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Under some circumstances, a verbal consent process may be more appropriate. In either case, the researcher must maintain a record of the process they followed when obtaining informed consent from each participant.
If you agree to participate in this study, you are giving us permission to collect, use and share your health information. If you decide not to verbally agree to allow for us to use and disclose your protected health information, you cannot be in the research study.
The researcher must document that oral consent was provided. This can be done via written field notes, audio or video recording or other available means. 6. Section 34(2) of the Health Information Act states that consent for the disclosure of personal health information must be written or electronic.
If the participant agrees to participate in the study, the participants oral/verbal consent should be recorded on an audio recorder or in the researchers notes.
Oral consent should be recorded by audio and stored with the information letter (if the participant has been provided with an information letter). If possible, send a copy of both the information letter and the audio recording to the participant.
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The evidence that can be used to prove consent include digital communication records, witness testimonies, and physical evidence. Digital communication records, such as text messages and emails, can provide context and intent, supporting claims of consensual sexual activity.

example of verbal consent in healthcare