When Oral Consent Will Do

Elisa J. Gordon

doi:10.1177/1525822X0001200304

When Oral Consent Will Do

Elisa J. Gordon^*

^*Corresponding author for this work

Surgery, Transplant Surgery Division

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

Abstract

Informed consent in research requires investigators to explain to potential participants the procedures, risks, benefits, and alternatives of a study through either oral or written consent. This article discusses cases when oral consent may be more appropriate to use than written consent. A proposal is presented for writing Institutional Review Board (IRB) protocols that incorporate both types of consent to protect the interests of participants and investigators.

Original language	English (US)
Pages (from-to)	235-238
Number of pages	4
Journal	Field Methods
Volume	12
Issue number	3
DOIs	https://doi.org/10.1177/1525822X0001200304
State	Published - Jan 1 2000

ASJC Scopus subject areas

Anthropology

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10.1177/1525822X0001200304

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title = "When Oral Consent Will Do",

abstract = "Informed consent in research requires investigators to explain to potential participants the procedures, risks, benefits, and alternatives of a study through either oral or written consent. This article discusses cases when oral consent may be more appropriate to use than written consent. A proposal is presented for writing Institutional Review Board (IRB) protocols that incorporate both types of consent to protect the interests of participants and investigators.",

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N2 - Informed consent in research requires investigators to explain to potential participants the procedures, risks, benefits, and alternatives of a study through either oral or written consent. This article discusses cases when oral consent may be more appropriate to use than written consent. A proposal is presented for writing Institutional Review Board (IRB) protocols that incorporate both types of consent to protect the interests of participants and investigators.

AB - Informed consent in research requires investigators to explain to potential participants the procedures, risks, benefits, and alternatives of a study through either oral or written consent. This article discusses cases when oral consent may be more appropriate to use than written consent. A proposal is presented for writing Institutional Review Board (IRB) protocols that incorporate both types of consent to protect the interests of participants and investigators.

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UR - https://www.scopus.com/inward/citedby.url?scp=84996198884&partnerID=8YFLogxK

U2 - 10.1177/1525822X0001200304

DO - 10.1177/1525822X0001200304

M3 - Article

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VL - 12

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JO - Field Methods

JF - Field Methods

IS - 3

ER -

When Oral Consent Will Do

Abstract

ASJC Scopus subject areas

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