials. This is different from informed consent, because minors cannot provide consent in the full meaning of the word, as they don’t meet the legal age requirements. For minors, consent is provided by parents or legal guardians, and this process of acquiring both consent and assent is called a dual consent procedure <ref>Hein IM, De Vries MC, Troost PW, Meynen G, Van Goudoever JB, Lindauer RJ. Informed consent instead of assent is appropriate in children from the age of twelve: Policy implications of new findings on children's competence to consent to clinical research. BMC Med Ethics. 2015;16(1):015-0067.</ref>.
 
|Is About=Informed assent is a process through which minors agree to participate in clinical trials. This is different from informed consent, because minors cannot provide consent in the full meaning of the word, as they don’t meet the legal age requirements. For minors, consent is provided by parents or legal guardians, and this process of acquiring both consent and assent is called a dual consent procedure <ref>Hein IM, De Vries MC, Troost PW, Meynen G, Van Goudoever JB, Lindauer RJ. Informed consent instead of assent is appropriate in children from the age of twelve: Policy implications of new findings on children's competence to consent to clinical research. BMC Med Ethics. 2015;16(1):015-0067.</ref>.
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<references />
 
|Important Because=In order to conduct clinical research in an ethical manner, informed assent from children and informed consent from their legal guardians must be sought. Respecting both children’s wishes and asking parents’ permission is necessary in order to respect laws and rules of good clinical practice, and to respect patients’ autonomy, despite the fact that the patient is a minor <ref>Poston RD. Assent Described: Exploring Perspectives From the Inside. J Pediatr Nurs. 2016;31(6):e353-e65.</ref>.
 
|Important Because=In order to conduct clinical research in an ethical manner, informed assent from children and informed consent from their legal guardians must be sought. Respecting both children’s wishes and asking parents’ permission is necessary in order to respect laws and rules of good clinical practice, and to respect patients’ autonomy, despite the fact that the patient is a minor <ref>Poston RD. Assent Described: Exploring Perspectives From the Inside. J Pediatr Nurs. 2016;31(6):e353-e65.</ref>.
|Important For=phd students
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|Important For=Junior researchers; Senior researchers; Supervisors; PhD students; Graduate students; Early career researchers
 
|Has Reference=a
 
|Has Reference=a
 
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{{Related To
 
{{Related To
|Related To Resource=Resource:F7ed25ad-cfab-4040-b52f-596accc3c317
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|Related To Resource=Resource:F7ed25ad-cfab-4040-b52f-596accc3c317;Resource:E9cd7ee1-bd54-4d5c-bdd9-786ef1c9f603
 
|Related To Theme=Theme:0d054575-ca21-4209-b7c5-6120fc0ed647;Theme:E5629f68-81f6-490d-84d6-fd1e63b8dbc7;Theme:D0ad4326-4faa-47bf-85ab-a3eb78cb6540
 
|Related To Theme=Theme:0d054575-ca21-4209-b7c5-6120fc0ed647;Theme:E5629f68-81f6-490d-84d6-fd1e63b8dbc7;Theme:D0ad4326-4faa-47bf-85ab-a3eb78cb6540
 
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{{Tags
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|Has Virtue And Value=Honesty
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|Has Good Practice And Misconduct=Informed consent
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}}

Revision as of 12:29, 27 May 2020

Informed assent

What is this about?

Informed assent is a process through which minors agree to participate in clinical trials. This is different from informed consent, because minors cannot provide consent in the full meaning of the word, as they don’t meet the legal age requirements. For minors, consent is provided by parents or legal guardians, and this process of acquiring both consent and assent is called a dual consent procedure [1].

  1. Hein IM, De Vries MC, Troost PW, Meynen G, Van Goudoever JB, Lindauer RJ. Informed consent instead of assent is appropriate in children from the age of twelve: Policy implications of new findings on children's competence to consent to clinical research. BMC Med Ethics. 2015;16(1):015-0067.

Why is this important?

In order to conduct clinical research in an ethical manner, informed assent from children and informed consent from their legal guardians must be sought. Respecting both children’s wishes and asking parents’ permission is necessary in order to respect laws and rules of good clinical practice, and to respect patients’ autonomy, despite the fact that the patient is a minor [1].

  1. Poston RD. Assent Described: Exploring Perspectives From the Inside. J Pediatr Nurs. 2016;31(6):e353-e65.

For whom is this important?

Other information

Virtues & Values
Good Practices & Misconduct
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